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          "order": 280
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      "category": "structure",
      "mount_path": "/plugins/protein_evolution/",
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        "icon": "fa-history",
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      "engine": "nextflow",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Designs adaptive clinical trials including group-sequential (O'Brien-Fleming, Pocock, Lan-DeMets spending), sample-size re-estimation (blinded Friede-Kieser, unblinded Cui-Hung-Wang, Mehta-Pocock promising zone), seamless Phase 2/3 with treatment-arm selection, population enrichment, and response-ad",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "b57d7704-3b86-4bd0-9e21-97bacfdb199f",
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Designs adaptive clinical trials including group-sequential (O'Brien-Fleming, Pocock, Lan-DeMets spending), sample-size re-estimation (blinded Friede-Kieser, unblinded Cui-Hung-Wang, Mehta-Pocock promising zone), seamless Phase 2/3 with treatment-arm selection, population enrichment, and response-ad",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "b57d7704-3b86-4bd0-9e21-97bacfdb199f",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:55:56.661"
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      "id": 52,
      "workflow_bundle_id": "8493c102-9188-45df-b50d-92f29012c4ab",
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      "engine": "nextflow",
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      "display_name": "ADMET Property Prediction Pipeline",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Predict ADMET (Absorption, Distribution, Metabolism, Excretion, Toxicity) properties of drug candidates from SMILES input. Generates traffic-light visualization and detailed HTML report.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "8493c102-9188-45df-b50d-92f29012c4ab",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Predict ADMET (Absorption, Distribution, Metabolism, Excretion, Toxicity) properties of drug candidates from SMILES input. Generates traffic-light visualization and detailed HTML report.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "8493c102-9188-45df-b50d-92f29012c4ab",
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      "source": "workflow_registry",
      "id": 458,
      "workflow_bundle_id": "0f3be0c8-ea1e-41d6-aa35-ee87994ec4dd",
      "category": "clinical",
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      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Process multiple sequence files in batch using Biopython. Use when working with many files, merging/splitting sequences, or automating file operations across directories.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "0f3be0c8-ea1e-41d6-aa35-ee87994ec4dd",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:36.238",
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        "engine": "nextflow",
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        "display_name": "Batch Processing",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Process multiple sequence files in batch using Biopython. Use when working with many files, merging/splitting sequences, or automating file operations across directories.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "0f3be0c8-ea1e-41d6-aa35-ee87994ec4dd",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:36.238"
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    {
      "source": "workflow_registry",
      "id": 212,
      "workflow_bundle_id": "9d03aa03-ac1a-4c27-b970-83c65fa4489c",
      "category": "clinical",
      "engine": "nextflow",
      "name": "bayesian_trials",
      "display_name": "Bayesian Trials",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Designs Bayesian clinical trials including Phase I dose-finding (BOIN, CRM, EWOC, mTPI-2), meta-analytic-predictive (MAP) priors with robust mixtures for external data borrowing, EXNEX for basket trials, hierarchical models for safety AE (Berry-Berry), Bayesian platform trials (I-SPY 2, GBM AGILE, R",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "9d03aa03-ac1a-4c27-b970-83c65fa4489c",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:55:58.588",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "bayesian_trials",
        "display_name": "Bayesian Trials",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Designs Bayesian clinical trials including Phase I dose-finding (BOIN, CRM, EWOC, mTPI-2), meta-analytic-predictive (MAP) priors with robust mixtures for external data borrowing, EXNEX for basket trials, hierarchical models for safety AE (Berry-Berry), Bayesian platform trials (I-SPY 2, GBM AGILE, R",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "9d03aa03-ac1a-4c27-b970-83c65fa4489c",
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        "created_by": "manish",
        "created_at": "2026-06-08T01:55:58.588"
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      "source": "workflow_registry",
      "id": 433,
      "workflow_bundle_id": "e116ad6c-e9ed-4c4e-9f14-b8a07463aa31",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "Bowtie2 Alignment",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Align short reads using Bowtie2 with local or end-to-end modes. Supports gapped alignment. Use when aligning ChIP-seq, ATAC-seq, or when flexible alignment modes are needed.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "e116ad6c-e9ed-4c4e-9f14-b8a07463aa31",
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      "created_by": "manish",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "bowtie2_alignment",
        "display_name": "Bowtie2 Alignment",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Align short reads using Bowtie2 with local or end-to-end modes. Supports gapped alignment. Use when aligning ChIP-seq, ATAC-seq, or when flexible alignment modes are needed.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "e116ad6c-e9ed-4c4e-9f14-b8a07463aa31",
        "enabled": 1,
        "created_by": "manish",
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      "id": 434,
      "workflow_bundle_id": "1144b0d7-ec91-4a74-a9d6-57cc6476bf91",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "Bwa Alignment",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Align DNA short reads to reference genomes using bwa-mem2, the faster successor to BWA-MEM. Use when aligning DNA short reads to a reference genome.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "1144b0d7-ec91-4a74-a9d6-57cc6476bf91",
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      "created_by": "manish",
      "created_at": "2026-06-08T02:02:52.715",
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        "display_name": "Bwa Alignment",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Align DNA short reads to reference genomes using bwa-mem2, the faster successor to BWA-MEM. Use when aligning DNA short reads to a reference genome.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "1144b0d7-ec91-4a74-a9d6-57cc6476bf91",
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        "created_by": "manish",
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      "workflow_bundle_id": "b25fd0aa-27cc-43de-9465-04d8fe17df50",
      "category": "clinical",
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      "display_name": "Categorical Tests",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Tests associations between categorical variables in clinical data using chi-square, Fisher's exact, Boschloo, Cochran-Mantel-Haenszel, and modern McNemar variants with calibrated confidence intervals (Wilson, Newcombe, Miettinen-Nurminen). Use when analyzing categorical outcomes, paired binary endpo",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "b25fd0aa-27cc-43de-9465-04d8fe17df50",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:56:00.456",
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Tests associations between categorical variables in clinical data using chi-square, Fisher's exact, Boschloo, Cochran-Mantel-Haenszel, and modern McNemar variants with calibrated confidence intervals (Wilson, Newcombe, Miettinen-Nurminen). Use when analyzing categorical outcomes, paired binary endpo",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "b25fd0aa-27cc-43de-9465-04d8fe17df50",
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        "created_by": "manish",
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      "id": 214,
      "workflow_bundle_id": "d3631778-07cc-41f0-9841-b158762e063c",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "Cdisc Data Handling",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Reads, validates, and prepares CDISC SDTM and ADaM clinical trial data for analysis. Covers SDTM domain joins (DM, AE, EX, VS, LB, DS), ADaM architecture (ADSL, BDS, OCCDS, ADTTE) with traceability, treatment-emergent AE conventions, baseline derivation, SUPPQUAL/NSV handling, Define-XML 2.1, and Pi",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d3631778-07cc-41f0-9841-b158762e063c",
      "enabled": 1,
      "created_by": "manish",
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        "engine": "nextflow",
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Reads, validates, and prepares CDISC SDTM and ADaM clinical trial data for analysis. Covers SDTM domain joins (DM, AE, EX, VS, LB, DS), ADaM architecture (ADSL, BDS, OCCDS, ADTTE) with traceability, treatment-emergent AE conventions, baseline derivation, SUPPQUAL/NSV handling, Define-XML 2.1, and Pi",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d3631778-07cc-41f0-9841-b158762e063c",
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        "created_by": "manish",
        "created_at": "2026-06-08T01:56:02.235"
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      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "Cell Segmentation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Segment single cells from multiplexed IMC/MIBI tissue images using Mesmer/DeepCell, Cellpose, or ilastik+CellProfiler, covering whole-cell vs nuclear segmentation, the summed-membrane-channel decision, nuclear-expansion bias, lateral spillover, resolution-floor parameters, and downstream-proxy evalu",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "ec0d1da9-822c-45f3-8368-892bae1ea7a8",
      "enabled": 1,
      "created_by": "manish",
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        "engine": "nextflow",
        "name": "cell_segmentation",
        "display_name": "Cell Segmentation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Segment single cells from multiplexed IMC/MIBI tissue images using Mesmer/DeepCell, Cellpose, or ilastik+CellProfiler, covering whole-cell vs nuclear segmentation, the summed-membrane-channel decision, nuclear-expansion bias, lateral spillover, resolution-floor parameters, and downstream-proxy evalu",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "ec0d1da9-822c-45f3-8368-892bae1ea7a8",
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        "created_by": "manish",
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    {
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      "id": 150,
      "workflow_bundle_id": "546d7ef5-89aa-4710-a263-949d6eba4fda",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "cfDNA Fragment Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "cfDNA fragment analysis with FinaleToolkit coverage, DELFI scoring, and summary statistics",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "546d7ef5-89aa-4710-a263-949d6eba4fda",
      "enabled": 1,
      "created_by": "manish",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "cfdna_fragment",
        "display_name": "cfDNA Fragment Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "cfDNA fragment analysis with FinaleToolkit coverage, DELFI scoring, and summary statistics",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "546d7ef5-89aa-4710-a263-949d6eba4fda",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:48:23.508"
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    {
      "source": "workflow_registry",
      "id": 102,
      "workflow_bundle_id": "559adf64-49f1-4c42-b228-740703908c8f",
      "category": "clinical",
      "engine": "nextflow",
      "name": "cfdna_liquid_biopsy",
      "display_name": "cfDNA Liquid Biopsy",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "ichorCNA and DELFI fragmentomics copy number analysis from cell-free DNA",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": "docker.io/man4ish/omnibioai-purple:1.0",
      "object_id": "559adf64-49f1-4c42-b228-740703908c8f",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-05T23:05:18.524",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "cfdna_liquid_biopsy",
        "display_name": "cfDNA Liquid Biopsy",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "ichorCNA and DELFI fragmentomics copy number analysis from cell-free DNA",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-purple:1.0",
        "object_id": "559adf64-49f1-4c42-b228-740703908c8f",
        "enabled": 1,
        "created_by": "manish",
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      "id": 362,
      "workflow_bundle_id": "e28281f3-6e5a-4eee-8726-534ade99aa93",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "Cfdna Preprocessing",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Preprocesses cell-free DNA sequencing data including adapter trimming, alignment optimized for short fragments, and UMI-aware duplicate removal using fgbio. Applies cfDNA-specific quality thresholds and fragment length filtering. Use when processing plasma cfDNA sequencing data before downstream ana",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "e28281f3-6e5a-4eee-8726-534ade99aa93",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:00:35.549",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
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        "display_name": "Cfdna Preprocessing",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Preprocesses cell-free DNA sequencing data including adapter trimming, alignment optimized for short fragments, and UMI-aware duplicate removal using fgbio. Applies cfDNA-specific quality thresholds and fragment length filtering. Use when processing plasma cfDNA sequencing data before downstream ana",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "e28281f3-6e5a-4eee-8726-534ade99aa93",
        "enabled": 1,
        "created_by": "manish",
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      "source": "workflow_registry",
      "id": 500,
      "workflow_bundle_id": "dad016a8-82de-4d52-a671-5cc41e27f523",
      "category": "clinical",
      "engine": "nextflow",
      "name": "clinical_interpretation",
      "display_name": "Clinical Interpretation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Clinical variant interpretation using ClinVar, ACMG guidelines, and pathogenicity predictors. Prioritize variants for diagnostic and research applications. Use when interpreting clinical significance of variants.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "dad016a8-82de-4d52-a671-5cc41e27f523",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:04:53.221",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "clinical_interpretation",
        "display_name": "Clinical Interpretation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Clinical variant interpretation using ClinVar, ACMG guidelines, and pathogenicity predictors. Prioritize variants for diagnostic and research applications. Use when interpreting clinical significance of variants.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "dad016a8-82de-4d52-a671-5cc41e27f523",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:04:53.221"
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    {
      "source": "workflow_registry",
      "id": 53,
      "workflow_bundle_id": "6aaf24ba-b67d-4ed5-9e71-211eaa344437",
      "category": "clinical",
      "engine": "nextflow",
      "name": "clinical_trial_matching_v1",
      "display_name": "Clinical Trial Matching Pipeline",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Match patients to clinical trials based on genomic biomarkers and clinical eligibility criteria. Generates ranked trial matches with full eligibility breakdown.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "6aaf24ba-b67d-4ed5-9e71-211eaa344437",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-22T07:26:06.444",
      "raw": {
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        "engine": "nextflow",
        "name": "clinical_trial_matching_v1",
        "display_name": "Clinical Trial Matching Pipeline",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Match patients to clinical trials based on genomic biomarkers and clinical eligibility criteria. Generates ranked trial matches with full eligibility breakdown.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "6aaf24ba-b67d-4ed5-9e71-211eaa344437",
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        "created_by": "manish",
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    {
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      "workflow_bundle_id": "194161cd-0a5a-4324-bc90-b707d693fb14",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "CNV Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "GATK somatic CNV and CNVkit circular binary segmentation for copy number alterations",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": "docker.io/man4ish/omnibioai-clinical:1.0",
      "object_id": "194161cd-0a5a-4324-bc90-b707d693fb14",
      "enabled": 1,
      "created_by": "manish",
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      "raw": {
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        "category": "clinical",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "GATK somatic CNV and CNVkit circular binary segmentation for copy number alterations",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-clinical:1.0",
        "object_id": "194161cd-0a5a-4324-bc90-b707d693fb14",
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        "created_by": "manish",
        "created_at": "2026-06-05T23:05:08.069"
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    {
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      "workflow_bundle_id": "c766dbbd-5978-45ba-bfbc-1a3e50a38f56",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "CNVkit Copy Number Analysis",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "CNVkit copy number analysis with batch processing, scatter plot, and copy number calling",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "c766dbbd-5978-45ba-bfbc-1a3e50a38f56",
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      "created_by": "manish",
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      "raw": {
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "CNVkit copy number analysis with batch processing, scatter plot, and copy number calling",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c766dbbd-5978-45ba-bfbc-1a3e50a38f56",
        "enabled": 1,
        "created_by": "manish",
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    {
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      "workflow_bundle_id": "c2a9fba6-0db7-4319-b5e7-46682093407a",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "Codon Usage",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Analyze codon usage, calculate CAI (Codon Adaptation Index), and examine synonymous codon bias using Biopython. Use when analyzing coding sequences for expression optimization or evolutionary analysis.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "c2a9fba6-0db7-4319-b5e7-46682093407a",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:52.746",
      "raw": {
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        "engine": "nextflow",
        "name": "codon_usage",
        "display_name": "Codon Usage",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Analyze codon usage, calculate CAI (Codon Adaptation Index), and examine synonymous codon bias using Biopython. Use when analyzing coding sequences for expression optimization or evolutionary analysis.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c2a9fba6-0db7-4319-b5e7-46682093407a",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:52.746"
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      "id": 635,
      "workflow_bundle_id": "1ce3a729-781a-42d6-b767-678010f93f73",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "Colocalization Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Test colocalization of GWAS and eQTL signals at shared loci using the coloc Bayesian framework.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "1ce3a729-781a-42d6-b767-678010f93f73",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:44:43.831",
      "raw": {
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        "engine": "nextflow",
        "name": "coloc_colocalization",
        "display_name": "Colocalization Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Test colocalization of GWAS and eQTL signals at shared loci using the coloc Bayesian framework.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "1ce3a729-781a-42d6-b767-678010f93f73",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:44:43.831"
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    {
      "source": "workflow_registry",
      "id": 459,
      "workflow_bundle_id": "a992b0c1-c805-49bd-9b49-d89f7fbf55ab",
      "category": "clinical",
      "engine": "nextflow",
      "name": "compressed_files",
      "display_name": "Compressed Files",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Read and write compressed sequence files (gzip, bzip2, BGZF) using Biopython. Use when working with .gz or .bz2 sequence files. Use BGZF for indexable compressed files.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "a992b0c1-c805-49bd-9b49-d89f7fbf55ab",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:38.173",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "compressed_files",
        "display_name": "Compressed Files",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Read and write compressed sequence files (gzip, bzip2, BGZF) using Biopython. Use when working with .gz or .bz2 sequence files. Use BGZF for indexable compressed files.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "a992b0c1-c805-49bd-9b49-d89f7fbf55ab",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:38.173"
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      "id": 501,
      "workflow_bundle_id": "c7041d91-d904-4539-9b00-2222bf618011",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "Consensus Sequences",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Generate consensus FASTA sequences by applying VCF variants to a reference using bcftools consensus. Use when creating sample-specific reference sequences or reconstructing haplotypes.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "c7041d91-d904-4539-9b00-2222bf618011",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:04:55.085",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "consensus_sequences",
        "display_name": "Consensus Sequences",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Generate consensus FASTA sequences by applying VCF variants to a reference using bcftools consensus. Use when creating sample-specific reference sequences or reconstructing haplotypes.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c7041d91-d904-4539-9b00-2222bf618011",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:04:55.085"
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      "source": "workflow_registry",
      "id": 438,
      "workflow_bundle_id": "5bf5ce55-f5fd-470d-949c-05972a5f1abb",
      "category": "clinical",
      "engine": "nextflow",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Detect sample contamination and cross-species reads using FastQ Screen. Screen reads against multiple reference genomes to identify bacterial, viral, adapter, or sample swap contamination. Use when suspecting cross-contamination or working with samples prone to microbial contamination.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "5bf5ce55-f5fd-470d-949c-05972a5f1abb",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:00.121",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
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        "display_name": "Contamination Screening",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Detect sample contamination and cross-species reads using FastQ Screen. Screen reads against multiple reference genomes to identify bacterial, viral, adapter, or sample swap contamination. Use when suspecting cross-contamination or working with samples prone to microbial contamination.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "5bf5ce55-f5fd-470d-949c-05972a5f1abb",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:00.121"
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      "id": 248,
      "workflow_bundle_id": "6cc7585b-4fe8-4683-8501-fc44497a11e4",
      "category": "clinical",
      "engine": "nextflow",
      "name": "copy_number_allele_specific_copy_number",
      "display_name": "Copy Number Allele Specific Copy Number",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Infer integer allele-specific copy number, tumor purity, and ploidy from tumor sequencing by jointly modeling read depth (logR) and B-allele frequency (BAF) with ASCAT, Sequenza, FACETS, PURPLE, and PureCN (tumor-only). Covers the purity-ploidy identifiability problem, the diploid-baseline (dipLogR)",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "6cc7585b-4fe8-4683-8501-fc44497a11e4",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:04.387",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "copy_number_allele_specific_copy_number",
        "display_name": "Copy Number Allele Specific Copy Number",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Infer integer allele-specific copy number, tumor purity, and ploidy from tumor sequencing by jointly modeling read depth (logR) and B-allele frequency (BAF) with ASCAT, Sequenza, FACETS, PURPLE, and PureCN (tumor-only). Covers the purity-ploidy identifiability problem, the diploid-baseline (dipLogR)",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "6cc7585b-4fe8-4683-8501-fc44497a11e4",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:57:04.387"
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    {
      "source": "workflow_registry",
      "id": 249,
      "workflow_bundle_id": "4321e803-91f2-47d9-8b56-241342e1c7c2",
      "category": "clinical",
      "engine": "nextflow",
      "name": "copy_number_cnv_annotation",
      "display_name": "Copy Number CNV Annotation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Annotate copy number variant segments with overlapping genes, dosage-sensitivity scores, cancer driver databases, population frequencies, and clinical-variant content. Covers bedtools/pybedtools interval intersection, AnnotSV comprehensive annotation and ranking, ClinGen haploinsufficiency/triplosen",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "4321e803-91f2-47d9-8b56-241342e1c7c2",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:06.244",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "copy_number_cnv_annotation",
        "display_name": "Copy Number CNV Annotation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Annotate copy number variant segments with overlapping genes, dosage-sensitivity scores, cancer driver databases, population frequencies, and clinical-variant content. Covers bedtools/pybedtools interval intersection, AnnotSV comprehensive annotation and ranking, ClinGen haploinsufficiency/triplosen",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "4321e803-91f2-47d9-8b56-241342e1c7c2",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:57:06.244"
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    {
      "source": "workflow_registry",
      "id": 250,
      "workflow_bundle_id": "cad3722b-dc62-45f6-aeb7-53b424257b2d",
      "category": "clinical",
      "engine": "nextflow",
      "name": "copy_number_cnv_visualization",
      "display_name": "Copy Number CNV Visualization",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Visualize copy number profiles, segments, allele-specific tracks, and cohort patterns from CNVkit, GATK, ASCAT, FACETS, Sequenza, and other callers. Covers genome-wide and per-chromosome log2 scatter plots, B-allele-frequency/minor-allele-fraction tracks, ideograms, cohort heatmaps, circos views, an",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "cad3722b-dc62-45f6-aeb7-53b424257b2d",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:08.124",
      "raw": {
        "id": 250,
        "category": "clinical",
        "engine": "nextflow",
        "name": "copy_number_cnv_visualization",
        "display_name": "Copy Number CNV Visualization",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Visualize copy number profiles, segments, allele-specific tracks, and cohort patterns from CNVkit, GATK, ASCAT, FACETS, Sequenza, and other callers. Covers genome-wide and per-chromosome log2 scatter plots, B-allele-frequency/minor-allele-fraction tracks, ideograms, cohort heatmaps, circos views, an",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "cad3722b-dc62-45f6-aeb7-53b424257b2d",
        "enabled": 1,
        "created_by": "manish",
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    {
      "source": "workflow_registry",
      "id": 251,
      "workflow_bundle_id": "985568d0-2952-4a26-9664-2ea55d43af9d",
      "category": "clinical",
      "engine": "nextflow",
      "name": "copy_number_cnvkit_analysis",
      "display_name": "Copy Number Cnvkit Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Detect somatic and germline copy number variants from targeted, exome, and whole-genome sequencing with CNVkit, a read-depth caller that combines on-target and off-target (antitarget) coverage. Covers panel-of-normals construction, flat-reference tumor-only calling, hybrid/amplicon/WGS modes, CBS vs",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "985568d0-2952-4a26-9664-2ea55d43af9d",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:09.963",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "copy_number_cnvkit_analysis",
        "display_name": "Copy Number Cnvkit Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Detect somatic and germline copy number variants from targeted, exome, and whole-genome sequencing with CNVkit, a read-depth caller that combines on-target and off-target (antitarget) coverage. Covers panel-of-normals construction, flat-reference tumor-only calling, hybrid/amplicon/WGS modes, CBS vs",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "985568d0-2952-4a26-9664-2ea55d43af9d",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:57:09.963"
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    {
      "source": "workflow_registry",
      "id": 252,
      "workflow_bundle_id": "3d1903ac-8104-45cb-b3cf-744b6ff43f63",
      "category": "clinical",
      "engine": "nextflow",
      "name": "copy_number_copy_ratio_segmentation",
      "display_name": "Copy Number Copy Ratio Segmentation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Normalize read-depth copy-ratio profiles and segment them into copy-number regions using circular binary segmentation (CBS, DNAcopy), hidden Markov models, HaarSeg, and fused-lasso methods. Covers GC-content, mappability, and replication-timing (wave-artifact) bias correction, panel-of-normals/PCA d",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "3d1903ac-8104-45cb-b3cf-744b6ff43f63",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:11.830",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "copy_number_copy_ratio_segmentation",
        "display_name": "Copy Number Copy Ratio Segmentation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Normalize read-depth copy-ratio profiles and segment them into copy-number regions using circular binary segmentation (CBS, DNAcopy), hidden Markov models, HaarSeg, and fused-lasso methods. Covers GC-content, mappability, and replication-timing (wave-artifact) bias correction, panel-of-normals/PCA d",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "3d1903ac-8104-45cb-b3cf-744b6ff43f63",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:57:11.830"
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    {
      "source": "workflow_registry",
      "id": 253,
      "workflow_bundle_id": "c909b379-40d3-4f38-b2ee-f519f8a1031b",
      "category": "clinical",
      "engine": "nextflow",
      "name": "copy_number_focal_amplification_ecdna",
      "display_name": "Copy Number Focal Amplification Ecdna",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Resolve the architecture of focal oncogene amplifications \u2014 extrachromosomal DNA (ecDNA), breakage-fusion-bridge (BFB) cycles, homogeneously staining regions (HSR), and linear amplification \u2014 from whole-genome sequencing with AmpliconArchitect, the AmpliconSuite pipeline, and AmpliconClassifier. Cov",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "c909b379-40d3-4f38-b2ee-f519f8a1031b",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:13.691",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "copy_number_focal_amplification_ecdna",
        "display_name": "Copy Number Focal Amplification Ecdna",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Resolve the architecture of focal oncogene amplifications \u2014 extrachromosomal DNA (ecDNA), breakage-fusion-bridge (BFB) cycles, homogeneously staining regions (HSR), and linear amplification \u2014 from whole-genome sequencing with AmpliconArchitect, the AmpliconSuite pipeline, and AmpliconClassifier. Cov",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c909b379-40d3-4f38-b2ee-f519f8a1031b",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:57:13.691"
      }
    },
    {
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      "engine": "nextflow",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Call copy number variants with the GATK best-practices workflows \u2014 the somatic CNV pipeline (CollectReadCounts, DenoiseReadCounts with tangent normalization, ModelSegments, CallCopyRatioSegments) and the germline GATK-gCNV pipeline (DetermineGermlineContigPloidy, GermlineCNVCaller cohort/case mode, ",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "e3089929-3911-4cc1-934d-c9242fac9e53",
      "enabled": 1,
      "created_by": "manish",
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        "display_name": "Copy Number Gatk CNV",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "e3089929-3911-4cc1-934d-c9242fac9e53",
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        "created_by": "manish",
        "created_at": "2026-06-08T01:57:15.547"
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      "source": "workflow_registry",
      "id": 255,
      "workflow_bundle_id": "6d591356-9a84-481c-8371-b7429c4dd50b",
      "category": "clinical",
      "engine": "nextflow",
      "name": "copy_number_germline_cnv_interpretation",
      "display_name": "Copy Number Germline CNV Interpretation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Classify constitutional (germline) copy number variants for clinical reporting using the 2019 ACMG/ClinGen technical standards points-based framework, with ClassifyCNV and AnnotSV for semi-automated scoring. Covers the separate copy-number-loss and copy-number-gain rubrics, the five-tier classificat",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "6d591356-9a84-481c-8371-b7429c4dd50b",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:17.391",
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        "engine": "nextflow",
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "6d591356-9a84-481c-8371-b7429c4dd50b",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:57:17.391"
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      "source": "workflow_registry",
      "id": 256,
      "workflow_bundle_id": "d6d17be8-a766-4147-9977-0128a2713886",
      "category": "clinical",
      "engine": "nextflow",
      "name": "copy_number_hrd_scoring",
      "display_name": "Copy Number Hrd Scoring",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Quantify homologous recombination deficiency (HRD) from tumor copy number using the three genomic-scar metrics \u2014 loss of heterozygosity (LOH), large-scale state transitions (LST), and telomeric allelic imbalance (TAI) \u2014 with scarHRD, and via the whole-genome HRDetect and CHORD models. Covers the gen",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d6d17be8-a766-4147-9977-0128a2713886",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:19.237",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "copy_number_hrd_scoring",
        "display_name": "Copy Number Hrd Scoring",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
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        "description": "Quantify homologous recombination deficiency (HRD) from tumor copy number using the three genomic-scar metrics \u2014 loss of heterozygosity (LOH), large-scale state transitions (LST), and telomeric allelic imbalance (TAI) \u2014 with scarHRD, and via the whole-genome HRDetect and CHORD models. Covers the gen",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d6d17be8-a766-4147-9977-0128a2713886",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:57:19.237"
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    {
      "source": "workflow_registry",
      "id": 257,
      "workflow_bundle_id": "58748330-b8a0-48ae-ad1b-b80c952c067c",
      "category": "clinical",
      "engine": "nextflow",
      "name": "copy_number_recurrent_cnv",
      "display_name": "Copy Number Recurrent CNV",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Identify recurrent and driver copy number alterations across a tumor cohort with GISTIC2 (G-score, Ziggurat deconstruction, focal vs broad/arm-level analysis, q-values from permutation) and quantify copy-number signatures with the Steele 2022 COSMIC framework and the Drews 2022 CINSignatures framewo",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "58748330-b8a0-48ae-ad1b-b80c952c067c",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:21.084",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "copy_number_recurrent_cnv",
        "display_name": "Copy Number Recurrent CNV",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Identify recurrent and driver copy number alterations across a tumor cohort with GISTIC2 (G-score, Ziggurat deconstruction, focal vs broad/arm-level analysis, q-values from permutation) and quantify copy-number signatures with the Steele 2022 COSMIC framework and the Drews 2022 CINSignatures framewo",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "58748330-b8a0-48ae-ad1b-b80c952c067c",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:57:21.084"
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    {
      "source": "workflow_registry",
      "id": 258,
      "workflow_bundle_id": "742f0b47-8cdd-4559-90a2-ff1c59b2e6bb",
      "category": "clinical",
      "engine": "nextflow",
      "name": "copy_number_subclonal_copy_number",
      "display_name": "Copy Number Subclonal Copy Number",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Resolve subclonal copy number, whole-genome doubling, and copy-number tumor evolution from bulk sequencing with Battenberg, TITAN, and MEDICC2. Covers clonal versus subclonal copy-number states, haplotype phasing for subclonal resolution, cancer cell fraction, whole-genome-doubling detection and tim",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "742f0b47-8cdd-4559-90a2-ff1c59b2e6bb",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:22.919",
      "raw": {
        "id": 258,
        "category": "clinical",
        "engine": "nextflow",
        "name": "copy_number_subclonal_copy_number",
        "display_name": "Copy Number Subclonal Copy Number",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Resolve subclonal copy number, whole-genome doubling, and copy-number tumor evolution from bulk sequencing with Battenberg, TITAN, and MEDICC2. Covers clonal versus subclonal copy-number states, haplotype phasing for subclonal resolution, cancer cell fraction, whole-genome-doubling detection and tim",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "742f0b47-8cdd-4559-90a2-ff1c59b2e6bb",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:57:22.919"
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      "source": "workflow_registry",
      "id": 68,
      "workflow_bundle_id": "3afdad8f-176b-41a2-bb3a-04352865165e",
      "category": "clinical",
      "engine": "nextflow",
      "name": "ctdna_analysis_v1",
      "display_name": "ctDNA Liquid Biopsy",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Circulating tumor DNA (ctDNA) liquid biopsy pipeline for tumor fraction estimation, somatic variant calling, CNV profiling, and tissue-of-origin prediction.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "3afdad8f-176b-41a2-bb3a-04352865165e",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-22T21:55:26.171",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "ctdna_analysis_v1",
        "display_name": "ctDNA Liquid Biopsy",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Circulating tumor DNA (ctDNA) liquid biopsy pipeline for tumor fraction estimation, somatic variant calling, CNV profiling, and tissue-of-origin prediction.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "3afdad8f-176b-41a2-bb3a-04352865165e",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-05-22T21:55:26.171"
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    {
      "source": "workflow_registry",
      "id": 149,
      "workflow_bundle_id": "ab35a501-47bb-413c-a6c1-12693a9ee8a9",
      "category": "clinical",
      "engine": "nextflow",
      "name": "ctdna_mutation",
      "display_name": "ctDNA Mutation Detection",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "ctDNA mutation detection with VarDict and low-VAF variant filtering",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "ab35a501-47bb-413c-a6c1-12693a9ee8a9",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:48:21.718",
      "raw": {
        "id": 149,
        "category": "clinical",
        "engine": "nextflow",
        "name": "ctdna_mutation",
        "display_name": "ctDNA Mutation Detection",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "ctDNA mutation detection with VarDict and low-VAF variant filtering",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "ab35a501-47bb-413c-a6c1-12693a9ee8a9",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:48:21.718"
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    {
      "source": "workflow_registry",
      "id": 363,
      "workflow_bundle_id": "bdfcd297-e99c-4936-b702-f1364f3c9981",
      "category": "clinical",
      "engine": "nextflow",
      "name": "ctdna_mutation_detection",
      "display_name": "Ctdna Mutation Detection",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Detects somatic mutations in circulating tumor DNA using variant callers optimized for low allele fractions with UMI-based error suppression. Reliably detects mutations at VAF above 0.5 percent using consensus-based approaches. Use when identifying tumor mutations from plasma DNA or tracking specifi",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "bdfcd297-e99c-4936-b702-f1364f3c9981",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:00:37.407",
      "raw": {
        "id": 363,
        "category": "clinical",
        "engine": "nextflow",
        "name": "ctdna_mutation_detection",
        "display_name": "Ctdna Mutation Detection",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Detects somatic mutations in circulating tumor DNA using variant callers optimized for low allele fractions with UMI-based error suppression. Reliably detects mutations at VAF above 0.5 percent using consensus-based approaches. Use when identifying tumor mutations from plasma DNA or tracking specifi",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "bdfcd297-e99c-4936-b702-f1364f3c9981",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:00:37.407"
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    {
      "source": "workflow_registry",
      "id": 352,
      "workflow_bundle_id": "c499506d-34dd-42bd-bc4c-df6fc9368879",
      "category": "clinical",
      "engine": "nextflow",
      "name": "data_preprocessing",
      "display_name": "Data Preprocessing",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Load and preprocess imaging mass cytometry (IMC) and MIBI data from raw MCD/TXT through hot-pixel removal, spillover compensation, and variance-stabilizing transformation, covering readimc/steinbock ingestion, NNLS spillover compensation (CATALYST), IMC-Denoise, and the IMC arcsinh-cofactor question",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "c499506d-34dd-42bd-bc4c-df6fc9368879",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:00:15.247",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "data_preprocessing",
        "display_name": "Data Preprocessing",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Load and preprocess imaging mass cytometry (IMC) and MIBI data from raw MCD/TXT through hot-pixel removal, spillover compensation, and variance-stabilizing transformation, covering readimc/steinbock ingestion, NNLS spillover compensation (CATALYST), IMC-Denoise, and the IMC arcsinh-cofactor question",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c499506d-34dd-42bd-bc4c-df6fc9368879",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:00:15.247"
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    {
      "source": "workflow_registry",
      "id": 502,
      "workflow_bundle_id": "43e70d9d-3dc0-4e9c-bb8e-02410e434603",
      "category": "clinical",
      "engine": "nextflow",
      "name": "deepvariant",
      "display_name": "Deepvariant",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Deep learning-based variant calling with Google DeepVariant. Provides high accuracy for germline SNPs and indels from Illumina, PacBio, and ONT data. Use when calling variants with DeepVariant deep learning caller or when highest germline calling accuracy is required.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "43e70d9d-3dc0-4e9c-bb8e-02410e434603",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:04:57.028",
      "raw": {
        "id": 502,
        "category": "clinical",
        "engine": "nextflow",
        "name": "deepvariant",
        "display_name": "Deepvariant",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Deep learning-based variant calling with Google DeepVariant. Provides high accuracy for germline SNPs and indels from Illumina, PacBio, and ONT data. Use when calling variants with DeepVariant deep learning caller or when highest germline calling accuracy is required.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "43e70d9d-3dc0-4e9c-bb8e-02410e434603",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:04:57.028"
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    {
      "source": "workflow_registry",
      "id": 353,
      "workflow_bundle_id": "beaa0d1a-8d3b-42b0-ab47-0c640514947a",
      "category": "clinical",
      "engine": "nextflow",
      "name": "differential_analysis",
      "display_name": "Differential Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Compare cell-type composition and spatial features across conditions in IMC/MIBI cohorts with the patient as the experimental unit, covering pseudoreplication, per-patient aggregation, mixed models, compositional (Dirichlet/scCODA) differential abundance, diffcyt, per-image-to-patient spatial differ",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "beaa0d1a-8d3b-42b0-ab47-0c640514947a",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:00:17.043",
      "raw": {
        "id": 353,
        "category": "clinical",
        "engine": "nextflow",
        "name": "differential_analysis",
        "display_name": "Differential Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Compare cell-type composition and spatial features across conditions in IMC/MIBI cohorts with the patient as the experimental unit, covering pseudoreplication, per-patient aggregation, mixed models, compositional (Dirichlet/scCODA) differential abundance, diffcyt, per-image-to-patient spatial differ",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "beaa0d1a-8d3b-42b0-ab47-0c640514947a",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:00:17.043"
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    {
      "source": "workflow_registry",
      "id": 50,
      "workflow_bundle_id": "35b474e9-12e3-41e5-9d07-9aef4a76060a",
      "category": "clinical",
      "engine": "nextflow",
      "name": "drug_response_prediction_v1",
      "display_name": "Drug Response Prediction Pipeline",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Predict drug response (IC50/AUC) using genomic features: expression, mutations, and CNVs. Uses XGBoost cross-validated regression with feature importance analysis.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "35b474e9-12e3-41e5-9d07-9aef4a76060a",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-22T07:25:58.299",
      "raw": {
        "id": 50,
        "category": "clinical",
        "engine": "nextflow",
        "name": "drug_response_prediction_v1",
        "display_name": "Drug Response Prediction Pipeline",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Predict drug response (IC50/AUC) using genomic features: expression, mutations, and CNVs. Uses XGBoost cross-validated regression with feature importance analysis.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "35b474e9-12e3-41e5-9d07-9aef4a76060a",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-05-22T07:25:58.299"
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    {
      "source": "workflow_registry",
      "id": 72,
      "workflow_bundle_id": "6935e819-1d83-43cd-ac0a-d5ce0d09eadf",
      "category": "clinical",
      "engine": "nextflow",
      "name": "drug_synergy_v1",
      "display_name": "Drug Combination Synergy Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Drug combination screening pipeline for synergy/antagonism prediction using Bliss independence, HSA, and Loewe additivity models with response surface fitting.",
      "inputs_schema": "{\"model\": {\"type\": \"string\", \"description\": \"Synergy model (bliss/hsa/loewe)\"}, \"drug_a\": {\"type\": \"string\", \"description\": \"Drug A name\"}, \"drug_b\": {\"type\": \"string\", \"description\": \"Drug B name\"}, \"outdir\": {\"type\": \"string\", \"description\": \"Output directory\"}, \"cell_line\": {\"type\": \"string\", \"description\": \"Cell line identifier\"}, \"dose_response\": {\"type\": \"string\", \"description\": \"Dose-response matrix CSV\"}}",
      "outputs": "[\"synergy_scores.csv\", \"classification.json\", \"drug_synergy_report.html\"]",
      "container_image": null,
      "object_id": "6935e819-1d83-43cd-ac0a-d5ce0d09eadf",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-23T00:16:21.594",
      "raw": {
        "id": 72,
        "category": "clinical",
        "engine": "nextflow",
        "name": "drug_synergy_v1",
        "display_name": "Drug Combination Synergy Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Drug combination screening pipeline for synergy/antagonism prediction using Bliss independence, HSA, and Loewe additivity models with response surface fitting.",
        "inputs_schema": "{\"model\": {\"type\": \"string\", \"description\": \"Synergy model (bliss/hsa/loewe)\"}, \"drug_a\": {\"type\": \"string\", \"description\": \"Drug A name\"}, \"drug_b\": {\"type\": \"string\", \"description\": \"Drug B name\"}, \"outdir\": {\"type\": \"string\", \"description\": \"Output directory\"}, \"cell_line\": {\"type\": \"string\", \"description\": \"Cell line identifier\"}, \"dose_response\": {\"type\": \"string\", \"description\": \"Dose-response matrix CSV\"}}",
        "outputs": "[\"synergy_scores.csv\", \"classification.json\", \"drug_synergy_report.html\"]",
        "container_image": null,
        "object_id": "6935e819-1d83-43cd-ac0a-d5ce0d09eadf",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-05-23T00:16:21.594"
      }
    },
    {
      "source": "workflow_registry",
      "id": 215,
      "workflow_bundle_id": "5c4b7473-424d-4a87-84f8-a9e07c9c8ae4",
      "category": "clinical",
      "engine": "nextflow",
      "name": "effect_measures",
      "display_name": "Effect Measures",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Computes and interprets treatment effect measures (OR, RR, RD, HR, NNT) with calibrated confidence intervals (Wilson, Newcombe, Miettinen-Nurminen, MOVER, profile likelihood, Bender NNT) and reports marginal vs conditional estimands per FDA 2023 covariate adjustment guidance. Use when reporting trea",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "5c4b7473-424d-4a87-84f8-a9e07c9c8ae4",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:56:04.073",
      "raw": {
        "id": 215,
        "category": "clinical",
        "engine": "nextflow",
        "name": "effect_measures",
        "display_name": "Effect Measures",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Computes and interprets treatment effect measures (OR, RR, RD, HR, NNT) with calibrated confidence intervals (Wilson, Newcombe, Miettinen-Nurminen, MOVER, profile likelihood, Bender NNT) and reports marginal vs conditional estimands per FDA 2023 covariate adjustment guidance. Use when reporting trea",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "5c4b7473-424d-4a87-84f8-a9e07c9c8ae4",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:56:04.073"
      }
    },
    {
      "source": "workflow_registry",
      "id": 405,
      "workflow_bundle_id": "139c7c4f-1db3-4668-bebb-fd84b604aa7c",
      "category": "clinical",
      "engine": "nextflow",
      "name": "enrichment_visualization",
      "display_name": "Enrichment Visualization",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Visualize enrichment results using enrichplot package functions. Use when creating publication-quality figures from clusterProfiler results. Covers dotplot, barplot, cnetplot, emapplot, gseaplot2, ridgeplot, and treeplot.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "139c7c4f-1db3-4668-bebb-fd84b604aa7c",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:02:00.257",
      "raw": {
        "id": 405,
        "category": "clinical",
        "engine": "nextflow",
        "name": "enrichment_visualization",
        "display_name": "Enrichment Visualization",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Visualize enrichment results using enrichplot package functions. Use when creating publication-quality figures from clusterProfiler results. Covers dotplot, barplot, cnetplot, emapplot, gseaplot2, ridgeplot, and treeplot.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "139c7c4f-1db3-4668-bebb-fd84b604aa7c",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:00.257"
      }
    },
    {
      "source": "workflow_registry",
      "id": 444,
      "workflow_bundle_id": "686144c9-1a68-45ce-a612-f19364e57ddc",
      "category": "clinical",
      "engine": "nextflow",
      "name": "enzyme_selection",
      "display_name": "Enzyme Selection",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Select restriction enzymes by criteria using Biopython Bio.Restriction. Find enzymes that cut once, don't cut, produce specific overhangs, are commercially available, or have compatible ends for cloning. Use when selecting restriction enzymes for cloning or analysis.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "686144c9-1a68-45ce-a612-f19364e57ddc",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:11.005",
      "raw": {
        "id": 444,
        "category": "clinical",
        "engine": "nextflow",
        "name": "enzyme_selection",
        "display_name": "Enzyme Selection",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Select restriction enzymes by criteria using Biopython Bio.Restriction. Find enzymes that cut once, don't cut, produce specific overhangs, are commercially available, or have compatible ends for cloning. Use when selecting restriction enzymes for cloning or analysis.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "686144c9-1a68-45ce-a612-f19364e57ddc",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:11.005"
      }
    },
    {
      "source": "workflow_registry",
      "id": 358,
      "workflow_bundle_id": "e8fbcf49-4ee0-44dd-b66b-2ddd6402858b",
      "category": "clinical",
      "engine": "nextflow",
      "name": "epitope_prediction",
      "display_name": "Epitope Prediction",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Predict B-cell and T-cell epitopes using BepiPred, IEDB tools, and structure-based methods for vaccine and antibody design. Identify immunogenic regions in antigens. Use when designing vaccines, mapping antibody binding sites, or predicting immunogenic peptides.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "e8fbcf49-4ee0-44dd-b66b-2ddd6402858b",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:00:26.426",
      "raw": {
        "id": 358,
        "category": "clinical",
        "engine": "nextflow",
        "name": "epitope_prediction",
        "display_name": "Epitope Prediction",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Predict B-cell and T-cell epitopes using BepiPred, IEDB tools, and structure-based methods for vaccine and antibody design. Identify immunogenic regions in antigens. Use when designing vaccines, mapping antibody binding sites, or predicting immunogenic peptides.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "e8fbcf49-4ee0-44dd-b66b-2ddd6402858b",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:00:26.426"
      }
    },
    {
      "source": "workflow_registry",
      "id": 71,
      "workflow_bundle_id": "bdec58cf-4ecf-4740-9433-fa5652bd7c18",
      "category": "clinical",
      "engine": "nextflow",
      "name": "exome_clinical_v1",
      "display_name": "Clinical Exome Sequencing",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Clinical exome sequencing pipeline for rare disease diagnosis with ACMG variant classification, phenotype-driven prioritization, and clinical reporting.",
      "inputs_schema": "{\"input\": {\"type\": \"string\", \"description\": \"Samplesheet CSV\"}, \"genome\": {\"type\": \"string\", \"description\": \"Reference genome FASTA\"}, \"outdir\": {\"type\": \"string\", \"description\": \"Output directory\"}, \"target_regions\": {\"type\": \"string\", \"description\": \"Target regions BED file\"}}",
      "outputs": "[\"clinical_report.html\", \"acmg_classifications.csv\", \"coverage_report.json\", \"prioritized_variants.csv\"]",
      "container_image": null,
      "object_id": "bdec58cf-4ecf-4740-9433-fa5652bd7c18",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-23T00:16:20.859",
      "raw": {
        "id": 71,
        "category": "clinical",
        "engine": "nextflow",
        "name": "exome_clinical_v1",
        "display_name": "Clinical Exome Sequencing",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Clinical exome sequencing pipeline for rare disease diagnosis with ACMG variant classification, phenotype-driven prioritization, and clinical reporting.",
        "inputs_schema": "{\"input\": {\"type\": \"string\", \"description\": \"Samplesheet CSV\"}, \"genome\": {\"type\": \"string\", \"description\": \"Reference genome FASTA\"}, \"outdir\": {\"type\": \"string\", \"description\": \"Output directory\"}, \"target_regions\": {\"type\": \"string\", \"description\": \"Target regions BED file\"}}",
        "outputs": "[\"clinical_report.html\", \"acmg_classifications.csv\", \"coverage_report.json\", \"prioritized_variants.csv\"]",
        "container_image": null,
        "object_id": "bdec58cf-4ecf-4740-9433-fa5652bd7c18",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-05-23T00:16:20.859"
      }
    },
    {
      "source": "workflow_registry",
      "id": 439,
      "workflow_bundle_id": "68b5e70b-e933-4f61-9ed3-733c5aa52e40",
      "category": "clinical",
      "engine": "nextflow",
      "name": "fastp_workflow",
      "display_name": "Fastp Workflow",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "All-in-one read preprocessing with fastp including adapter trimming, quality filtering, deduplication, base correction, and HTML report generation. Use when preprocessing Illumina data and wanting a single fast tool instead of separate Cutadapt, Trimmomatic, and FastQC steps.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "68b5e70b-e933-4f61-9ed3-733c5aa52e40",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:01.976",
      "raw": {
        "id": 439,
        "category": "clinical",
        "engine": "nextflow",
        "name": "fastp_workflow",
        "display_name": "Fastp Workflow",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "All-in-one read preprocessing with fastp including adapter trimming, quality filtering, deduplication, base correction, and HTML report generation. Use when preprocessing Illumina data and wanting a single fast tool instead of separate Cutadapt, Trimmomatic, and FastQC steps.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "68b5e70b-e933-4f61-9ed3-733c5aa52e40",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:01.976"
      }
    },
    {
      "source": "workflow_registry",
      "id": 460,
      "workflow_bundle_id": "87fc396f-7f5f-411b-a413-061dab79b157",
      "category": "clinical",
      "engine": "nextflow",
      "name": "fastq_quality",
      "display_name": "Fastq Quality",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Work with FASTQ quality scores using Biopython. Use when analyzing read quality, filtering by quality, trimming low-quality bases, or generating quality reports.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "87fc396f-7f5f-411b-a413-061dab79b157",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:40.149",
      "raw": {
        "id": 460,
        "category": "clinical",
        "engine": "nextflow",
        "name": "fastq_quality",
        "display_name": "Fastq Quality",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Work with FASTQ quality scores using Biopython. Use when analyzing read quality, filtering by quality, trimming low-quality bases, or generating quality reports.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "87fc396f-7f5f-411b-a413-061dab79b157",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:40.149"
      }
    },
    {
      "source": "workflow_registry",
      "id": 461,
      "workflow_bundle_id": "d8526b88-0c20-4667-8d28-975de34af469",
      "category": "clinical",
      "engine": "nextflow",
      "name": "filter_sequences",
      "display_name": "Filter Sequences",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Filter and select sequences by criteria (length, ID, GC content, patterns) using Biopython. Use when subsetting sequences, removing unwanted records, or selecting by specific criteria.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d8526b88-0c20-4667-8d28-975de34af469",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:42.016",
      "raw": {
        "id": 461,
        "category": "clinical",
        "engine": "nextflow",
        "name": "filter_sequences",
        "display_name": "Filter Sequences",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Filter and select sequences by criteria (length, ID, GC content, patterns) using Biopython. Use when subsetting sequences, removing unwanted records, or selecting by specific criteria.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d8526b88-0c20-4667-8d28-975de34af469",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:42.016"
      }
    },
    {
      "source": "workflow_registry",
      "id": 503,
      "workflow_bundle_id": "068734f7-6b20-4b9a-8fb5-f28b2b5ae80d",
      "category": "clinical",
      "engine": "nextflow",
      "name": "filtering_best_practices",
      "display_name": "Filtering Best Practices",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Comprehensive variant filtering including GATK VQSR, hard filters, bcftools expressions, and quality metric interpretation for SNPs and indels. Use when filtering variants using GATK best practices.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "068734f7-6b20-4b9a-8fb5-f28b2b5ae80d",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:04:58.897",
      "raw": {
        "id": 503,
        "category": "clinical",
        "engine": "nextflow",
        "name": "filtering_best_practices",
        "display_name": "Filtering Best Practices",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Comprehensive variant filtering including GATK VQSR, hard filters, bcftools expressions, and quality metric interpretation for SNPs and indels. Use when filtering variants using GATK best practices.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "068734f7-6b20-4b9a-8fb5-f28b2b5ae80d",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:04:58.897"
      }
    },
    {
      "source": "workflow_registry",
      "id": 462,
      "workflow_bundle_id": "59b11b2d-ceee-471f-9611-8a517b613ca1",
      "category": "clinical",
      "engine": "nextflow",
      "name": "format_conversion",
      "display_name": "Format Conversion",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Convert between sequence file formats (FASTA, FASTQ, GenBank, EMBL) using Biopython Bio.SeqIO. Use when changing file formats or preparing data for different tools.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "59b11b2d-ceee-471f-9611-8a517b613ca1",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:43.826",
      "raw": {
        "id": 462,
        "category": "clinical",
        "engine": "nextflow",
        "name": "format_conversion",
        "display_name": "Format Conversion",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Convert between sequence file formats (FASTA, FASTQ, GenBank, EMBL) using Biopython Bio.SeqIO. Use when changing file formats or preparing data for different tools.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "59b11b2d-ceee-471f-9611-8a517b613ca1",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:43.826"
      }
    },
    {
      "source": "workflow_registry",
      "id": 364,
      "workflow_bundle_id": "ebcde9a8-dcaa-43cd-a1aa-e94cf830605a",
      "category": "clinical",
      "engine": "nextflow",
      "name": "fragment_analysis",
      "display_name": "Fragment Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Analyzes cfDNA fragment size distributions and fragmentomics features using FinaleToolkit or Griffin. Extracts nucleosome positioning patterns, fragment ratios, and DELFI-style fragmentation profiles for cancer detection. Use when leveraging fragment patterns for tumor detection or tissue-of-origin ",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "ebcde9a8-dcaa-43cd-a1aa-e94cf830605a",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:00:39.263",
      "raw": {
        "id": 364,
        "category": "clinical",
        "engine": "nextflow",
        "name": "fragment_analysis",
        "display_name": "Fragment Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Analyzes cfDNA fragment size distributions and fragmentomics features using FinaleToolkit or Griffin. Extracts nucleosome positioning patterns, fragment ratios, and DELFI-style fragmentation profiles for cancer detection. Use when leveraging fragment patterns for tumor detection or tissue-of-origin ",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "ebcde9a8-dcaa-43cd-a1aa-e94cf830605a",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:00:39.263"
      }
    },
    {
      "source": "workflow_registry",
      "id": 445,
      "workflow_bundle_id": "1a8be85c-f035-4684-9947-ffd4628729aa",
      "category": "clinical",
      "engine": "nextflow",
      "name": "fragment_analysis_v2",
      "display_name": "Fragment Analysis v2",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Analyze restriction digest fragments using Biopython Bio.Restriction. Predict fragment sizes, get fragment sequences, simulate gel electrophoresis patterns, and perform double digests. Use when analyzing restriction digest fragment patterns.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "1a8be85c-f035-4684-9947-ffd4628729aa",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:12.813",
      "raw": {
        "id": 445,
        "category": "clinical",
        "engine": "nextflow",
        "name": "fragment_analysis_v2",
        "display_name": "Fragment Analysis v2",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Analyze restriction digest fragments using Biopython Bio.Restriction. Predict fragment sizes, get fragment sequences, simulate gel electrophoresis patterns, and perform double digests. Use when analyzing restriction digest fragment patterns.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "1a8be85c-f035-4684-9947-ffd4628729aa",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:12.813"
      }
    },
    {
      "source": "workflow_registry",
      "id": 99,
      "workflow_bundle_id": "e6cd115e-45bc-48ed-8262-c02f76e52c4f",
      "category": "clinical",
      "engine": "nextflow",
      "name": "fusion_detection",
      "display_name": "Fusion Detection",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "STAR-Fusion, Arriba, FusionCatcher parallel gene fusion detection with merged output",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": "docker.io/man4ish/omnibioai-fusion:1.0",
      "object_id": "e6cd115e-45bc-48ed-8262-c02f76e52c4f",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-05T23:05:13.291",
      "raw": {
        "id": 99,
        "category": "clinical",
        "engine": "nextflow",
        "name": "fusion_detection",
        "display_name": "Fusion Detection",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "STAR-Fusion, Arriba, FusionCatcher parallel gene fusion detection with merged output",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-fusion:1.0",
        "object_id": "e6cd115e-45bc-48ed-8262-c02f76e52c4f",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-05T23:05:13.291"
      }
    },
    {
      "source": "workflow_registry",
      "id": 147,
      "workflow_bundle_id": "c8d5a9c7-629c-4e87-863c-151be223218f",
      "category": "clinical",
      "engine": "nextflow",
      "name": "gatk_cnv_v2",
      "display_name": "GATK Somatic CNV Calling v2",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "GATK somatic CNV calling with read count collection, denoising, segmentation, and copy ratio calling",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "c8d5a9c7-629c-4e87-863c-151be223218f",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:48:18.136",
      "raw": {
        "id": 147,
        "category": "clinical",
        "engine": "nextflow",
        "name": "gatk_cnv_v2",
        "display_name": "GATK Somatic CNV Calling v2",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "GATK somatic CNV calling with read count collection, denoising, segmentation, and copy ratio calling",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c8d5a9c7-629c-4e87-863c-151be223218f",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:48:18.136"
      }
    },
    {
      "source": "workflow_registry",
      "id": 144,
      "workflow_bundle_id": "303f9bad-1846-4f0c-8b5f-af9f9e33afff",
      "category": "clinical",
      "engine": "nextflow",
      "name": "gatk_germline_v2",
      "display_name": "GATK Germline Variant Calling v2",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "GATK HaplotypeCaller germline variant calling with MarkDuplicates, GVCF genotyping, and variant filtration",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "303f9bad-1846-4f0c-8b5f-af9f9e33afff",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:48:12.761",
      "raw": {
        "id": 144,
        "category": "clinical",
        "engine": "nextflow",
        "name": "gatk_germline_v2",
        "display_name": "GATK Germline Variant Calling v2",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "GATK HaplotypeCaller germline variant calling with MarkDuplicates, GVCF genotyping, and variant filtration",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "303f9bad-1846-4f0c-8b5f-af9f9e33afff",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:48:12.761"
      }
    },
    {
      "source": "workflow_registry",
      "id": 504,
      "workflow_bundle_id": "255acea5-b910-4ab9-80e1-77c9003c1eea",
      "category": "clinical",
      "engine": "nextflow",
      "name": "gatk_variant_calling",
      "display_name": "Gatk Variant Calling",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Variant calling with GATK HaplotypeCaller following best practices. Covers germline SNP/indel calling, GVCF workflow for cohorts, joint genotyping, and variant quality score recalibration (VQSR). Use when calling variants with GATK HaplotypeCaller.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "255acea5-b910-4ab9-80e1-77c9003c1eea",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:05:00.746",
      "raw": {
        "id": 504,
        "category": "clinical",
        "engine": "nextflow",
        "name": "gatk_variant_calling",
        "display_name": "Gatk Variant Calling",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Variant calling with GATK HaplotypeCaller following best practices. Covers germline SNP/indel calling, GVCF workflow for cohorts, joint genotyping, and variant quality score recalibration (VQSR). Use when calling variants with GATK HaplotypeCaller.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "255acea5-b910-4ab9-80e1-77c9003c1eea",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:05:00.746"
      }
    },
    {
      "source": "workflow_registry",
      "id": 406,
      "workflow_bundle_id": "cb94ce06-afda-4fda-98c0-91fac00bca7f",
      "category": "clinical",
      "engine": "nextflow",
      "name": "go_enrichment",
      "display_name": "GO Enrichment",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Gene Ontology over-representation analysis using clusterProfiler enrichGO. Use when identifying biological functions enriched in a gene list from differential expression or other analyses. Supports all three ontologies (BP, MF, CC), multiple ID types, and customizable statistical thresholds.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "cb94ce06-afda-4fda-98c0-91fac00bca7f",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:02:02.052",
      "raw": {
        "id": 406,
        "category": "clinical",
        "engine": "nextflow",
        "name": "go_enrichment",
        "display_name": "GO Enrichment",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Gene Ontology over-representation analysis using clusterProfiler enrichGO. Use when identifying biological functions enriched in a gene list from differential expression or other analyses. Supports all three ontologies (BP, MF, CC), multiple ID types, and customizable statistical thresholds.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "cb94ce06-afda-4fda-98c0-91fac00bca7f",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:02.052"
      }
    },
    {
      "source": "workflow_registry",
      "id": 407,
      "workflow_bundle_id": "9b7e651a-6857-4617-bbfa-d8235f096ec2",
      "category": "clinical",
      "engine": "nextflow",
      "name": "gsea",
      "display_name": "GSEA",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Gene Set Enrichment Analysis using clusterProfiler gseGO and gseKEGG. Use when analyzing ranked gene lists to find coordinated expression changes in gene sets without arbitrary significance cutoffs. Detects subtle but coordinated expression changes.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "9b7e651a-6857-4617-bbfa-d8235f096ec2",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:02:03.850",
      "raw": {
        "id": 407,
        "category": "clinical",
        "engine": "nextflow",
        "name": "gsea",
        "display_name": "GSEA",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Gene Set Enrichment Analysis using clusterProfiler gseGO and gseKEGG. Use when analyzing ranked gene lists to find coordinated expression changes in gene sets without arbitrary significance cutoffs. Detects subtle but coordinated expression changes.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "9b7e651a-6857-4617-bbfa-d8235f096ec2",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:03.850"
      }
    },
    {
      "source": "workflow_registry",
      "id": 623,
      "workflow_bundle_id": "216986e6-3763-45f1-9908-b36bb9ebf412",
      "category": "clinical",
      "engine": "nextflow",
      "name": "gwas_prs_analysis",
      "display_name": "GWAS and Polygenic Risk Score",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Run GWAS and compute polygenic risk scores using PLINK2 and PRSice-2.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "216986e6-3763-45f1-9908-b36bb9ebf412",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:34:59.709",
      "raw": {
        "id": 623,
        "category": "clinical",
        "engine": "nextflow",
        "name": "gwas_prs_analysis",
        "display_name": "GWAS and Polygenic Risk Score",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Run GWAS and compute polygenic risk scores using PLINK2 and PRSice-2.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "216986e6-3763-45f1-9908-b36bb9ebf412",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:34:59.709"
      }
    },
    {
      "source": "workflow_registry",
      "id": 435,
      "workflow_bundle_id": "91c2f2c9-56c3-4e09-ab7f-e53eb101ae0c",
      "category": "clinical",
      "engine": "nextflow",
      "name": "hisat2_alignment",
      "display_name": "Hisat2 Alignment",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Align RNA-seq reads with HISAT2, a memory-efficient splice-aware aligner. Use when STAR's memory requirements are too high or for general RNA-seq alignment.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "91c2f2c9-56c3-4e09-ab7f-e53eb101ae0c",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:02:54.555",
      "raw": {
        "id": 435,
        "category": "clinical",
        "engine": "nextflow",
        "name": "hisat2_alignment",
        "display_name": "Hisat2 Alignment",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Align RNA-seq reads with HISAT2, a memory-efficient splice-aware aligner. Use when STAR's memory requirements are too high or for general RNA-seq alignment.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "91c2f2c9-56c3-4e09-ab7f-e53eb101ae0c",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:54.555"
      }
    },
    {
      "source": "workflow_registry",
      "id": 61,
      "workflow_bundle_id": "612facbe-8a86-479c-be49-61c419116872",
      "category": "clinical",
      "engine": "nextflow",
      "name": "hla_typing_v1",
      "display_name": "HLA Typing",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "HLA allele typing pipeline from WGS/WES/RNA-seq data with peptide-MHC binding prediction and immunopeptidome analysis.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "612facbe-8a86-479c-be49-61c419116872",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-22T21:41:35.529",
      "raw": {
        "id": 61,
        "category": "clinical",
        "engine": "nextflow",
        "name": "hla_typing_v1",
        "display_name": "HLA Typing",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "HLA allele typing pipeline from WGS/WES/RNA-seq data with peptide-MHC binding prediction and immunopeptidome analysis.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "612facbe-8a86-479c-be49-61c419116872",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-05-22T21:41:35.529"
      }
    },
    {
      "source": "workflow_registry",
      "id": 359,
      "workflow_bundle_id": "5fbaa78a-fbff-4dfd-847d-b598fc764be5",
      "category": "clinical",
      "engine": "nextflow",
      "name": "immunogenicity_scoring",
      "display_name": "Immunogenicity Scoring",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Score and prioritize neoantigens and epitopes for immunogenicity using multi-factor models combining MHC binding, processing, expression, and sequence features. Rank candidates for vaccine design. Use when prioritizing epitopes for vaccine development or identifying the most immunogenic neoantigens.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "5fbaa78a-fbff-4dfd-847d-b598fc764be5",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:00:28.238",
      "raw": {
        "id": 359,
        "category": "clinical",
        "engine": "nextflow",
        "name": "immunogenicity_scoring",
        "display_name": "Immunogenicity Scoring",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Score and prioritize neoantigens and epitopes for immunogenicity using multi-factor models combining MHC binding, processing, expression, and sequence features. Rank candidates for vaccine design. Use when prioritizing epitopes for vaccine development or identifying the most immunogenic neoantigens.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "5fbaa78a-fbff-4dfd-847d-b598fc764be5",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:00:28.238"
      }
    },
    {
      "source": "workflow_registry",
      "id": 354,
      "workflow_bundle_id": "2f7705dc-5eeb-4fee-a58d-c3d0d0aeabed",
      "category": "clinical",
      "engine": "nextflow",
      "name": "interactive_annotation",
      "display_name": "Interactive Annotation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Interactive cell annotation and image QC for IMC/MIBI using napari, napari-imc, Mantis Viewer, and cytomapper, covering the pixels-to-cell-table bridge, overlaying masks to catch segmentation/spillover artifacts, inter-annotator variability as the accuracy ceiling, contrast-as-threshold, and buildin",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "2f7705dc-5eeb-4fee-a58d-c3d0d0aeabed",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:00:19.021",
      "raw": {
        "id": 354,
        "category": "clinical",
        "engine": "nextflow",
        "name": "interactive_annotation",
        "display_name": "Interactive Annotation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Interactive cell annotation and image QC for IMC/MIBI using napari, napari-imc, Mantis Viewer, and cytomapper, covering the pixels-to-cell-table bridge, overlaying masks to catch segmentation/spillover artifacts, inter-annotator variability as the accuracy ceiling, contrast-as-threshold, and buildin",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "2f7705dc-5eeb-4fee-a58d-c3d0d0aeabed",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:00:19.021"
      }
    },
    {
      "source": "workflow_registry",
      "id": 505,
      "workflow_bundle_id": "ec3be753-4aae-4015-9acb-429366dbd244",
      "category": "clinical",
      "engine": "nextflow",
      "name": "joint_calling",
      "display_name": "Joint Calling",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Joint genotype calling across multiple samples using GATK CombineGVCFs and GenotypeGVCFs. Essential for cohort studies, population genetics, and leveraging VQSR. Use when performing joint genotyping across multiple samples.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "ec3be753-4aae-4015-9acb-429366dbd244",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:05:02.546",
      "raw": {
        "id": 505,
        "category": "clinical",
        "engine": "nextflow",
        "name": "joint_calling",
        "display_name": "Joint Calling",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Joint genotype calling across multiple samples using GATK CombineGVCFs and GenotypeGVCFs. Essential for cohort studies, population genetics, and leveraging VQSR. Use when performing joint genotyping across multiple samples.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "ec3be753-4aae-4015-9acb-429366dbd244",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:05:02.546"
      }
    },
    {
      "source": "workflow_registry",
      "id": 408,
      "workflow_bundle_id": "7d30a338-6504-4a05-9968-8b9f18c31838",
      "category": "clinical",
      "engine": "nextflow",
      "name": "kegg_pathways",
      "display_name": "KEGG Pathways",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "KEGG pathway and module enrichment analysis using clusterProfiler enrichKEGG and enrichMKEGG. Use when identifying metabolic and signaling pathways over-represented in a gene list. Supports 4000+ organisms via KEGG online database.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "7d30a338-6504-4a05-9968-8b9f18c31838",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:02:05.661",
      "raw": {
        "id": 408,
        "category": "clinical",
        "engine": "nextflow",
        "name": "kegg_pathways",
        "display_name": "KEGG Pathways",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "KEGG pathway and module enrichment analysis using clusterProfiler enrichKEGG and enrichMKEGG. Use when identifying metabolic and signaling pathways over-represented in a gene list. Supports 4000+ organisms via KEGG online database.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "7d30a338-6504-4a05-9968-8b9f18c31838",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:05.661"
      }
    },
    {
      "source": "workflow_registry",
      "id": 638,
      "workflow_bundle_id": "a4984b4c-9c00-44b8-9c3b-4357ab5afa3c",
      "category": "clinical",
      "engine": "nextflow",
      "name": "ldsc_genetic_correlation",
      "display_name": "LDSC Genetic Correlation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Estimate genetic correlation between traits using bivariate LD Score Regression.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "a4984b4c-9c00-44b8-9c3b-4357ab5afa3c",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:44:49.389",
      "raw": {
        "id": 638,
        "category": "clinical",
        "engine": "nextflow",
        "name": "ldsc_genetic_correlation",
        "display_name": "LDSC Genetic Correlation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Estimate genetic correlation between traits using bivariate LD Score Regression.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "a4984b4c-9c00-44b8-9c3b-4357ab5afa3c",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:44:49.389"
      }
    },
    {
      "source": "workflow_registry",
      "id": 637,
      "workflow_bundle_id": "cfe7c5f6-fbb9-47af-bf15-34016082b8cd",
      "category": "clinical",
      "engine": "nextflow",
      "name": "ldsc_heritability",
      "display_name": "LDSC Heritability Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Partition SNP heritability by functional annotation using LD Score Regression (LDSC).",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "cfe7c5f6-fbb9-47af-bf15-34016082b8cd",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:44:47.547",
      "raw": {
        "id": 637,
        "category": "clinical",
        "engine": "nextflow",
        "name": "ldsc_heritability",
        "display_name": "LDSC Heritability Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Partition SNP heritability by functional annotation using LD Score Regression (LDSC).",
        "inputs_schema": null,
        "outputs": "[]",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Performs logistic regression for clinical trial outcomes (binary, ordinal, multinomial) with marginal-vs-conditional estimand reporting per FDA 2023 covariate adjustment guidance, g-computation/standardisation for marginal effects, modified Poisson for RR, Brant test for proportional odds, Firth pen",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "bdf4011a-5635-448e-9d96-6e3f8f1d4875",
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        "display_name": "Logistic Regression",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Performs logistic regression for clinical trial outcomes (binary, ordinal, multinomial) with marginal-vs-conditional estimand reporting per FDA 2023 covariate adjustment guidance, g-computation/standardisation for marginal effects, modified Poisson for RR, Brant test for proportional odds, Firth pen",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "bdf4011a-5635-448e-9d96-6e3f8f1d4875",
        "enabled": 1,
        "created_by": "manish",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Tracks ctDNA dynamics over time for treatment response monitoring using serial liquid biopsy samples. Analyzes tumor fraction trends, mutation clearance kinetics, and defines molecular response criteria. Use when monitoring patients during therapy or detecting molecular relapse before clinical progr",
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      "container_image": null,
      "object_id": "04c99185-d405-4352-b563-f3f6e01b7ca4",
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        "description": "Tracks ctDNA dynamics over time for treatment response monitoring using serial liquid biopsy samples. Analyzes tumor fraction trends, mutation clearance kinetics, and defines molecular response criteria. Use when monitoring patients during therapy or detecting molecular relapse before clinical progr",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "04c99185-d405-4352-b563-f3f6e01b7ca4",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Analyzes cfDNA methylation patterns for cancer detection using cfMeDIP-seq or bisulfite sequencing with MethylDackel. Identifies cancer-specific methylation signatures and performs tissue-of-origin deconvolution. Use when using methylation biomarkers for early cancer detection or minimal residual di",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "b81c47c5-34e1-4eba-b248-8dcc68268335",
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Analyzes cfDNA methylation patterns for cancer detection using cfMeDIP-seq or bisulfite sequencing with MethylDackel. Identifies cancer-specific methylation signatures and performs tissue-of-origin deconvolution. Use when using methylation biomarkers for early cancer detection or minimal residual di",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "b81c47c5-34e1-4eba-b248-8dcc68268335",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Predict peptide-MHC class I and II binding affinity using MHCflurry and NetMHCpan neural network models. Identify potential T-cell epitopes from protein sequences. Use when predicting MHC binding for vaccine design or neoantigen identification.",
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      "outputs": "[]",
      "container_image": null,
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Predict peptide-MHC class I and II binding affinity using MHCflurry and NetMHCpan neural network models. Identify potential T-cell epitopes from protein sequences. Use when predicting MHC binding for vaccine design or neoantigen identification.",
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        "outputs": "[]",
        "container_image": null,
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Implements missing-data sensitivity analyses for confirmatory clinical trials including MMRM under MAR (with Kenward-Roger correction), reference-based multiple imputation (J2R, CR, CIR, LMCF per Carpenter-Roger 2013), Permutt delta-adjustment / tipping-point analysis, pattern-mixture identifying re",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "1000730c-73bc-4c88-a703-4fc2f54eaf2a",
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        "engine": "nextflow",
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Implements missing-data sensitivity analyses for confirmatory clinical trials including MMRM under MAR (with Kenward-Roger correction), reference-based multiple imputation (J2R, CR, CIR, LMCF per Carpenter-Roger 2013), Permutt delta-adjustment / tipping-point analysis, pattern-mixture identifying re",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "1000730c-73bc-4c88-a703-4fc2f54eaf2a",
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        "created_by": "manish",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Find patterns, motifs, and subsequences in biological sequences using Biopython. Use when searching for transcription factor binding sites, regulatory elements, or any sequence pattern. For restriction enzyme analysis, use the restriction-analysis skill.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "7c0fcda6-047f-4a42-9cf2-2c4ec373024a",
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        "category": "clinical",
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        "name": "motif_search",
        "display_name": "Motif Search",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Find patterns, motifs, and subsequences in biological sequences using Biopython. Use when searching for transcription factor binding sites, regulatory elements, or any sequence pattern. For restriction enzyme analysis, use the restriction-analysis skill.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "7c0fcda6-047f-4a42-9cf2-2c4ec373024a",
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        "created_by": "manish",
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      "id": 97,
      "workflow_bundle_id": "a53e2896-a3ab-489c-a6cf-c06095a25bdf",
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      "engine": "nextflow",
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      "display_name": "MSI / TMB Profiling",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "MSIsensor2 microsatellite instability scoring and TMB calculation from somatic VCF",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": "docker.io/man4ish/omnibioai-clinical:1.0",
      "object_id": "a53e2896-a3ab-489c-a6cf-c06095a25bdf",
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      "created_by": "manish",
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      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "msi_tmb_profiling",
        "display_name": "MSI / TMB Profiling",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "MSIsensor2 microsatellite instability scoring and TMB calculation from somatic VCF",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-clinical:1.0",
        "object_id": "a53e2896-a3ab-489c-a6cf-c06095a25bdf",
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        "created_by": "manish",
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    {
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      "id": 218,
      "workflow_bundle_id": "7fce0dbd-b034-4b02-a4d2-91f343812098",
      "category": "clinical",
      "engine": "nextflow",
      "name": "multiplicity_graphical",
      "display_name": "Multiplicity Graphical",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Implements multiplicity control for confirmatory clinical trials using graphical procedures (Bretz-Maurer-Hommel), gatekeeping (parallel, serial, mixed), Hochberg/Hommel/Holm with PRDS, and the closed-testing principle (Marcus-Peritz-Gabriel; Goeman 2021 admissibility). Covers FDA Multiple Endpoints",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "7fce0dbd-b034-4b02-a4d2-91f343812098",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:56:09.609",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "multiplicity_graphical",
        "display_name": "Multiplicity Graphical",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Implements multiplicity control for confirmatory clinical trials using graphical procedures (Bretz-Maurer-Hommel), gatekeeping (parallel, serial, mixed), Hochberg/Hommel/Holm with PRDS, and the closed-testing principle (Marcus-Peritz-Gabriel; Goeman 2021 admissibility). Covers FDA Multiple Endpoints",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "7fce0dbd-b034-4b02-a4d2-91f343812098",
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        "created_at": "2026-06-08T01:56:09.609"
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    {
      "source": "workflow_registry",
      "id": 98,
      "workflow_bundle_id": "b3cc6751-b1aa-4bb3-9d4d-a77bf561cbf8",
      "category": "clinical",
      "engine": "nextflow",
      "name": "neoantigen_prediction",
      "display_name": "Neoantigen Prediction",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "pVACseq + MHCflurry HLA typing and MHC-I/II binding affinity neoantigen ranking",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": "docker.io/man4ish/omnibioai-clinical:1.0",
      "object_id": "b3cc6751-b1aa-4bb3-9d4d-a77bf561cbf8",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-05T23:05:11.567",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "neoantigen_prediction",
        "display_name": "Neoantigen Prediction",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "pVACseq + MHCflurry HLA typing and MHC-I/II binding affinity neoantigen ranking",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-clinical:1.0",
        "object_id": "b3cc6751-b1aa-4bb3-9d4d-a77bf561cbf8",
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        "created_by": "manish",
        "created_at": "2026-06-05T23:05:11.567"
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      "id": 37,
      "workflow_bundle_id": "42bc5b99-309d-4851-bad0-d96943150078",
      "category": "clinical",
      "engine": "nextflow",
      "name": "omnibioai_gatk_nextflow_v1",
      "display_name": "GATK4 Germline Variant Calling (Nextflow)",
      "version": "0.1.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "GATK4 Best Practices germline variant calling pipeline: BWA-MEM alignment, MarkDuplicates, BQSR, HaplotypeCaller (gVCF), and GenotypeGVCFs (single-sample mode).",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "42bc5b99-309d-4851-bad0-d96943150078",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-04-04T06:17:01.427",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "omnibioai_gatk_nextflow_v1",
        "display_name": "GATK4 Germline Variant Calling (Nextflow)",
        "version": "0.1.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "GATK4 Best Practices germline variant calling pipeline: BWA-MEM alignment, MarkDuplicates, BQSR, HaplotypeCaller (gVCF), and GenotypeGVCFs (single-sample mode).",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "42bc5b99-309d-4851-bad0-d96943150078",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-04-04T06:17:01.427"
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    {
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      "id": 36,
      "workflow_bundle_id": "e9ce2fae-50b1-46f0-a922-af8c65ebb2f3",
      "category": "clinical",
      "engine": "nextflow",
      "name": "omnibioai_wes_nextflow_v1",
      "display_name": "Whole Exome Sequencing (Nextflow)",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "WES analysis pipeline using Nextflow",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "e9ce2fae-50b1-46f0-a922-af8c65ebb2f3",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-04-04T06:14:58.393",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "omnibioai_wes_nextflow_v1",
        "display_name": "Whole Exome Sequencing (Nextflow)",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "WES analysis pipeline using Nextflow",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "e9ce2fae-50b1-46f0-a922-af8c65ebb2f3",
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        "created_by": "manish",
        "created_at": "2026-04-04T06:14:58.393"
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    {
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      "id": 463,
      "workflow_bundle_id": "de13f8d3-cfa7-46a8-b2c4-51edeb3d7db9",
      "category": "clinical",
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      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Handle paired-end FASTQ files (R1/R2) using Biopython. Use when working with Illumina paired reads, synchronizing pairs, interleaving/deinterleaving, or filtering paired data.",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "de13f8d3-cfa7-46a8-b2c4-51edeb3d7db9",
      "enabled": 1,
      "created_by": "manish",
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        "engine": "nextflow",
        "name": "paired_end_fastq",
        "display_name": "Paired End Fastq",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Handle paired-end FASTQ files (R1/R2) using Biopython. Use when working with Illumina paired reads, synchronizing pairs, interleaving/deinterleaving, or filtering paired data.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "de13f8d3-cfa7-46a8-b2c4-51edeb3d7db9",
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        "created_by": "manish",
        "created_at": "2026-06-08T02:03:45.629"
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      "id": 54,
      "workflow_bundle_id": "8343e1ac-34ec-4bd9-b9c0-731233efb62c",
      "category": "clinical",
      "engine": "nextflow",
      "name": "pharmacogenomics_v1",
      "display_name": "Pharmacogenomics Analysis Pipeline",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Analyze pharmacogenomic variants from patient VCF to predict drug metabolism phenotypes (CYP2D6, CYP2C19, CYP2C9, CYP3A5, NAT2) and generate personalized drug recommendations.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "8343e1ac-34ec-4bd9-b9c0-731233efb62c",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-22T07:26:08.113",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "pharmacogenomics_v1",
        "display_name": "Pharmacogenomics Analysis Pipeline",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Analyze pharmacogenomic variants from patient VCF to predict drug metabolism phenotypes (CYP2D6, CYP2C19, CYP2C9, CYP3A5, NAT2) and generate personalized drug recommendations.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "8343e1ac-34ec-4bd9-b9c0-731233efb62c",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-05-22T07:26:08.113"
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    {
      "source": "workflow_registry",
      "id": 355,
      "workflow_bundle_id": "ff798301-c515-499f-a35d-b5c488c5e04b",
      "category": "clinical",
      "engine": "nextflow",
      "name": "phenotyping",
      "display_name": "Phenotyping",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Assign cell types from marker expression in IMC/MIBI data using clustering (PhenoGraph/FlowSOM/Leiden/Pixie), marker-based probabilistic classifiers (Astir), or image-context CNNs (CellSighter), covering the double-positive segmentation artifact, lineage-vs-state markers, the two spillover types, an",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "ff798301-c515-499f-a35d-b5c488c5e04b",
      "enabled": 1,
      "created_by": "manish",
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      "raw": {
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        "engine": "nextflow",
        "name": "phenotyping",
        "display_name": "Phenotyping",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Assign cell types from marker expression in IMC/MIBI data using clustering (PhenoGraph/FlowSOM/Leiden/Pixie), marker-based probabilistic classifiers (Astir), or image-context CNNs (CellSighter), covering the double-positive segmentation artifact, lineage-vs-state markers, the two spillover types, an",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "ff798301-c515-499f-a35d-b5c488c5e04b",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:00:20.926"
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    },
    {
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      "id": 219,
      "workflow_bundle_id": "d2c7d3d8-e2d6-4b50-8ff9-9fccab00666e",
      "category": "clinical",
      "engine": "nextflow",
      "name": "power_and_sample_size",
      "display_name": "Power And Sample Size",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Computes sample size and power for clinical trials including continuous, binary, and time-to-event endpoints; superiority, non-inferiority, and equivalence designs; FDA 2016 non-inferiority margin selection with M1/M2 framework; Schoenfeld 1981 and Lakatos 1988 for survival; Schuirmann TOST and 80-1",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d2c7d3d8-e2d6-4b50-8ff9-9fccab00666e",
      "enabled": 1,
      "created_by": "manish",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "power_and_sample_size",
        "display_name": "Power And Sample Size",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Computes sample size and power for clinical trials including continuous, binary, and time-to-event endpoints; superiority, non-inferiority, and equivalence designs; FDA 2016 non-inferiority margin selection with M1/M2 framework; Schoenfeld 1981 and Lakatos 1988 for survival; Schuirmann TOST and 80-1",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d2c7d3d8-e2d6-4b50-8ff9-9fccab00666e",
        "enabled": 1,
        "created_by": "manish",
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    {
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      "id": 421,
      "workflow_bundle_id": "e4b32d9b-2503-4e64-85e1-acca32f6d0c5",
      "category": "clinical",
      "engine": "nextflow",
      "name": "primer_basics",
      "display_name": "Primer Basics",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Design PCR primers for a target sequence using primer3-py. Specify target regions, product size, melting temperature, and other constraints. Returns ranked primer pairs with quality metrics. Use when designing standard PCR primers.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "e4b32d9b-2503-4e64-85e1-acca32f6d0c5",
      "enabled": 1,
      "created_by": "manish",
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      "raw": {
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        "engine": "nextflow",
        "name": "primer_basics",
        "display_name": "Primer Basics",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Design PCR primers for a target sequence using primer3-py. Specify target regions, product size, melting temperature, and other constraints. Returns ranked primer pairs with quality metrics. Use when designing standard PCR primers.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "e4b32d9b-2503-4e64-85e1-acca32f6d0c5",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:29.009"
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    {
      "source": "workflow_registry",
      "id": 422,
      "workflow_bundle_id": "ae987a50-6b89-4ef2-8c97-42632718fde1",
      "category": "clinical",
      "engine": "nextflow",
      "name": "primer_validation",
      "display_name": "Primer Validation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Validate PCR primers for specificity, dimers, hairpins, and secondary structures using primer3-py thermodynamic calculations. Check self-complementarity, heterodimer formation, and 3' stability. Use when validating primer specificity and properties.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "ae987a50-6b89-4ef2-8c97-42632718fde1",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:02:30.800",
      "raw": {
        "id": 422,
        "category": "clinical",
        "engine": "nextflow",
        "name": "primer_validation",
        "display_name": "Primer Validation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Validate PCR primers for specificity, dimers, hairpins, and secondary structures using primer3-py thermodynamic calculations. Check self-complementarity, heterodimer formation, and 3' stability. Use when validating primer specificity and properties.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "ae987a50-6b89-4ef2-8c97-42632718fde1",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:30.800"
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    },
    {
      "source": "workflow_registry",
      "id": 529,
      "workflow_bundle_id": "7dfc7394-4fc5-40f7-a5a8-817a5c0d279a",
      "category": "clinical",
      "engine": "nextflow",
      "name": "pydicom_imaging",
      "display_name": "Pydicom Imaging",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Read, write, and manipulate DICOM medical imaging files (CT, MRI, X-ray) using pydicom.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "7dfc7394-4fc5-40f7-a5a8-817a5c0d279a",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:09:33.007",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "pydicom_imaging",
        "display_name": "Pydicom Imaging",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Read, write, and manipulate DICOM medical imaging files (CT, MRI, X-ray) using pydicom.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "7dfc7394-4fc5-40f7-a5a8-817a5c0d279a",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:09:33.007"
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    {
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      "id": 423,
      "workflow_bundle_id": "30be8bfc-8157-43a0-8b80-ec32dd744667",
      "category": "clinical",
      "engine": "nextflow",
      "name": "qpcr_primers",
      "display_name": "Qpcr Primers",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Design qPCR primers and TaqMan/molecular beacon probes using primer3-py. Configure probe Tm, primer-probe spacing, and hydrolysis probe constraints for real-time PCR assays. Use when designing qPCR primers and probes.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "30be8bfc-8157-43a0-8b80-ec32dd744667",
      "enabled": 1,
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      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "qpcr_primers",
        "display_name": "Qpcr Primers",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Design qPCR primers and TaqMan/molecular beacon probes using primer3-py. Configure probe Tm, primer-probe spacing, and hydrolysis probe constraints for real-time PCR assays. Use when designing qPCR primers and probes.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "30be8bfc-8157-43a0-8b80-ec32dd744667",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:32.609"
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    {
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      "id": 440,
      "workflow_bundle_id": "31845117-baa4-4335-92fc-339cac35e200",
      "category": "clinical",
      "engine": "nextflow",
      "name": "quality_filtering",
      "display_name": "Quality Filtering",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Filter reads by quality scores, length, and N content using Trimmomatic and fastp. Apply sliding window trimming, remove low-quality bases from read ends, and discard reads below thresholds. Use when reads have poor quality tails or require minimum quality for downstream analysis.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "31845117-baa4-4335-92fc-339cac35e200",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:03.772",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "quality_filtering",
        "display_name": "Quality Filtering",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Filter reads by quality scores, length, and N content using Trimmomatic and fastp. Apply sliding window trimming, remove low-quality bases from read ends, and discard reads below thresholds. Use when reads have poor quality tails or require minimum quality for downstream analysis.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "31845117-baa4-4335-92fc-339cac35e200",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:03.772"
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    {
      "source": "workflow_registry",
      "id": 356,
      "workflow_bundle_id": "b8573ee3-b5a5-437b-b4c8-26576e5b27ad",
      "category": "clinical",
      "engine": "nextflow",
      "name": "quality_metrics",
      "display_name": "Quality Metrics",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Quality control for IMC/MIBI data across pixel, channel, image, slide, and batch levels, covering Poisson-count SNR (cell-level Gaussian-mixture and empty-channel comparison), spillover-matrix QC (the three physical sources), drift and the missing EQ-bead analog, acquisition artifacts, and sample-of",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "b8573ee3-b5a5-437b-b4c8-26576e5b27ad",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:00:22.751",
      "raw": {
        "id": 356,
        "category": "clinical",
        "engine": "nextflow",
        "name": "quality_metrics",
        "display_name": "Quality Metrics",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Quality control for IMC/MIBI data across pixel, channel, image, slide, and batch levels, covering Poisson-count SNR (cell-level Gaussian-mixture and empty-channel comparison), spillover-matrix QC (the three physical sources), drift and the missing EQ-bead analog, acquisition artifacts, and sample-of",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "b8573ee3-b5a5-437b-b4c8-26576e5b27ad",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:00:22.751"
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    {
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      "id": 441,
      "workflow_bundle_id": "5ae43af7-195f-4c31-8a83-7c7a54d91e0c",
      "category": "clinical",
      "engine": "nextflow",
      "name": "quality_reports",
      "display_name": "Quality Reports",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Generate and interpret quality reports from FASTQ files using FastQC and MultiQC. Assess per-base quality, adapter content, GC bias, duplication levels, and overrepresented sequences. Use when performing initial QC on raw sequencing data or validating preprocessing results.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "5ae43af7-195f-4c31-8a83-7c7a54d91e0c",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:05.592",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "quality_reports",
        "display_name": "Quality Reports",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Generate and interpret quality reports from FASTQ files using FastQC and MultiQC. Assess per-base quality, adapter content, GC bias, duplication levels, and overrepresented sequences. Use when performing initial QC on raw sequencing data or validating preprocessing results.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "5ae43af7-195f-4c31-8a83-7c7a54d91e0c",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:05.592"
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    {
      "source": "workflow_registry",
      "id": 409,
      "workflow_bundle_id": "ba65941f-30ab-4d11-a0b9-674e21d035d2",
      "category": "clinical",
      "engine": "nextflow",
      "name": "reactome_pathways",
      "display_name": "Reactome Pathways",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Reactome pathway enrichment using ReactomePA package. Use when analyzing gene lists against Reactome's curated peer-reviewed pathway database. Performs over-representation analysis and GSEA with visualization and pathway hierarchy exploration.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "ba65941f-30ab-4d11-a0b9-674e21d035d2",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:02:07.456",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "reactome_pathways",
        "display_name": "Reactome Pathways",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Reactome pathway enrichment using ReactomePA package. Use when analyzing gene lists against Reactome's curated peer-reviewed pathway database. Performs over-representation analysis and GSEA with visualization and pathway hierarchy exploration.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "ba65941f-30ab-4d11-a0b9-674e21d035d2",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:07.456"
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    {
      "source": "workflow_registry",
      "id": 464,
      "workflow_bundle_id": "d2b13386-0bee-4772-bb83-a5ebf486bcce",
      "category": "clinical",
      "engine": "nextflow",
      "name": "read_sequences",
      "display_name": "Read Sequences",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Read biological sequence files (FASTA, FASTQ, GenBank, EMBL, ABI, SFF) using Biopython Bio.SeqIO. Use when parsing sequence files, iterating multi-sequence files, random access to large files, or high-performance parsing.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d2b13386-0bee-4772-bb83-a5ebf486bcce",
      "enabled": 1,
      "created_by": "manish",
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      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "read_sequences",
        "display_name": "Read Sequences",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Read biological sequence files (FASTA, FASTQ, GenBank, EMBL, ABI, SFF) using Biopython Bio.SeqIO. Use when parsing sequence files, iterating multi-sequence files, random access to large files, or high-performance parsing.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d2b13386-0bee-4772-bb83-a5ebf486bcce",
        "enabled": 1,
        "created_by": "manish",
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      "id": 446,
      "workflow_bundle_id": "a73646dc-36bd-499b-9b2a-df9d8217fad3",
      "category": "clinical",
      "engine": "nextflow",
      "name": "restriction_mapping",
      "display_name": "Restriction Mapping",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Create restriction maps showing enzyme cut positions on DNA sequences using Biopython Bio.Restriction. Visualize cut sites, calculate distances between sites, and generate text or graphical maps. Use when creating or analyzing restriction maps.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "a73646dc-36bd-499b-9b2a-df9d8217fad3",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:14.609",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "restriction_mapping",
        "display_name": "Restriction Mapping",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Create restriction maps showing enzyme cut positions on DNA sequences using Biopython Bio.Restriction. Visualize cut sites, calculate distances between sites, and generate text or graphical maps. Use when creating or analyzing restriction maps.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "a73646dc-36bd-499b-9b2a-df9d8217fad3",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:14.609"
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    {
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      "id": 447,
      "workflow_bundle_id": "764dff10-23f7-4db5-a465-98f4d2c8dc01",
      "category": "clinical",
      "engine": "nextflow",
      "name": "restriction_sites",
      "display_name": "Restriction Sites",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Find restriction enzyme cut sites in DNA sequences using Biopython Bio.Restriction. Search with single enzymes, batches of enzymes, or commercially available enzyme sets. Returns cut positions for linear or circular DNA. Use when finding restriction enzyme cut sites in sequences.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "764dff10-23f7-4db5-a465-98f4d2c8dc01",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:16.422",
      "raw": {
        "id": 447,
        "category": "clinical",
        "engine": "nextflow",
        "name": "restriction_sites",
        "display_name": "Restriction Sites",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Find restriction enzyme cut sites in DNA sequences using Biopython Bio.Restriction. Search with single enzymes, batches of enzymes, or commercially available enzyme sets. Returns cut positions for linear or circular DNA. Use when finding restriction enzyme cut sites in sequences.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "764dff10-23f7-4db5-a465-98f4d2c8dc01",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:16.422"
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    {
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      "id": 469,
      "workflow_bundle_id": "d8edd7be-e1e1-4d68-9537-f3e7159685f0",
      "category": "clinical",
      "engine": "nextflow",
      "name": "reverse_complement",
      "display_name": "Reverse Complement",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Generate reverse complements and complements of DNA/RNA sequences using Biopython. Use when working with opposite strands, primer design, or converting between template and coding strands.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d8edd7be-e1e1-4d68-9537-f3e7159685f0",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:56.355",
      "raw": {
        "id": 469,
        "category": "clinical",
        "engine": "nextflow",
        "name": "reverse_complement",
        "display_name": "Reverse Complement",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Generate reverse complements and complements of DNA/RNA sequences using Biopython. Use when working with opposite strands, primer design, or converting between template and coding strands.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d8edd7be-e1e1-4d68-9537-f3e7159685f0",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "RNA-seq specific quality control including rRNA contamination detection, strandedness verification, gene body coverage, and transcript integrity metrics. Use when validating RNA-seq libraries before differential expression analysis.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "58153224-de62-4d42-b378-8f8db7fc9be7",
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      "created_at": "2026-06-08T02:03:07.387",
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        "engine": "nextflow",
        "name": "rnaseq_qc",
        "display_name": "RNASEQ QC",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "RNA-seq specific quality control including rRNA contamination detection, strandedness verification, gene body coverage, and transcript integrity metrics. Use when validating RNA-seq libraries before differential expression analysis.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "58153224-de62-4d42-b378-8f8db7fc9be7",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:07.387"
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      "workflow_bundle_id": "ac5563ab-6e1e-4e58-b480-21384853a9c7",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Create and manipulate Seq, MutableSeq, and SeqRecord objects using Biopython. Use when creating sequences from strings, modifying sequence data in-place, or building annotated sequence records.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "ac5563ab-6e1e-4e58-b480-21384853a9c7",
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        "engine": "nextflow",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Create and manipulate Seq, MutableSeq, and SeqRecord objects using Biopython. Use when creating sequences from strings, modifying sequence data in-place, or building annotated sequence records.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "ac5563ab-6e1e-4e58-b480-21384853a9c7",
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        "created_by": "manish",
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    {
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      "id": 471,
      "workflow_bundle_id": "036e10a7-483a-4a99-8c48-a9b714d21bf4",
      "category": "clinical",
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      "display_name": "Sequence Properties",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Calculate sequence properties like GC content, molecular weight, isoelectric point, and GC skew using Biopython. Use when analyzing sequence composition, computing physical properties, or comparing sequences.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "036e10a7-483a-4a99-8c48-a9b714d21bf4",
      "enabled": 1,
      "created_by": "manish",
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      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
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        "display_name": "Sequence Properties",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Calculate sequence properties like GC content, molecular weight, isoelectric point, and GC skew using Biopython. Use when analyzing sequence composition, computing physical properties, or comparing sequences.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "036e10a7-483a-4a99-8c48-a9b714d21bf4",
        "enabled": 1,
        "created_by": "manish",
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    {
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      "id": 472,
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      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "Sequence Slicing",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Slice, extract, and concatenate biological sequences using Biopython. Use when extracting subsequences, joining sequences, or manipulating sequence regions by position.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "3b4730f0-0b30-4806-9760-48531bf8cebb",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:04:01.816",
      "raw": {
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        "engine": "nextflow",
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        "display_name": "Sequence Slicing",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Slice, extract, and concatenate biological sequences using Biopython. Use when extracting subsequences, joining sequences, or manipulating sequence regions by position.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "3b4730f0-0b30-4806-9760-48531bf8cebb",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:04:01.816"
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    {
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      "id": 465,
      "workflow_bundle_id": "6eb4046a-af5a-4812-a8bd-0c3737f12478",
      "category": "clinical",
      "engine": "nextflow",
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      "display_name": "Sequence Statistics",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Calculate sequence statistics (N50, length distribution, GC content, summary reports) using Biopython. Use when analyzing sequence datasets, generating QC reports, or comparing assemblies.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "6eb4046a-af5a-4812-a8bd-0c3737f12478",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:49.206",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "sequence_statistics",
        "display_name": "Sequence Statistics",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Calculate sequence statistics (N50, length distribution, GC content, summary reports) using Biopython. Use when analyzing sequence datasets, generating QC reports, or comparing assemblies.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "6eb4046a-af5a-4812-a8bd-0c3737f12478",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:49.206"
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    {
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      "id": 530,
      "workflow_bundle_id": "c81e42c1-0cf0-46c9-85d9-5bb8f9d52c8d",
      "category": "clinical",
      "engine": "nextflow",
      "name": "simpleitk_registration",
      "display_name": "Simpleitk Registration",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Medical image registration, segmentation, and filtering for MRI/CT volumes using SimpleITK.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "c81e42c1-0cf0-46c9-85d9-5bb8f9d52c8d",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:09:34.907",
      "raw": {
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        "name": "simpleitk_registration",
        "display_name": "Simpleitk Registration",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Medical image registration, segmentation, and filtering for MRI/CT volumes using SimpleITK.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c81e42c1-0cf0-46c9-85d9-5bb8f9d52c8d",
        "enabled": 1,
        "created_by": "manish",
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    {
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      "workflow_bundle_id": "f20b25ac-8417-45be-b2de-b45c2e7637d3",
      "category": "clinical",
      "engine": "nextflow",
      "name": "somatic_variant_calling",
      "display_name": "Somatic Variant Calling",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "GATK Mutect2 tumor-normal somatic SNV/indel calling with FilterMutectCalls and Funcotator annotation",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": "docker.io/man4ish/omnibioai-clinical:1.0",
      "object_id": "f20b25ac-8417-45be-b2de-b45c2e7637d3",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-05T23:05:06.321",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "somatic_variant_calling",
        "display_name": "Somatic Variant Calling",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "GATK Mutect2 tumor-normal somatic SNV/indel calling with FilterMutectCalls and Funcotator annotation",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-clinical:1.0",
        "object_id": "f20b25ac-8417-45be-b2de-b45c2e7637d3",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-05T23:05:06.321"
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    },
    {
      "source": "workflow_registry",
      "id": 436,
      "workflow_bundle_id": "9fdd5528-f499-4cd8-ab49-024a22c98e4e",
      "category": "clinical",
      "engine": "nextflow",
      "name": "star_alignment",
      "display_name": "Star Alignment",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Align RNA-seq reads with STAR (Spliced Transcripts Alignment to a Reference). Supports two-pass mode for novel splice junction discovery. Use when aligning RNA-seq data requiring splice-aware alignment.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "9fdd5528-f499-4cd8-ab49-024a22c98e4e",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:02:56.418",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "star_alignment",
        "display_name": "Star Alignment",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Align RNA-seq reads with STAR (Spliced Transcripts Alignment to a Reference). Supports two-pass mode for novel splice junction discovery. Use when aligning RNA-seq data requiring splice-aware alignment.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "9fdd5528-f499-4cd8-ab49-024a22c98e4e",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:56.418"
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    {
      "source": "workflow_registry",
      "id": 506,
      "workflow_bundle_id": "e5df3dd5-d82f-4af0-a4f2-2b39d044f144",
      "category": "clinical",
      "engine": "nextflow",
      "name": "structural_variant_calling",
      "display_name": "Structural Variant Calling",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Call structural variants (SVs) from sequencing data using Manta, Delly, GRIDSS, and LUMPY. Detects deletions, insertions, inversions, duplications, and translocations too large for standard SNV callers. Use when detecting structural variants from short-read or long-read data and building consensus c",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "e5df3dd5-d82f-4af0-a4f2-2b39d044f144",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:05:04.395",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "structural_variant_calling",
        "display_name": "Structural Variant Calling",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Call structural variants (SVs) from sequencing data using Manta, Delly, GRIDSS, and LUMPY. Detects deletions, insertions, inversions, duplications, and translocations too large for standard SNV callers. Use when detecting structural variants from short-read or long-read data and building consensus c",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "e5df3dd5-d82f-4af0-a4f2-2b39d044f144",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:05:04.395"
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    {
      "source": "workflow_registry",
      "id": 220,
      "workflow_bundle_id": "22df3a0e-3fba-4e20-91df-2a09b8a102f5",
      "category": "clinical",
      "engine": "nextflow",
      "name": "subgroup_analysis",
      "display_name": "Subgroup Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Performs subgroup and heterogeneous treatment effect (HTE) analyses for clinical trials. Covers Mantel-Haenszel pooling, Breslow-Day, interaction tests in regression, RERI for additive interaction, modern data-adaptive HTE methods (STEPP, SIDES, causal forests, X/R-learners), Bayesian shrinkage (Dix",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "22df3a0e-3fba-4e20-91df-2a09b8a102f5",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:56:13.301",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "subgroup_analysis",
        "display_name": "Subgroup Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Performs subgroup and heterogeneous treatment effect (HTE) analyses for clinical trials. Covers Mantel-Haenszel pooling, Breslow-Day, interaction tests in regression, RERI for additive interaction, modern data-adaptive HTE methods (STEPP, SIDES, causal forests, X/R-learners), Bayesian shrinkage (Dix",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "22df3a0e-3fba-4e20-91df-2a09b8a102f5",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:56:13.301"
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    {
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      "id": 221,
      "workflow_bundle_id": "bd456340-f2a4-404d-b565-b3aa57b5ecb9",
      "category": "clinical",
      "engine": "nextflow",
      "name": "survival_analysis",
      "display_name": "Survival Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Performs time-to-event analysis for clinical trials including Cox proportional hazards regression with PH diagnostics, restricted mean survival time (RMST) under non-PH, competing risks via Fine-Gray vs cause-specific Cox, weighted log-rank and MaxCombo for non-proportional hazards, recurrent events",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "bd456340-f2a4-404d-b565-b3aa57b5ecb9",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:56:15.127",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "survival_analysis",
        "display_name": "Survival Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Performs time-to-event analysis for clinical trials including Cox proportional hazards regression with PH diagnostics, restricted mean survival time (RMST) under non-PH, competing risks via Fine-Gray vs cause-specific Cox, weighted log-rank and MaxCombo for non-proportional hazards, recurrent events",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "bd456340-f2a4-404d-b565-b3aa57b5ecb9",
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        "created_by": "manish",
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    {
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      "name": "susie_finemapping",
      "display_name": "SuSiE Fine-mapping",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Fine-map causal variants in GWAS loci using SuSiE sum of single effects regression.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "cd523022-f940-4b80-9059-2f6615e0286f",
      "enabled": 1,
      "created_by": "manish",
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      "raw": {
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        "display_name": "SuSiE Fine-mapping",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Fine-map causal variants in GWAS loci using SuSiE sum of single effects regression.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "cd523022-f940-4b80-9059-2f6615e0286f",
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      "display_name": "Structural Variant Calling v2",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Structural variant calling with Manta and SURVIVOR merge",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "ea85ec35-89a3-4d5d-9893-b72f65e6251e",
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        "engine": "nextflow",
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        "display_name": "Structural Variant Calling v2",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Structural variant calling with Manta and SURVIVOR merge",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "ea85ec35-89a3-4d5d-9893-b72f65e6251e",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Structural variant detection pipeline using Delly. Processes BAM files to identify deletions, insertions, duplications, inversions, and translocations.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "0c66e0d8-0fab-4ab5-ab0d-e16200c5ad0f",
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      "created_by": "manish",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Structural variant detection pipeline using Delly. Processes BAM files to identify deletions, insertions, duplications, inversions, and translocations.",
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        "description": "Transcribe DNA to RNA and translate to protein using Biopython. Use when converting between DNA, RNA, and protein sequences, finding ORFs, or using alternative codon tables.",
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      "configs": "[\"config/input.json\"]",
      "description": "Prepares statistical reports for clinical trials following CONSORT 2025, SPIRIT 2025, ICH E9(R1) estimands, and FDA 2023 covariate adjustment guidance. Covers Table 1 generation, analysis populations (ITT/FAS/PP/Safety), the 5 ICH E9(R1) intercurrent-event strategies, MMRM under MAR (mmrm), referenc",
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        "description": "Prepares statistical reports for clinical trials following CONSORT 2025, SPIRIT 2025, ICH E9(R1) estimands, and FDA 2023 covariate adjustment guidance. Covers Table 1 generation, analysis populations (ITT/FAS/PP/Safety), the 5 ICH E9(R1) intercurrent-event strategies, MMRM under MAR (mmrm), referenc",
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      "description": "Estimates circulating tumor DNA fraction from shallow whole-genome sequencing using ichorCNA. Detects copy number alterations via HMM segmentation and calculates ctDNA percentage. Requires 0.1-1x sWGS coverage. Use when quantifying tumor burden from liquid biopsy or monitoring treatment response.",
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        "display_name": "Tumor Fraction Estimation",
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        "description": "Estimates circulating tumor DNA fraction from shallow whole-genome sequencing using ichorCNA. Detects copy number alterations via HMM segmentation and calculates ctDNA percentage. Requires 0.1-1x sWGS coverage. Use when quantifying tumor burden from liquid biopsy or monitoring treatment response.",
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      "configs": "[\"config/input.json\"]",
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        "configs": "[\"config/input.json\"]",
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      "configs": "[\"config/input.json\"]",
      "description": "Extract, process, and deduplicate reads using Unique Molecular Identifiers (UMIs) with umi_tools. Use when library prep includes UMIs and accurate molecule counting is needed, such as in single-cell RNA-seq, low-input RNA-seq, or targeted sequencing to distinguish PCR from biological duplicates.",
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        "description": "Extract, process, and deduplicate reads using Unique Molecular Identifiers (UMIs) with umi_tools. Use when library prep includes UMIs and accurate molecule counting is needed, such as in single-cell RNA-seq, low-input RNA-seq, or targeted sequencing to distinguish PCR from biological duplicates.",
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      "configs": "[\"config/input.json\"]",
      "description": "Variant annotation with Ensembl VEP and PASS variant filtering with bcftools",
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        "engine": "nextflow",
        "name": "variant_annotation",
        "display_name": "Variant Annotation with VEP",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Variant annotation with Ensembl VEP and PASS variant filtering with bcftools",
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        "container_image": null,
        "object_id": "d0efe7ad-483a-479a-9c99-e3044d16b1cc",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Call SNPs and indels from aligned reads using bcftools mpileup and call. Use when detecting variants from BAM files or generating VCF from alignments.",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "2f0bd3de-325b-4177-982e-9fdf9da286df",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "variant_calling",
        "display_name": "Variant Calling",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Call SNPs and indels from aligned reads using bcftools mpileup and call. Use when detecting variants from BAM files or generating VCF from alignments.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "2f0bd3de-325b-4177-982e-9fdf9da286df",
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        "created_by": "manish",
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      "workflow_bundle_id": "e76ec201-53c2-41ba-b533-f3e7962cc450",
      "category": "clinical",
      "engine": "nextflow",
      "name": "variant_ml_scoring_v1",
      "display_name": "Variant ML Annotation & Scoring Pipeline",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "ML pipeline for scoring genomic variants using functional + sequence-based features",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "e76ec201-53c2-41ba-b533-f3e7962cc450",
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      "created_by": "manish",
      "created_at": "2026-04-17T03:56:33.890",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "variant_ml_scoring_v1",
        "display_name": "Variant ML Annotation & Scoring Pipeline",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "ML pipeline for scoring genomic variants using functional + sequence-based features",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "e76ec201-53c2-41ba-b533-f3e7962cc450",
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        "created_by": "manish",
        "created_at": "2026-04-17T03:56:33.890"
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      "category": "clinical",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Normalize indel representation, decompose MNPs, and split multiallelic variants using bcftools norm. Use when comparing variants from different callers, preparing VCF for database annotation, or merging VCFs from multiple sources.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "4d79a43c-b651-4727-8482-62c238f45110",
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        "category": "clinical",
        "engine": "nextflow",
        "name": "variant_normalization",
        "display_name": "Variant Normalization",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Normalize indel representation, decompose MNPs, and split multiallelic variants using bcftools norm. Use when comparing variants from different callers, preparing VCF for database annotation, or merging VCFs from multiple sources.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "4d79a43c-b651-4727-8482-62c238f45110",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:05:07.984"
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    {
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      "workflow_bundle_id": "32b7b1c7-f348-4722-b2ec-fa8d8fdc02f8",
      "category": "clinical",
      "engine": "nextflow",
      "name": "variant_surveillance",
      "display_name": "Genomic Variant Surveillance",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Track pathogen variant emergence and spread using Nextclade and phylogenetic analysis.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "32b7b1c7-f348-4722-b2ec-fa8d8fdc02f8",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:32:56.022",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "variant_surveillance",
        "display_name": "Genomic Variant Surveillance",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Track pathogen variant emergence and spread using Nextclade and phylogenetic analysis.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "32b7b1c7-f348-4722-b2ec-fa8d8fdc02f8",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:32:56.022"
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    {
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      "workflow_bundle_id": "ce1afac7-a42b-41f2-a2a4-744a8d79e989",
      "category": "clinical",
      "engine": "nextflow",
      "name": "vcf_basics",
      "display_name": "VCF Basics",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "View, query, and understand VCF/BCF variant files using bcftools and cyvcf2. Use when inspecting variants, extracting specific fields, or understanding VCF format structure.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "ce1afac7-a42b-41f2-a2a4-744a8d79e989",
      "enabled": 1,
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      "created_at": "2026-06-08T02:05:09.848",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "vcf_basics",
        "display_name": "VCF Basics",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "View, query, and understand VCF/BCF variant files using bcftools and cyvcf2. Use when inspecting variants, extracting specific fields, or understanding VCF format structure.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "ce1afac7-a42b-41f2-a2a4-744a8d79e989",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:05:09.848"
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    {
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      "id": 510,
      "workflow_bundle_id": "54136949-b2dd-4934-ab74-04a25b934fc5",
      "category": "clinical",
      "engine": "nextflow",
      "name": "vcf_manipulation",
      "display_name": "VCF Manipulation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Merge, concatenate, sort, intersect, and subset VCF files using bcftools. Use when combining variant files, comparing call sets, or restructuring VCF data.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "54136949-b2dd-4934-ab74-04a25b934fc5",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:05:11.723",
      "raw": {
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        "category": "clinical",
        "engine": "nextflow",
        "name": "vcf_manipulation",
        "display_name": "VCF Manipulation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Merge, concatenate, sort, intersect, and subset VCF files using bcftools. Use when combining variant files, comparing call sets, or restructuring VCF data.",
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        "outputs": "[]",
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      "object_id": "8098a2c8-7188-445a-9b88-ec93509f9a71",
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        "container_image": null,
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      "configs": "[\"config/input.json\"]",
      "description": "ViFi and VirusBreakend HPV/EBV/HBV viral integration site detection",
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        "description": "ViFi and VirusBreakend HPV/EBV/HBV viral integration site detection",
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        "outputs": "[]",
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      "container_image": null,
      "object_id": "f9ae7b40-67a2-49a2-83ae-40dad0c3c451",
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        "outputs": "[]",
        "container_image": null,
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      "description": "Write biological sequences to files (FASTA, FASTQ, GenBank, EMBL) using Biopython Bio.SeqIO. Use when saving sequences, creating new sequence files, or outputting modified records.",
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      "container_image": null,
      "object_id": "712a0951-35ee-4c5d-b216-50a68af8549c",
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        "description": "Write biological sequences to files (FASTA, FASTQ, GenBank, EMBL) using Biopython Bio.SeqIO. Use when saving sequences, creating new sequence files, or outputting modified records.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "712a0951-35ee-4c5d-b216-50a68af8549c",
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        "configs": "[\"config/inputs.json\"]",
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      "configs": "[\"config/inputs.json\"]",
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      "outputs": "[]",
      "container_image": "ghcr.io/man4ish/omnibioai-mageck-crispr:1.0.0",
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        "entrypoint": "workflow/main.nf",
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        "outputs": "[]",
        "container_image": "ghcr.io/man4ish/omnibioai-mageck-crispr:1.0.0",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
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      "outputs": "[]",
      "container_image": null,
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        "outputs": "[]",
        "container_image": null,
        "object_id": "70c93b29-bd7e-470a-9211-73a0ba1dbe04",
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      "configs": "[\"config/input.json\"]",
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      "container_image": null,
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        "outputs": "[]",
        "container_image": null,
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        "container_image": null,
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      "entrypoint": "workflow/main.nf",
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      "container_image": null,
      "object_id": "7d6512bf-f3cb-4f97-8f0c-9a0ff0b72a86",
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        "entrypoint": "workflow/main.nf",
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        "description": "Annotate CLIP-seq peaks or crosslink sites to RNA features (5'UTR, CDS, 3'UTR, intron, splice junction, snoRNA, tRNA, ncRNA, repeat elements) with ChIPseeker, RCAS, RBP-Maps (Yeo splicing regulatory maps), and bedtools, applying feature-priority hierarchies, transcript-context resolution, and metage",
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        "container_image": null,
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      "container_image": null,
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        "configs": "[\"config/input.json\"]",
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        "container_image": null,
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      "description": "Call protein-RNA binding sites from CLIP-seq BAM with CLIPper, PureCLIP, Skipper, Piranha, omniCLIP, CTK, CLAM, or Paraclu. Use when choosing between coverage-based, HMM-based, beta-binomial window-based, and crosslink-site-based peak callers; applying ENCODE eCLIP thresholds (log2 IP/SMInput >= 3, ",
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      "outputs": "[]",
      "container_image": null,
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        "container_image": null,
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      "container_image": null,
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      "container_image": null,
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        "container_image": null,
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      "container_image": null,
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        "description": "Identify differentially bound regions across CLIP-seq conditions (knockdown vs control, treatment vs vehicle, disease vs healthy) using DEWSeq (sliding-window DESeq2), Flipper (Skipper-downstream), ASpeak, edgeR, or limma-voom. Use when computing condition-level changes in RBP binding intensity, cho",
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      "configs": "[\"config/input.json\"]",
      "description": "Per-CpG differential methylation testing from bisulfite sequencing count data or beta-value matrices. Covers beta and M-value computation, coverage filtering, statistical tests (Welch t-test, Mann-Whitney, limma, DSS beta-binomial), multiple testing correction, and effect size calculation. Use when ",
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        "description": "Per-CpG differential methylation testing from bisulfite sequencing count data or beta-value matrices. Covers beta and M-value computation, coverage filtering, statistical tests (Welch t-test, Mann-Whitney, limma, DSS beta-binomial), multiple testing correction, and effect size calculation. Use when ",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
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        "outputs": "[]",
        "container_image": null,
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      "description": "BWA alignment, MACS2 open chromatin peak calling and annotation for FAIRE-seq",
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    {
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        "description": "Query JASPAR database for transcription factor binding site profiles (PWMs/PFMs) for motif analysis.",
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        "outputs": "[]",
        "container_image": null,
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      "entrypoint": "workflow/main.nf",
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      "description": "Map N6-methyladenosine (m6A) RNA modifications at single-nucleotide resolution using miCLIP (Linder 2015), miCLIP2 + m6Aboost machine learning (Kortel 2021), GLORI (Liu 2023, antibody-free chemical conversion), DART-seq (Meyer 2019, APOBEC1-YTH fusion), m6Anet (nanopore direct RNA), or MeRIP-seq wit",
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      "outputs": "[]",
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        "entrypoint": "workflow/main.nf",
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        "description": "Map N6-methyladenosine (m6A) RNA modifications at single-nucleotide resolution using miCLIP (Linder 2015), miCLIP2 + m6Aboost machine learning (Kortel 2021), GLORI (Liu 2023, antibody-free chemical conversion), DART-seq (Meyer 2019, APOBEC1-YTH fusion), m6Anet (nanopore direct RNA), or MeRIP-seq wit",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "70c75b13-f4f4-4187-8497-e2db2bddfcc0",
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    {
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      "id": 44,
      "workflow_bundle_id": "ce461787-d9c7-4219-8ca8-d3a95730cdc8",
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      "engine": "nextflow",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Bisulfite sequencing methylation analysis using Bismark + QC + MultiQC",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "ce461787-d9c7-4219-8ca8-d3a95730cdc8",
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      "created_by": "manish",
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        "engine": "nextflow",
        "name": "methylation_bismark_pipeline",
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Bisulfite sequencing methylation analysis using Bismark + QC + MultiQC",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "ce461787-d9c7-4219-8ca8-d3a95730cdc8",
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      "workflow_bundle_id": "4d2e7cc6-c58f-4022-a820-5c9c5bcbdcdd",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Extract methylation calls from Bismark BAM files using bismark_methylation_extractor. Generates per-cytosine reports for CpG, CHG, and CHH contexts. Use when extracting methylation levels from aligned bisulfite sequencing data for downstream analysis.",
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      "outputs": "[]",
      "container_image": null,
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Extract methylation calls from Bismark BAM files using bismark_methylation_extractor. Generates per-cytosine reports for CpG, CHG, and CHH contexts. Use when extracting methylation levels from aligned bisulfite sequencing data for downstream analysis.",
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        "outputs": "[]",
        "container_image": null,
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "DNA methylation analysis with methylKit in R. Import Bismark coverage files, filter by coverage, normalize samples, and perform statistical comparisons. Use when analyzing single-base methylation patterns, comparing samples, or preparing data for DMR detection.",
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      "container_image": null,
      "object_id": "d31133f3-2689-4398-a52e-6c6fdfdb393b",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "DNA methylation analysis with methylKit in R. Import Bismark coverage files, filter by coverage, normalize samples, and perform statistical comparisons. Use when analyzing single-base methylation patterns, comparing samples, or preparing data for DMR detection.",
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        "outputs": "[]",
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      "entrypoint": "workflow/main.nf",
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      "description": "BWA alignment, MACS3 peak calling with spike-in normalization for MINT-ChIP",
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        "description": "BWA alignment, MACS3 peak calling with spike-in normalization for MINT-ChIP",
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      "container_image": null,
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        "description": "Discovers de novo motifs and tests known motif enrichment in ChIP-seq, ATAC-seq, or other peak sequences using HOMER, MEME-ChIP (STREME, CentriMo, TOMTOM, FIMO), monaLisa, and AME. Handles background selection (GC-matched, dinucleotide-shuffled, Markov order-2, peak-flanks), motif databases (JASPAR ",
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        "container_image": null,
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        "description": "Nextflow wrapper workflow for nf-core/chipseq, nf-core/cutandrun, and nf-core/cutandtag with standardized outputs for OmniBioAI epigenomics analysis.",
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      "id": 107,
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Bismark dual GpC/CpG methylation calling for nucleosome occupancy and methylome sequencing",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Bismark dual GpC/CpG methylation calling for nucleosome occupancy and methylome sequencing",
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        "engine": "nextflow",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Annotates ChIP-seq peaks to genomic features, nearest genes, ENCODE candidate cis-regulatory elements (cCREs), and regulatory domains. Uses ChIPseeker (R), HOMER annotatePeaks.pl (CLI), pyranges (Python), GREAT/rGREAT (regulatory domain gene-set enrichment), ChIP-Enrich (locus-length-adjusted), ENCO",
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        "container_image": null,
        "object_id": "2948ae0d-78f5-4a80-8744-ea41e11a368e",
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      "category": "epigenomics",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Calls ChIP-seq peaks with MACS3, MACS2, HOMER, or SPP across narrow (TF) and broad (histone) modes. Handles input control matching, fragment-size modeling vs --nomodel, effective genome size, ENCODE-style IDR vs naive overlap, hyper-ChIPable artifacts, and aligner-specific shifts. Use when calling p",
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      "container_image": null,
      "object_id": "781c1c77-00be-412b-8bf9-565396acc8ec",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Calls ChIP-seq peaks with MACS3, MACS2, HOMER, or SPP across narrow (TF) and broad (histone) modes. Handles input control matching, fragment-size modeling vs --nomodel, effective genome size, ENCODE-style IDR vs naive overlap, hyper-ChIPable artifacts, and aligner-specific shifts. Use when calling p",
        "inputs_schema": null,
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        "outputs": "[]",
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      "description": "Remove mapping bias and identify allele-specific ChIP-seq binding using WASP.",
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      "container_image": null,
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        "configs": "[\"config/input.json\"]",
        "description": "Remove mapping bias and identify allele-specific ChIP-seq binding using WASP.",
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        "outputs": "[]",
        "container_image": null,
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      "container_image": null,
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        "configs": "[\"config/input.json\"]",
        "description": "Reconstruct ancestral states at internal phylogenetic nodes for sequences (PAML codeml, IQ-TREE --ancestral, GRASP, FastML), discrete traits (corHMM hidden-rate Markov, ape::ace, phytools::make.simmap stochastic mapping, BayesTraits), and continuous traits (phytools::fastAnc, geiger Brownian/OU, RPA",
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        "container_image": null,
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Genome-wide association studies (GWAS) with PLINK. Perform case-control and quantitative trait association testing using logistic/linear regression with covariates, generate Manhattan and QQ plots for result visualization. Use when running GWAS or association tests.",
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        "configs": "[\"config/input.json\"]",
        "description": "Genome-wide association studies (GWAS) with PLINK. Perform case-control and quantitative trait association testing using logistic/linear regression with covariates, generate Manhattan and QQ plots for result visualization. Use when running GWAS or association tests.",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Designs cytosine (CBE, C-to-T) and adenine (ABE, A-to-G) base-editor guides by positioning the target base at the activity-peak of the editing window (protospacer positions ~5-7, PAM-distal numbering), minimizing bystander edits for product purity, reading dinucleotide context (APOBEC1 TC favored / ",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Designs cytosine (CBE, C-to-T) and adenine (ABE, A-to-G) base-editor guides by positioning the target base at the activity-peak of the editing window (protospacer positions ~5-7, PAM-distal numbering), minimizing bystander edits for product purity, reading dinucleotide context (APOBEC1 TC favored / ",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Handles BED-format genomic intervals (BED3 through BED12, narrowPeak/broadPeak) and the coordinate-system substrate the whole interval category rests on, with bedtools (CLI) and pybedtools/pyranges/pandas (Python). Covers the 0-based half-open vs 1-based-closed convention boundary and the start-1/en",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Handles BED-format genomic intervals (BED3 through BED12, narrowPeak/broadPeak) and the coordinate-system substrate the whole interval category rests on, with bedtools (CLI) and pybedtools/pyranges/pandas (Python). Covers the 0-based half-open vs 1-based-closed convention boundary and the start-1/en",
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        "outputs": "[]",
        "container_image": null,
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      "entrypoint": "workflow/main.nf",
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      "container_image": null,
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Generates, normalizes, and converts bedGraph signal tracks (4-column chrom/start/end/value, 0-based half-open) with bedtools genomecov, deepTools bamCoverage/bamCompare/bigwigCompare, bedtools unionbedg, and UCSC bedGraphToBigWig. Covers why a raw coverage bedGraph is not comparable across samples u",
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        "container_image": null,
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        "configs": "[\"config/input.json\"]",
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "af538c1d-9952-45d8-af0e-358abbdc81e8",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
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      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
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        "created_by": "manish",
        "created_at": "2026-06-08T01:57:26.576"
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      "id": 261,
      "workflow_bundle_id": "633b6e16-e4b6-4fe8-a53a-9bf6480915f3",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "crispr_screens_batch_correction",
      "display_name": "CRISPR Screens Batch Correction",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Batch effect correction for CRISPR screens covering ComBat empirical-Bayes, RUV, SVA, control-sgRNA normalization, and the model-based alternative of including batch as a covariate in MAGeCK MLE or Chronos. Covers screen-specific batch sources (passage cohort, library lot, infection day, sequencing ",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "633b6e16-e4b6-4fe8-a53a-9bf6480915f3",
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      "created_by": "manish",
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        "engine": "nextflow",
        "name": "crispr_screens_batch_correction",
        "display_name": "CRISPR Screens Batch Correction",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Batch effect correction for CRISPR screens covering ComBat empirical-Bayes, RUV, SVA, control-sgRNA normalization, and the model-based alternative of including batch as a covariate in MAGeCK MLE or Chronos. Covers screen-specific batch sources (passage cohort, library lot, infection day, sequencing ",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
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        "created_by": "manish",
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      "workflow_bundle_id": "41039774-a005-4703-bde0-c035ea473dfa",
      "category": "funcgen",
      "engine": "nextflow",
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      "display_name": "CRISPR Screens Combinatorial Screens",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Designs and analyzes combinatorial CRISPR screens covering paired-Cas9 (Big Papi, Najm 2018), enhanced AsCas12a multiplex (enCas12a, DeWeirdt 2021), in4mer 4-guide-array Cas12a (Esmaeili Anvar N et al 2024 Nat Commun 15:3577) and the Inzolia paralog-pair library, paralog-buffering detection (Dede 20",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
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      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:30.270",
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        "display_name": "CRISPR Screens Combinatorial Screens",
        "version": "1.0.0",
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        "configs": "[\"config/input.json\"]",
        "description": "Designs and analyzes combinatorial CRISPR screens covering paired-Cas9 (Big Papi, Najm 2018), enhanced AsCas12a multiplex (enCas12a, DeWeirdt 2021), in4mer 4-guide-array Cas12a (Esmaeili Anvar N et al 2024 Nat Commun 15:3577) and the Inzolia paralog-pair library, paralog-buffering detection (Dede 20",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "41039774-a005-4703-bde0-c035ea473dfa",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:57:30.270"
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      "id": 263,
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      "category": "funcgen",
      "engine": "nextflow",
      "name": "crispr_screens_copy_number_correction",
      "display_name": "CRISPR Screens Copy Number Correction",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Corrects the gene-independent copy-number artifact in CRISPR-Cas9 screens (Aguirre 2016 / Munoz 2016 Cancer Discov) where amplified loci appear essential from DNA-damage burden of simultaneous cuts. Covers the p53-dependent G2-arrest mechanism, CRISPRcleanR (Iorio 2018) unsupervised pre-hoc correcti",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "990b52a5-b13a-48e6-807f-d81f51563fcf",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:32.115",
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Corrects the gene-independent copy-number artifact in CRISPR-Cas9 screens (Aguirre 2016 / Munoz 2016 Cancer Discov) where amplified loci appear essential from DNA-damage burden of simultaneous cuts. Covers the p53-dependent G2-arrest mechanism, CRISPRcleanR (Iorio 2018) unsupervised pre-hoc correcti",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "990b52a5-b13a-48e6-807f-d81f51563fcf",
        "enabled": 1,
        "created_by": "manish",
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    {
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      "id": 264,
      "workflow_bundle_id": "c187c886-44cc-486d-9f5f-96f94c3433c1",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "crispr_screens_crispresso_editing",
      "display_name": "CRISPR Screens Crispresso Editing",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Quantifies CRISPR editing outcomes with CRISPResso2 (Clement 2019 Nat Biotechnol) across Cas9-nuclease (indels, HDR), CBE and ABE base editors (target conversion + bystander), and prime editor (pegRNA-templated) modes. Covers single-amplicon (CRISPResso), multi-sample batch (CRISPRessoBatch), pooled",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
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      "created_at": "2026-06-08T01:57:33.915",
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        "engine": "nextflow",
        "name": "crispr_screens_crispresso_editing",
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c187c886-44cc-486d-9f5f-96f94c3433c1",
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        "created_by": "manish",
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      "category": "funcgen",
      "engine": "nextflow",
      "name": "crispr_screens_drugz_chemogenomic",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Analyzes CRISPR drug-modifier (chemogenomic) screens with drugZ (Li & Hart 2019 Genome Med), a bidirectional Z-score method that identifies synthetic-lethal sensitizing genes and resistance-conferring suppressor genes from vehicle vs drug comparisons. Covers vehicle-anchored design (not Day-0), the ",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
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      "created_at": "2026-06-08T01:57:35.745",
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        "configs": "[\"config/input.json\"]",
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
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      "id": 266,
      "workflow_bundle_id": "241cfd2b-604e-4812-92fb-ebbe5c6f70b0",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "crispr_screens_hit_calling",
      "display_name": "CRISPR Screens Hit Calling",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Cross-method decision tree for calling hits in pooled CRISPR screens. Catalogs statistical models (MAGeCK RRA, MAGeCK MLE, BAGEL2, drugZ, JACKS, Chronos, CERES), experimental designs each is built for, failure modes outside design domain, reconciliation when methods disagree, multiple-testing and ef",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "241cfd2b-604e-4812-92fb-ebbe5c6f70b0",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:37.553",
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        "engine": "nextflow",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Cross-method decision tree for calling hits in pooled CRISPR screens. Catalogs statistical models (MAGeCK RRA, MAGeCK MLE, BAGEL2, drugZ, JACKS, Chronos, CERES), experimental designs each is built for, failure modes outside design domain, reconciliation when methods disagree, multiple-testing and ef",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
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        "created_by": "manish",
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      "category": "funcgen",
      "engine": "nextflow",
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      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Designs and analyzes in vivo CRISPR screens in animal tumor models, organoids, and immune-cell adoptive transfers. Covers bottleneck math (250x cells/sgRNA requires ~25M cells implanted; impossible for most syngeneic models, forcing focused libraries), focused library design (Manguso 2017 Nature 547",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "e8710d32-9c73-434f-9fed-d9aeca74e071",
      "enabled": 1,
      "created_by": "manish",
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        "configs": "[\"config/input.json\"]",
        "description": "Designs and analyzes in vivo CRISPR screens in animal tumor models, organoids, and immune-cell adoptive transfers. Covers bottleneck math (250x cells/sgRNA requires ~25M cells implanted; impossible for most syngeneic models, forcing focused libraries), focused library design (Manguso 2017 Nature 547",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
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        "created_by": "manish",
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      "category": "funcgen",
      "engine": "nextflow",
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      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Runs JACKS (Joint Analysis of CRISPR/Cas9 Knockout Screens; Allen et al 2019 Genome Research) which models per-sgRNA log-fold-change as the product of a treatment-dependent gene-essentiality term and a treatment-independent guide-efficacy term. Covers the Bayesian decomposition math, the hierarchica",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
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      "created_at": "2026-06-08T01:57:41.231",
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
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      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Designs pooled sgRNA libraries for CRISPR knockout, interference (CRISPRi), activation (CRISPRa), Cas12a multiplex, base-editor, and prime-editor screens. Covers on-target scoring (Rule Set 2, Azimuth, DeepSpCas9, CRISPRon), off-target scoring (CFD, MIT), TSS-relative positioning for CRISPRi/a (Horl",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Designs pooled sgRNA libraries for CRISPR knockout, interference (CRISPRi), activation (CRISPRa), Cas12a multiplex, base-editor, and prime-editor screens. Covers on-target scoring (Rule Set 2, Azimuth, DeepSpCas9, CRISPRon), off-target scoring (CFD, MIT), TSS-relative positioning for CRISPRi/a (Horl",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
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      "category": "funcgen",
      "engine": "nextflow",
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      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Analyzes pooled CRISPR screens with MAGeCK (Li et al 2014), covering count generation (mageck count), the RRA two-condition workflow (mageck test using alpha-RRA over per-sgRNA negative-binomial p-values), the MLE multi-condition workflow (mageck mle with explicit design matrix and beta-score output",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "8c9f154c-8d73-41ea-83fc-03c334cb85e9",
      "enabled": 1,
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Analyzes pooled CRISPR screens with MAGeCK (Li et al 2014), covering count generation (mageck count), the RRA two-condition workflow (mageck test using alpha-RRA over per-sgRNA negative-binomial p-values), the MLE multi-condition workflow (mageck mle with explicit design matrix and beta-score output",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "8c9f154c-8d73-41ea-83fc-03c334cb85e9",
        "enabled": 1,
        "created_by": "manish",
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      "category": "funcgen",
      "engine": "nextflow",
      "name": "crispr_screens_perturb_seq_analysis",
      "display_name": "CRISPR Screens Perturb Seq Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Analyzes single-cell pooled CRISPR screens (Perturb-seq, CROP-seq, Perturb-CITE-seq, ECCITE-seq, multiome) where each cell carries an sgRNA and a scRNA-seq / surface-protein / chromatin readout. Covers experimental design (direct-capture Perturb-seq Dixit 2016 vs CROP-seq 3'UTR-barcoded Datlinger 20",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "ccdaba89-7eac-4732-bcdc-4acb06cd4bd7",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:57:46.808",
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        "display_name": "CRISPR Screens Perturb Seq Analysis",
        "version": "1.0.0",
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        "description": "Designs donor/repair templates for precise CRISPR knock-ins -- choosing the format (ssODN, long-ssDNA/Easi-CRISPR, dsDNA/plasmid, AAV6), sizing homology arms, placing the cut within ~10 bp of the edit, and adding a mandatory codon-checked blocking (PAM/seed) mutation so the edited allele is not re-c",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Detects focal chromatin loops (point interactions / corner-dots) in balanced Hi-C and Micro-C contact maps and aggregates/validates a loop set. Covers de-novo calling with cooltools dots (HiCCUPS-style 4-background local enrichment with lambda-chunked FDR), chromosight (template-correlation), and Mu",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "01d422d2-18a3-4a99-8c3e-84274b7a25e3",
        "enabled": 1,
        "created_by": "manish",
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    {
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      "category": "funcgen",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "MAGeCK CRISPR screen analysis with read counting, gene-level testing, and pathway enrichment",
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      "container_image": null,
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "MAGeCK CRISPR screen analysis with read counting, gene-level testing, and pathway enrichment",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "42cd12b1-c392-4bd2-92e0-3f11d7fd52b0",
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    {
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      "id": 350,
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      "category": "funcgen",
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      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Balances Hi-C contact matrices (ICE via cooler.balance_cooler, KR/SCALE/VC context), computes distance-decay expected with cooltools (expected_cis per-diagonal P(s), expected_trans scalar), builds observed/expected (O/E) matrices, and diagnoses polymer state from the P(s) log-derivative. Covers the ",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "5d707f1f-0287-4cf5-b13f-ad75f92326d0",
      "enabled": 1,
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        "engine": "nextflow",
        "name": "matrix_operations",
        "display_name": "Matrix Operations",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Balances Hi-C contact matrices (ICE via cooler.balance_cooler, KR/SCALE/VC context), computes distance-decay expected with cooltools (expected_cis per-diagonal P(s), expected_trans scalar), builds observed/expected (O/E) matrices, and diagnoses polymer state from the P(s) log-derivative. Covers the ",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "5d707f1f-0287-4cf5-b13f-ad75f92326d0",
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        "created_by": "manish",
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    {
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      "category": "funcgen",
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      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Decompose total effects into direct and indirect paths through mediators using mediation, CMAverse 4-way, HIMA/HIMA2 high-dimensional, BAMA, two-step / MVMR mediation, or double-ML medDML. Use when testing whether a molecular phenotype (expression, methylation, protein) mediates a treatment-outcome ",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "780cd49a-709a-439c-93d5-9b6b48ea4841",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:55:27.355",
      "raw": {
        "id": 195,
        "category": "funcgen",
        "engine": "nextflow",
        "name": "mediation_analysis",
        "display_name": "Mediation Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Decompose total effects into direct and indirect paths through mediators using mediation, CMAverse 4-way, HIMA/HIMA2 high-dimensional, BAMA, two-step / MVMR mediation, or double-ML medDML. Use when testing whether a molecular phenotype (expression, methylation, protein) mediates a treatment-outcome ",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "780cd49a-709a-439c-93d5-9b6b48ea4841",
        "enabled": 1,
        "created_by": "manish",
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    {
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      "id": 179,
      "workflow_bundle_id": "840a9d41-c6ff-4bb5-bdc7-5726f7f91624",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "mendelian_randomization",
      "display_name": "Mendelian Randomization with TwoSampleMR",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Mendelian randomization causal inference with TwoSampleMR and sensitivity analysis",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "840a9d41-c6ff-4bb5-bdc7-5726f7f91624",
      "enabled": 1,
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        "category": "funcgen",
        "engine": "nextflow",
        "name": "mendelian_randomization",
        "display_name": "Mendelian Randomization with TwoSampleMR",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Mendelian randomization causal inference with TwoSampleMR and sensitivity analysis",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "840a9d41-c6ff-4bb5-bdc7-5726f7f91624",
        "enabled": 1,
        "created_by": "manish",
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    {
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      "id": 124,
      "workflow_bundle_id": "7a7398f4-c2de-44f1-90ea-4d7b366b26d0",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "micro_c",
      "display_name": "Micro-C / Hi-C",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "distiller-nf processing, cooler binning, TAD calling, and loop detection",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": "docker.io/man4ish/omnibioai-funcgen:1.0",
      "object_id": "7a7398f4-c2de-44f1-90ea-4d7b366b26d0",
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      "created_by": "manish",
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      "raw": {
        "id": 124,
        "category": "funcgen",
        "engine": "nextflow",
        "name": "micro_c",
        "display_name": "Micro-C / Hi-C",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "distiller-nf processing, cooler binning, TAD calling, and loop detection",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-funcgen:1.0",
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        "created_by": "manish",
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    {
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      "id": 333,
      "workflow_bundle_id": "7cb042ef-b8c2-430c-93e5-5d668fcc7dd2",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "off_target_prediction",
      "display_name": "Off Target Prediction",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Nominates and assesses CRISPR off-target sites genome-wide. Enumerates candidate sites by mismatch and bulge tolerance with Cas-OFFinder/CRISPRitz, ranks them with the published CFD score (SpCas9-only, relative ranker) or MIT/CRISTA/energy models, runs variant-aware screening against gnomAD/individu",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "7cb042ef-b8c2-430c-93e5-5d668fcc7dd2",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:59:40.025",
      "raw": {
        "id": 333,
        "category": "funcgen",
        "engine": "nextflow",
        "name": "off_target_prediction",
        "display_name": "Off Target Prediction",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Nominates and assesses CRISPR off-target sites genome-wide. Enumerates candidate sites by mismatch and bulge tolerance with Cas-OFFinder/CRISPRitz, ranks them with the published CFD score (SpCas9-only, relative ranker) or MIT/CRISTA/energy models, runs variant-aware screening against gnomAD/individu",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "7cb042ef-b8c2-430c-93e5-5d668fcc7dd2",
        "enabled": 1,
        "created_by": "manish",
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    {
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      "id": 242,
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      "category": "funcgen",
      "engine": "nextflow",
      "name": "ortholog_inference",
      "display_name": "Ortholog Inference",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Infer orthologous genes and gene families across species using OrthoFinder3 (HOG-based phylogenetic orthology), SonicParanoid2, Broccoli, ProteinOrtho, OMA / FastOMA hierarchical orthologous groups, eggNOG-mapper, JustOrthologs, and TOGA whole-genome-alignment orthology. Use when building single-cop",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "440b5432-7324-47f1-8239-419da0b7a725",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:56:53.324",
      "raw": {
        "id": 242,
        "category": "funcgen",
        "engine": "nextflow",
        "name": "ortholog_inference",
        "display_name": "Ortholog Inference",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Infer orthologous genes and gene families across species using OrthoFinder3 (HOG-based phylogenetic orthology), SonicParanoid2, Broccoli, ProteinOrtho, OMA / FastOMA hierarchical orthologous groups, eggNOG-mapper, JustOrthologs, and TOGA whole-genome-alignment orthology. Use when building single-cop",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "440b5432-7324-47f1-8239-419da0b7a725",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:56:53.324"
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    },
    {
      "source": "workflow_registry",
      "id": 341,
      "workflow_bundle_id": "904b3800-81ba-49e6-afe9-443e0cc45332",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "overlap_significance",
      "display_name": "Overlap Significance",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Tests whether two genomic interval sets overlap (colocalize) more than expected by chance using a permutation test against a structured-genome null model. Covers bedtools fisher (analytic 2x2 screen), bedtools shuffle + jaccard permutation, GAT (isochore/GC-conditioned simulation with FDR), regioneR",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "904b3800-81ba-49e6-afe9-443e0cc45332",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:59:54.830",
      "raw": {
        "id": 341,
        "category": "funcgen",
        "engine": "nextflow",
        "name": "overlap_significance",
        "display_name": "Overlap Significance",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Tests whether two genomic interval sets overlap (colocalize) more than expected by chance using a permutation test against a structured-genome null model. Covers bedtools fisher (analytic 2x2 screen), bedtools shuffle + jaccard permutation, GAT (isochore/GC-conditioned simulation with FDR), regioneR",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "904b3800-81ba-49e6-afe9-443e0cc45332",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:59:54.830"
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    {
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      "id": 243,
      "workflow_bundle_id": "f66e6c7b-e9ef-474f-b688-29d8065fa6fd",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "pangenome_analysis",
      "display_name": "Pangenome Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Build and analyze pangenomes for prokaryotes (Panaroo, PPanGGOLiN, PEPPAN, GET_HOMOLOGUES, anvi'o pangenomics) and eukaryotes (Minigraph-Cactus, PGGB, vg pangenome graphs). Implement Tettelin core/accessory/cloud genome decomposition (Tettelin 2005), Heap's law open/closed pangenome modeling, gene p",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "f66e6c7b-e9ef-474f-b688-29d8065fa6fd",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:56:55.183",
      "raw": {
        "id": 243,
        "category": "funcgen",
        "engine": "nextflow",
        "name": "pangenome_analysis",
        "display_name": "Pangenome Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Build and analyze pangenomes for prokaryotes (Panaroo, PPanGGOLiN, PEPPAN, GET_HOMOLOGUES, anvi'o pangenomics) and eukaryotes (Minigraph-Cactus, PGGB, vg pangenome graphs). Implement Tettelin core/accessory/cloud genome decomposition (Tettelin 2005), Heap's law open/closed pangenome modeling, gene p",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "f66e6c7b-e9ef-474f-b688-29d8065fa6fd",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:56:55.183"
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    {
      "source": "workflow_registry",
      "id": 178,
      "workflow_bundle_id": "be3522ef-ce46-4079-8a87-9f2d60c2ab20",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "perturbseq",
      "display_name": "Perturb-seq Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Perturb-seq analysis with Cell Ranger CRISPR counting and Pertpy perturbation analysis",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "be3522ef-ce46-4079-8a87-9f2d60c2ab20",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:49:14.015",
      "raw": {
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        "category": "funcgen",
        "engine": "nextflow",
        "name": "perturbseq",
        "display_name": "Perturb-seq Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Perturb-seq analysis with Cell Ranger CRISPR counting and Pertpy perturbation analysis",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "be3522ef-ce46-4079-8a87-9f2d60c2ab20",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:49:14.015"
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    {
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      "id": 196,
      "workflow_bundle_id": "f6780998-ca2a-46c5-bc46-81cedad7a9fe",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "pleiotropy_detection",
      "display_name": "Pleiotropy Detection",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Detect and adjust for horizontal pleiotropy in two-sample Mendelian randomization by distinguishing uncorrelated (UHP) from correlated (CHP) pleiotropy and choosing among Egger, MR-PRESSO, MR-RAPS, CAUSE, LHC-MR, LCV, MR-Clust, MR-Mix, and contamination-mixture methods. Use when validating an MR cau",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "f6780998-ca2a-46c5-bc46-81cedad7a9fe",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:55:29.151",
      "raw": {
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        "category": "funcgen",
        "engine": "nextflow",
        "name": "pleiotropy_detection",
        "display_name": "Pleiotropy Detection",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Detect and adjust for horizontal pleiotropy in two-sample Mendelian randomization by distinguishing uncorrelated (UHP) from correlated (CHP) pleiotropy and choosing among Egger, MR-PRESSO, MR-RAPS, CAUSE, LHC-MR, LCV, MR-Clust, MR-Mix, and contamination-mixture methods. Use when validating an MR cau",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "f6780998-ca2a-46c5-bc46-81cedad7a9fe",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:55:29.151"
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    {
      "source": "workflow_registry",
      "id": 417,
      "workflow_bundle_id": "c3785045-5c5b-42ce-9e19-408cb3c029d4",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "plink_basics",
      "display_name": "Plink Basics",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "PLINK file formats, format conversion, and quality control filtering for population genetics. Convert between VCF, BED/BIM/FAM, and PED/MAP formats, apply MAF, genotyping rate, and HWE filters using PLINK 1.9 and 2.0. Use when working with PLINK format files or running QC.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "c3785045-5c5b-42ce-9e19-408cb3c029d4",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:02:21.814",
      "raw": {
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        "category": "funcgen",
        "engine": "nextflow",
        "name": "plink_basics",
        "display_name": "Plink Basics",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "PLINK file formats, format conversion, and quality control filtering for population genetics. Convert between VCF, BED/BIM/FAM, and PED/MAP formats, apply MAF, genotyping rate, and HWE filters using PLINK 1.9 and 2.0. Use when working with PLINK format files or running QC.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c3785045-5c5b-42ce-9e19-408cb3c029d4",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:02:21.814"
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      "id": 80,
      "workflow_bundle_id": "665f5316-8fab-4ec8-9020-78f080ba8f85",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "polygenic_risk_score_v1",
      "display_name": "Polygenic Risk Score (PRS)",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Polygenic Risk Score calculation pipeline for disease risk prediction. Performs VCF validation, variant QC (MAF, HWE, missingness), GWAS harmonization, LD clumping/thresholding, PRS computation as weighted allele sum, score normalization, population percentile assignment, risk group stratification, and model calibration.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "665f5316-8fab-4ec8-9020-78f080ba8f85",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-23T01:04:43.345",
      "raw": {
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        "category": "funcgen",
        "engine": "nextflow",
        "name": "polygenic_risk_score_v1",
        "display_name": "Polygenic Risk Score (PRS)",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Polygenic Risk Score calculation pipeline for disease risk prediction. Performs VCF validation, variant QC (MAF, HWE, missingness), GWAS harmonization, LD clumping/thresholding, PRS computation as weighted allele sum, score normalization, population percentile assignment, risk group stratification, and model calibration.",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "665f5316-8fab-4ec8-9020-78f080ba8f85",
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        "created_by": "manish",
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      "workflow_bundle_id": "2b8951bb-22f2-4fcf-990c-bb8eaea0b22d",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "population_genetics_v1",
      "display_name": "Population Genetics Analysis Pipeline",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Population genetics pipeline: VCF filtering (MAF, missingness, HWE), LD pruning, PCA, ADMIXTURE (K=2-4), pairwise Fst, iHS selection sweep detection, and NJ phylogeny.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "2b8951bb-22f2-4fcf-990c-bb8eaea0b22d",
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      "created_by": "manish",
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        "engine": "nextflow",
        "name": "population_genetics_v1",
        "display_name": "Population Genetics Analysis Pipeline",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Population genetics pipeline: VCF filtering (MAF, missingness, HWE), LD pruning, PCA, ADMIXTURE (K=2-4), pairwise Fst, iHS selection sweep detection, and NJ phylogeny.",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "2b8951bb-22f2-4fcf-990c-bb8eaea0b22d",
        "enabled": 1,
        "created_by": "manish",
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      "id": 418,
      "workflow_bundle_id": "d84ad59c-02f1-44f2-beb0-5315c64d8a5a",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "population_structure",
      "display_name": "Population Structure",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Analyze population structure using PCA and admixture analysis with PLINK and ADMIXTURE. Identify population clusters, assess ancestry proportions, visualize genetic structure, and choose optimal K for admixture models. Use when analyzing population stratification with PCA or admixture.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d84ad59c-02f1-44f2-beb0-5315c64d8a5a",
      "enabled": 1,
      "created_by": "manish",
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        "engine": "nextflow",
        "name": "population_structure",
        "display_name": "Population Structure",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Analyze population structure using PCA and admixture analysis with PLINK and ADMIXTURE. Identify population clusters, assess ancestry proportions, visualize genetic structure, and choose optimal K for admixture models. Use when analyzing population stratification with PCA or admixture.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d84ad59c-02f1-44f2-beb0-5315c64d8a5a",
        "enabled": 1,
        "created_by": "manish",
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      "id": 244,
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      "category": "funcgen",
      "engine": "nextflow",
      "name": "positive_selection",
      "display_name": "Positive Selection",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Detect positive (diversifying / episodic / pervasive) selection using codon dN/dS frameworks. Implements PAML codeml site models (M0/M1a/M2a/M7/M8/M8a), branch models, branch-site model A (Zhang 2005), and HyPhy methods (BUSTED, BUSTED-S, BUSTED-MH, BUSTED-PH, MEME, FEL, FUBAR, aBSREL, SLAC, RELAX, ",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "8f93d9be-0955-4849-b60a-98c88f379a9d",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:56:56.974",
      "raw": {
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        "engine": "nextflow",
        "name": "positive_selection",
        "display_name": "Positive Selection",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Detect positive (diversifying / episodic / pervasive) selection using codon dN/dS frameworks. Implements PAML codeml site models (M0/M1a/M2a/M7/M8/M8a), branch models, branch-site model A (Zhang 2005), and HyPhy methods (BUSTED, BUSTED-S, BUSTED-MH, BUSTED-PH, MEME, FEL, FUBAR, aBSREL, SLAC, RELAX, ",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "8f93d9be-0955-4849-b60a-98c88f379a9d",
        "enabled": 1,
        "created_by": "manish",
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      "id": 334,
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      "category": "funcgen",
      "engine": "nextflow",
      "name": "prime_editing_design",
      "display_name": "Prime Editing Design",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Designs pegRNAs and nicking guides for prime editing (PE) -- choosing the nick/strand, tuning the primer-binding site (PBS) and reverse-transcription template (RTT) as a per-locus panel, selecting the PE system (PE2/PE3/PE3b/PE4/PE5/PEmax/PE7), adding MMR-evading and PAM-disrupting silent edits, app",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "4a035f99-7054-43d2-bd1b-eeb7829b3dd3",
      "enabled": 1,
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      "created_at": "2026-06-08T01:59:41.909",
      "raw": {
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        "engine": "nextflow",
        "name": "prime_editing_design",
        "display_name": "Prime Editing Design",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Designs pegRNAs and nicking guides for prime editing (PE) -- choosing the nick/strand, tuning the primer-binding site (PBS) and reverse-transcription template (RTT) as a per-locus panel, selecting the PE system (PE2/PE3/PE3b/PE4/PE5/PEmax/PE7), adding MMR-evading and PAM-disrupting silent edits, app",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
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      "id": 197,
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      "category": "funcgen",
      "engine": "nextflow",
      "name": "proteome_mr_drug_target",
      "display_name": "Proteome MR Drug Target",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Runs cis-pQTL Mendelian randomization for drug-target validation using UKB-PPP (Olink), deCODE (SomaScan), Fenland, INTERVAL, ARIC, and FinnGen-PPP proteomes plus colocalization triangulation, phenome-wide on-target adverse-effect scans, cross-platform Olink/SomaScan replication, and PAV (protein-al",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "7ca5b5f8-c0d5-46d0-87ea-3f3f18797242",
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        "engine": "nextflow",
        "name": "proteome_mr_drug_target",
        "display_name": "Proteome MR Drug Target",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Runs cis-pQTL Mendelian randomization for drug-target validation using UKB-PPP (Olink), deCODE (SomaScan), Fenland, INTERVAL, ARIC, and FinnGen-PPP proteomes plus colocalization triangulation, phenome-wide on-target adverse-effect scans, cross-platform Olink/SomaScan replication, and PAV (protein-al",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "7ca5b5f8-c0d5-46d0-87ea-3f3f18797242",
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      "workflow_bundle_id": "45762423-149b-4ee7-aef3-7d0d86b1e4ab",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "proximity_operations",
      "display_name": "Proximity Operations",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Performs proximity operations on genomic intervals with bedtools (closest, window, flank, slop) and pybedtools - nearest-feature queries with signed/strand-aware distance, fixed-radius window searches, strand-aware promoter construction, and interval extension. Covers the closest -d/-D a/b/ref/-t/-k",
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      "outputs": "[]",
      "container_image": null,
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        "engine": "nextflow",
        "name": "proximity_operations",
        "display_name": "Proximity Operations",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Performs proximity operations on genomic intervals with bedtools (closest, window, flank, slop) and pybedtools - nearest-feature queries with signed/strand-aware distance, fixed-radius window searches, strand-aware promoter construction, and interval extension. Covers the closest -d/-D a/b/ref/-t/-k",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "45762423-149b-4ee7-aef3-7d0d86b1e4ab",
        "enabled": 1,
        "created_by": "manish",
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    {
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      "id": 414,
      "workflow_bundle_id": "a0bb2570-e40b-4044-8597-65b60f984786",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "reference_panels",
      "display_name": "Reference Panels",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Download, prepare, and manage reference panels for phasing and imputation. Covers 1000 Genomes, HRC, and TOPMed panels. Use when setting up imputation infrastructure or selecting appropriate reference panels for target populations.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "a0bb2570-e40b-4044-8597-65b60f984786",
      "enabled": 1,
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        "engine": "nextflow",
        "name": "reference_panels",
        "display_name": "Reference Panels",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Download, prepare, and manage reference panels for phasing and imputation. Covers 1000 Genomes, HRC, and TOPMed panels. Use when setting up imputation infrastructure or selecting appropriate reference panels for target populations.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "a0bb2570-e40b-4044-8597-65b60f984786",
        "enabled": 1,
        "created_by": "manish",
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      "id": 419,
      "workflow_bundle_id": "e568b0a9-2b06-4e83-8ec3-bbe66e0d02b3",
      "category": "funcgen",
      "engine": "nextflow",
      "name": "scikit_allel_analysis",
      "display_name": "Scikit Allel Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Python population genetics with scikit-allel. Read VCF files, compute allele frequencies, calculate diversity statistics, perform PCA, and run selection scans using GenotypeArray and HaplotypeArray data structures. Use when analyzing population genetics in Python.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "e568b0a9-2b06-4e83-8ec3-bbe66e0d02b3",
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      "created_by": "manish",
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        "category": "funcgen",
        "engine": "nextflow",
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        "display_name": "Scikit Allel Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Python population genetics with scikit-allel. Read VCF files, compute allele frequencies, calculate diversity statistics, perform PCA, and run selection scans using GenotypeArray and HaplotypeArray data structures. Use when analyzing population genetics in Python.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "e568b0a9-2b06-4e83-8ec3-bbe66e0d02b3",
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        "created_by": "manish",
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      "category": "funcgen",
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      "display_name": "Selection Statistics",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Detect signatures of natural selection using Fst, Tajima's D, iHS, XP-EHH, and other selection statistics. Calculate population differentiation, test for departures from neutrality, and identify selective sweeps with scikit-allel and vcftools. Use when computing selection signatures like Fst or Taji",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "16d4842c-8c83-422c-9e46-fb49e51123c9",
      "enabled": 1,
      "created_by": "manish",
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      "raw": {
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        "category": "funcgen",
        "engine": "nextflow",
        "name": "selection_statistics",
        "display_name": "Selection Statistics",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Detect signatures of natural selection using Fst, Tajima's D, iHS, XP-EHH, and other selection statistics. Calculate population differentiation, test for departures from neutrality, and identify selective sweeps with scikit-allel and vcftools. Use when computing selection signatures like Fst or Taji",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "16d4842c-8c83-422c-9e46-fb49e51123c9",
        "enabled": 1,
        "created_by": "manish",
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      "id": 245,
      "workflow_bundle_id": "c7ae9d58-5b57-41fa-bd1e-a3009f12ff11",
      "category": "funcgen",
      "engine": "nextflow",
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      "display_name": "Synteny Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Detect syntenic blocks and structural rearrangements between genomes using MCScanX (Wang 2012), JCVI/MCScan (Tang 2008 Python), GENESPACE (Lovell 2022) for orthology-anchored riparian visualization, SyRI for structural variation, AnchorWave for sequence-level synteny, i-ADHoRe 3.0 for highly diverge",
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      "container_image": null,
      "object_id": "c7ae9d58-5b57-41fa-bd1e-a3009f12ff11",
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        "engine": "nextflow",
        "name": "synteny_analysis",
        "display_name": "Synteny Analysis",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Detect syntenic blocks and structural rearrangements between genomes using MCScanX (Wang 2012), JCVI/MCScan (Tang 2008 Python), GENESPACE (Lovell 2022) for orthology-anchored riparian visualization, SyRI for structural variation, AnchorWave for sequence-level synteny, i-ADHoRe 3.0 for highly diverge",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "c7ae9d58-5b57-41fa-bd1e-a3009f12ff11",
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      "category": "funcgen",
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      "name": "tad_detection",
      "display_name": "TAD Detection with cooltools",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Topologically associating domain (TAD) detection with cooltools insulation score and boundary calling",
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      "outputs": "[]",
      "container_image": null,
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        "display_name": "TAD Detection with cooltools",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Topologically associating domain (TAD) detection with cooltools insulation score and boundary calling",
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        "outputs": "[]",
        "container_image": null,
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      "workflow_bundle_id": "c3d72466-3ba3-413e-bcaf-9bd984da24eb",
      "category": "funcgen",
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      "name": "transcriptome_wide_association",
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      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Performs gene-level association from GWAS summary statistics via genetically predicted tissue expression using FUSION, PrediXcan, S-PrediXcan, S-MultiXcan, UTMOST, MOSTWAS, kTWAS, EpiXcan, TIGAR-V2, and probabilistic fine-mapping with FOCUS and MA-FOCUS. Use when running TWAS from GWAS sumstats, pri",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "c3d72466-3ba3-413e-bcaf-9bd984da24eb",
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        "engine": "nextflow",
        "name": "transcriptome_wide_association",
        "display_name": "Transcriptome Wide Association",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Performs gene-level association from GWAS summary statistics via genetically predicted tissue expression using FUSION, PrediXcan, S-PrediXcan, S-MultiXcan, UTMOST, MOSTWAS, kTWAS, EpiXcan, TIGAR-V2, and probabilistic fine-mapping with FOCUS and MA-FOCUS. Use when running TWAS from GWAS sumstats, pri",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c3d72466-3ba3-413e-bcaf-9bd984da24eb",
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        "created_by": "manish",
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      "id": 126,
      "workflow_bundle_id": "7dfee20a-9b16-4ec9-b14f-7581c7bb453a",
      "category": "funcgen",
      "engine": "nextflow",
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      "description": "Assembles microbial-community sequencing into metagenome-assembled genomes (MAGs) with metaFlye (ONT), metaSPAdes/MEGAHIT (Illumina), and hifiasm-meta/metaMDBG (PacBio HiFi), then recovers genomes via multi-binner consolidation (MetaBAT2, MaxBin2, CONCOCT, SemiBin2, VAMB -> DAS_Tool) and QCs them ag",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d4b3d5f4-42f9-4a4e-b777-fca882f8196f",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Assembles microbial-community sequencing into metagenome-assembled genomes (MAGs) with metaFlye (ONT), metaSPAdes/MEGAHIT (Illumina), and hifiasm-meta/metaMDBG (PacBio HiFi), then recovers genomes via multi-binner consolidation (MetaBAT2, MaxBin2, CONCOCT, SemiBin2, VAMB -> DAS_Tool) and QCs them ag",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d4b3d5f4-42f9-4a4e-b777-fca882f8196f",
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        "created_by": "manish",
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      "name": "nanopore_assembly",
      "display_name": "Nanopore Assembly",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Flye de-novo assembly, Medaka polishing, QUAST assembly QC, and BUSCO completeness",
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      "container_image": "docker.io/man4ish/omnibioai-longread:1.0",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Flye de-novo assembly, Medaka polishing, QUAST assembly QC, and BUSCO completeness",
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        "outputs": "[]",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Nanopore de novo assembly with Flye, Medaka polishing, and QUAST/BUSCO quality assessment",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "adecd83e-70c1-453b-b1e5-2acf7fe9f668",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Nanopore de novo assembly with Flye, Medaka polishing, and QUAST/BUSCO quality assessment",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "adecd83e-70c1-453b-b1e5-2acf7fe9f668",
        "enabled": 1,
        "created_by": "manish",
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      "id": 171,
      "workflow_bundle_id": "5e1dc95f-d85a-427f-9051-9ef2b2bf004a",
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      "name": "nanopore_basecalling",
      "display_name": "Nanopore Basecalling with Dorado",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Nanopore basecalling with Dorado including adapter trimming and read quality statistics",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "5e1dc95f-d85a-427f-9051-9ef2b2bf004a",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Nanopore basecalling with Dorado including adapter trimming and read quality statistics",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "5e1dc95f-d85a-427f-9051-9ef2b2bf004a",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:49:01.337"
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      "workflow_bundle_id": "5b92fb4c-400c-4be7-af5f-9857ff6172b8",
      "category": "longread",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Dorado modkit 5mC+5hmC detection and differential methylation region calling",
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      "outputs": "[]",
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      "created_by": "manish",
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        "category": "longread",
        "engine": "nextflow",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Dorado modkit 5mC+5hmC detection and differential methylation region calling",
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        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-longread:1.0",
        "object_id": "5b92fb4c-400c-4be7-af5f-9857ff6172b8",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-05T23:05:39.518"
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      "source": "workflow_registry",
      "id": 112,
      "workflow_bundle_id": "6ff8b4f1-158c-4c64-a930-568ef67f0999",
      "category": "longread",
      "engine": "nextflow",
      "name": "nanopore_direct_rna",
      "display_name": "Nanopore Direct RNA",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "minimap2 alignment, NanoCount isoform quantification, and m6A modification detection",
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      "container_image": "docker.io/man4ish/omnibioai-longread:1.0",
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        "category": "longread",
        "engine": "nextflow",
        "name": "nanopore_direct_rna",
        "display_name": "Nanopore Direct RNA",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "minimap2 alignment, NanoCount isoform quantification, and m6A modification detection",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-longread:1.0",
        "object_id": "6ff8b4f1-158c-4c64-a930-568ef67f0999",
        "enabled": 1,
        "created_by": "manish",
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      "workflow_bundle_id": "9db4a81d-d2e8-4f59-b841-6aa15a6d1eb9",
      "category": "longread",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Calls DNA methylation from Oxford Nanopore sequencing data using signal-level analysis. Use when detecting 5mC or 6mA modifications directly from nanopore reads without bisulfite conversion.",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "9db4a81d-d2e8-4f59-b841-6aa15a6d1eb9",
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        "display_name": "Nanopore Methylation",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Calls DNA methylation from Oxford Nanopore sequencing data using signal-level analysis. Use when detecting 5mC or 6mA modifications directly from nanopore reads without bisulfite conversion.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "9db4a81d-d2e8-4f59-b841-6aa15a6d1eb9",
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        "created_by": "manish",
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      "workflow_bundle_id": "49e84800-d26d-415e-8662-6144ebd743a6",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Nanopore long-read methylation analysis pipeline for 5mC and 5hmC detection. Performs read QC, minimap2 alignment, base modification calling, haplotype-aware methylation phasing, CpG profiling, differentially methylated region (DMR) detection, allele-specific methylation, and structural variant detection with methylation context.",
      "inputs_schema": null,
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      "container_image": null,
      "object_id": "49e84800-d26d-415e-8662-6144ebd743a6",
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        "display_name": "Nanopore Long-Read Methylation",
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        "entrypoint": "workflow/main.nf",
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        "description": "Nanopore long-read methylation analysis pipeline for 5mC and 5hmC detection. Performs read QC, minimap2 alignment, base modification calling, haplotype-aware methylation phasing, CpG profiling, differentially methylated region (DMR) detection, allele-specific methylation, and structural variant detection with methylation context.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "49e84800-d26d-415e-8662-6144ebd743a6",
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      "workflow_bundle_id": "c61152f1-43d4-4239-b756-e317bfab711f",
      "category": "longread",
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      "display_name": "Nanopore Methylation Calling v2",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Nanopore methylation calling with modkit pileup and summary statistics",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "c61152f1-43d4-4239-b756-e317bfab711f",
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Nanopore methylation calling with modkit pileup and summary statistics",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c61152f1-43d4-4239-b756-e317bfab711f",
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      "category": "longread",
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      "display_name": "PacBio HiFi",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "pbmm2 alignment, DeepVariant SNP/indel calling, PBSV SV detection, WhatsHap phasing",
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      "container_image": "docker.io/man4ish/omnibioai-longread:1.0",
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        "category": "longread",
        "engine": "nextflow",
        "name": "pacbio_hifi",
        "display_name": "PacBio HiFi",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "pbmm2 alignment, DeepVariant SNP/indel calling, PBSV SV detection, WhatsHap phasing",
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        "container_image": "docker.io/man4ish/omnibioai-longread:1.0",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "PacBio HiFi de novo assembly with hifiasm, GFA to FASTA conversion, and QUAST/BUSCO quality assessment",
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      "container_image": null,
      "object_id": "500a67a7-3d06-4398-a7f1-3a40cd1fcddf",
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        "display_name": "PacBio HiFi Assembly with hifiasm",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "PacBio HiFi de novo assembly with hifiasm, GFA to FASTA conversion, and QUAST/BUSCO quality assessment",
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        "container_image": null,
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Pangenome graph construction and analysis pipeline for core/accessory genome identification, variant calling, and phylogeny.",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "79a3bae8-a021-406e-8ae6-ddd4ccef5e56",
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        "entrypoint": "workflow/main.nf",
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        "description": "Pangenome graph construction and analysis pipeline for core/accessory genome identification, variant calling, and phylogeny.",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "79a3bae8-a021-406e-8ae6-ddd4ccef5e56",
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      "category": "longread",
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      "name": "scaffolding",
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      "entrypoint": "workflow/main.nf",
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      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "6134682a-70fa-41cd-9d08-4871868c28a3",
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        "category": "longread",
        "engine": "nextflow",
        "name": "scaffolding",
        "display_name": "Scaffolding",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Orders and orients assembled contigs into chromosome-scale scaffolds from long-range linking data, inserting N-gap spacers (adds no sequence). Covers Hi-C/Omni-C scaffolding (YaHS, SALSA2, 3D-DNA/Juicer), Hi-C read-mapping prerequisites (map each end separately, no mate rescue, dedup, enzyme-aware),",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "6134682a-70fa-41cd-9d08-4871868c28a3",
        "enabled": 1,
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      "category": "longread",
      "engine": "nextflow",
      "name": "short_read_assembly",
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      "entrypoint": "workflow/main.nf",
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      "container_image": null,
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        "display_name": "Short Read Assembly",
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        "container_image": null,
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        "description": "Species abundance estimation using Bracken with Kraken2 output. Redistributes reads from higher taxonomic levels to species for more accurate estimates. Use when accurate species-level abundances are needed from Kraken2 classification output.",
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      "description": "Amplicon sequence variant (ASV) inference from 16S rRNA or ITS amplicon sequencing using DADA2. Covers quality filtering, error learning, denoising, and chimera removal. Use when processing demultiplexed amplicon FASTQ files to generate an ASV table for downstream analysis.",
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        "entrypoint": "workflow/main.nf",
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        "description": "Amplicon sequence variant (ASV) inference from 16S rRNA or ITS amplicon sequencing using DADA2. Covers quality filtering, error learning, denoising, and chimera removal. Use when processing demultiplexed amplicon FASTQ files to generate an ASV table for downstream analysis.",
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        "container_image": null,
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      "category": "microbiome",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "AMR gene detection with Flye/SPAdes assembly, AMRFinderPlus, and CARD RGI",
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      "container_image": null,
      "object_id": "bc833b8f-5484-492a-be50-a9eb44726cb6",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "AMR gene detection with Flye/SPAdes assembly, AMRFinderPlus, and CARD RGI",
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        "container_image": null,
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      "workflow_bundle_id": "107e9b42-5e0d-4181-9e76-55eaed946f36",
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      "display_name": "AMR Genomic Surveillance",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Epidemiological surveillance of antimicrobial resistance using WGS and phylodynamics.",
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      "container_image": null,
      "object_id": "107e9b42-5e0d-4181-9e76-55eaed946f36",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Epidemiological surveillance of antimicrobial resistance using WGS and phylodynamics.",
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        "container_image": null,
        "object_id": "107e9b42-5e0d-4181-9e76-55eaed946f36",
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      "workflow_bundle_id": "b640ab2f-1e54-4ed7-b73b-9d69e9cadaf9",
      "category": "microbiome",
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      "name": "claw_metagenomics",
      "display_name": "Claw Metagenomics",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Shotgun metagenomics profiling with CLAW pipeline: taxonomy classification, resistome, and functional pathways.",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "b640ab2f-1e54-4ed7-b73b-9d69e9cadaf9",
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        "engine": "nextflow",
        "name": "claw_metagenomics",
        "display_name": "Claw Metagenomics",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Shotgun metagenomics profiling with CLAW pipeline: taxonomy classification, resistome, and functional pathways.",
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        "outputs": "[]",
        "container_image": null,
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Differential abundance testing for microbiome data using compositionally-aware methods like ALDEx2, ANCOM-BC2, and MaAsLin2. Use when identifying taxa that differ between experimental groups while accounting for the compositional nature of microbiome data.",
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      "container_image": null,
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Differential abundance testing for microbiome data using compositionally-aware methods like ALDEx2, ANCOM-BC2, and MaAsLin2. Use when identifying taxa that differ between experimental groups while accounting for the compositional nature of microbiome data.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "288a0955-f9b2-4dd5-99fb-0e332fe6fce7",
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        "created_by": "manish",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Alpha and beta diversity analysis for microbiome data. Calculate within-sample richness, evenness, and between-sample dissimilarity with phyloseq and vegan. Use when comparing community composition across samples or testing for group differences in microbiome structure.",
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      "container_image": null,
      "object_id": "340b54d1-bf25-4a70-9dba-4229c08063f8",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Alpha and beta diversity analysis for microbiome data. Calculate within-sample richness, evenness, and between-sample dissimilarity with phyloseq and vegan. Use when comparing community composition across samples or testing for group differences in microbiome structure.",
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        "container_image": null,
        "object_id": "340b54d1-bf25-4a70-9dba-4229c08063f8",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Predict metagenome functional content from 16S rRNA marker gene data using PICRUSt2. Infer KEGG, MetaCyc, and EC abundances from ASV tables. Use when functional profiling is needed from 16S data without shotgun metagenomics sequencing.",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Predict metagenome functional content from 16S rRNA marker gene data using PICRUSt2. Infer KEGG, MetaCyc, and EC abundances from ASV tables. Use when functional profiling is needed from 16S data without shotgun metagenomics sequencing.",
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      "configs": "[\"config/input.json\"]",
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        "configs": "[\"config/input.json\"]",
        "description": "Metagenomic functional profiling with HUMAnN3 including normalization and pathway regrouping",
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        "container_image": null,
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        "description": "Analyze associations between microbiome composition and cancer phenotypes.",
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        "container_image": null,
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        "description": "QIIME2 command-line workflow for 16S/ITS amplicon analysis. Alternative to DADA2/phyloseq R workflow with built-in provenance tracking. Use when preferring CLI over R, needing reproducible provenance, or working within QIIME2 ecosystem.",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Microbial strain tracking with MASH distance estimation and inStrain population genetics",
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      "container_image": null,
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Microbial strain tracking with MASH distance estimation and inStrain population genetics",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Access and analyze AlphaFold protein structure predictions. Use when predicted structures are needed for proteins without experimental structures, or for confidence scores (pLDDT).",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "2abbb98e-e540-4991-8256-f94daa2fd4dc",
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      "created_by": "manish",
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        "category": "multimodal",
        "engine": "nextflow",
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        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "2abbb98e-e540-4991-8256-f94daa2fd4dc",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:59:08.996"
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    },
    {
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      "id": 317,
      "workflow_bundle_id": "b14f4fb2-f6e9-4430-900b-9d318d014eab",
      "category": "multimodal",
      "engine": "nextflow",
      "name": "genome_annotation_functional_annotation",
      "display_name": "Genome Annotation Functional Annotation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Assigns GO terms, Pfam/InterPro domains, KEGG orthologs, EC numbers, and product names to predicted proteins using eggNOG-mapper (orthology), InterProScan (domain signatures), and KofamScan (KEGG), routing specialized functions to dbCAN/antiSMASH/AMRFinderPlus/SignalP. Covers the orthology-vs-domain",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "b14f4fb2-f6e9-4430-900b-9d318d014eab",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:59:10.825",
      "raw": {
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        "category": "multimodal",
        "engine": "nextflow",
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        "display_name": "Genome Annotation Functional Annotation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Assigns GO terms, Pfam/InterPro domains, KEGG orthologs, EC numbers, and product names to predicted proteins using eggNOG-mapper (orthology), InterProScan (domain signatures), and KofamScan (KEGG), routing specialized functions to dbCAN/antiSMASH/AMRFinderPlus/SignalP. Covers the orthology-vs-domain",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "b14f4fb2-f6e9-4430-900b-9d318d014eab",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:59:10.825"
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    },
    {
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      "id": 318,
      "workflow_bundle_id": "41a473e0-a9df-4e9f-ba3f-e2de08216c56",
      "category": "multimodal",
      "engine": "nextflow",
      "name": "genome_annotation_ncrna_annotation",
      "display_name": "Genome Annotation NCRNA Annotation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
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      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "41a473e0-a9df-4e9f-ba3f-e2de08216c56",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:59:12.661",
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        "category": "multimodal",
        "engine": "nextflow",
        "name": "genome_annotation_ncrna_annotation",
        "display_name": "Genome Annotation NCRNA Annotation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "41a473e0-a9df-4e9f-ba3f-e2de08216c56",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:59:12.661"
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    {
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      "id": 319,
      "workflow_bundle_id": "129b35a8-f5c3-4636-acbd-d18586dfa20a",
      "category": "multimodal",
      "engine": "nextflow",
      "name": "genome_annotation_prokaryotic_annotation",
      "display_name": "Genome Annotation Prokaryotic Annotation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Annotates bacterial and archaeal genomes (isolates, MAGs, plasmids) with Bakta (active versioned databases, NCBI-compliant output) or Prokka (legacy), producing GFF3/GenBank/EMBL/FASTA with INSDC locus tags. Covers Bakta-vs-Prokka-vs-PGAP-vs-DFAST choice, light-vs-full database tiers, translation-ta",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "129b35a8-f5c3-4636-acbd-d18586dfa20a",
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        "engine": "nextflow",
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        "display_name": "Genome Annotation Prokaryotic Annotation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "129b35a8-f5c3-4636-acbd-d18586dfa20a",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:59:14.468"
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    },
    {
      "source": "workflow_registry",
      "id": 320,
      "workflow_bundle_id": "f6fff721-446a-427e-8056-be6c47c5397b",
      "category": "multimodal",
      "engine": "nextflow",
      "name": "genome_annotation_repeat_annotation",
      "display_name": "Genome Annotation Repeat Annotation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Discovers, classifies, and masks repetitive elements and transposable elements with RepeatModeler2 (de novo family library), RepeatMasker (masking against a library), EDTA (plant/structural TEs), or EarlGrey (auto-curating wrapper), and quantifies TE expression from RNA-seq with TEtranscripts/SQuIRE",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "f6fff721-446a-427e-8056-be6c47c5397b",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:59:16.318",
      "raw": {
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        "category": "multimodal",
        "engine": "nextflow",
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        "display_name": "Genome Annotation Repeat Annotation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Discovers, classifies, and masks repetitive elements and transposable elements with RepeatModeler2 (de novo family library), RepeatMasker (masking against a library), EDTA (plant/structural TEs), or EarlGrey (auto-curating wrapper), and quantifies TE expression from RNA-seq with TEtranscripts/SQuIRE",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "f6fff721-446a-427e-8056-be6c47c5397b",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T01:59:16.318"
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    },
    {
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      "id": 480,
      "workflow_bundle_id": "38144ff2-1103-4049-bf72-f9cff710aa59",
      "category": "multimodal",
      "engine": "nextflow",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Perform geometric calculations on protein structures using Biopython Bio.PDB. Use when measuring distances, angles, and dihedrals, superimposing structures, calculating RMSD, or computing solvent accessible surface area (SASA).",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "38144ff2-1103-4049-bf72-f9cff710aa59",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:04:16.468",
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        "category": "multimodal",
        "engine": "nextflow",
        "name": "geometric_analysis",
        "display_name": "Geometric Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Perform geometric calculations on protein structures using Biopython Bio.PDB. Use when measuring distances, angles, and dihedrals, superimposing structures, calculating RMSD, or computing solvent accessible surface area (SASA).",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "38144ff2-1103-4049-bf72-f9cff710aa59",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:04:16.468"
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    {
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      "id": 583,
      "workflow_bundle_id": "c55a65ed-d7b3-4189-96ac-67de55c83896",
      "category": "multimodal",
      "engine": "nextflow",
      "name": "histolab_wsi",
      "display_name": "Whole Slide Image Processing",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Process whole slide images (WSI) for pathology analysis using histolab tile extraction.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "c55a65ed-d7b3-4189-96ac-67de55c83896",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:33:45.689",
      "raw": {
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        "category": "multimodal",
        "engine": "nextflow",
        "name": "histolab_wsi",
        "display_name": "Whole Slide Image Processing",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Process whole slide images (WSI) for pathology analysis using histolab tile extraction.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "c55a65ed-d7b3-4189-96ac-67de55c83896",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:33:45.689"
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    {
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      "id": 70,
      "workflow_bundle_id": "1d4a1d36-0527-4fb8-ae95-c80c65dbf1a7",
      "category": "multimodal",
      "engine": "nextflow",
      "name": "immune_deconvolution_v1",
      "display_name": "Immune Cell Deconvolution",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Immune cell deconvolution pipeline for tumor microenvironment analysis using CIBERSORT, xCell, and TIMER with survival analysis and immunophenoscore.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "1d4a1d36-0527-4fb8-ae95-c80c65dbf1a7",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-22T21:55:29.679",
      "raw": {
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        "category": "multimodal",
        "engine": "nextflow",
        "name": "immune_deconvolution_v1",
        "display_name": "Immune Cell Deconvolution",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Immune cell deconvolution pipeline for tumor microenvironment analysis using CIBERSORT, xCell, and TIMER with survival analysis and immunophenoscore.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "1d4a1d36-0527-4fb8-ae95-c80c65dbf1a7",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-05-22T21:55:29.679"
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    {
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      "id": 535,
      "workflow_bundle_id": "42a6f789-9cc3-41c9-b3f7-6710c17c3c65",
      "category": "multimodal",
      "engine": "nextflow",
      "name": "kegg_pathway_query",
      "display_name": "Kegg Pathway Query",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Access KEGG pathway, compound, and enzyme databases via REST API for pathway analysis.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "42a6f789-9cc3-41c9-b3f7-6710c17c3c65",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:09:44.308",
      "raw": {
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        "category": "multimodal",
        "engine": "nextflow",
        "name": "kegg_pathway_query",
        "display_name": "Kegg Pathway Query",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Access KEGG pathway, compound, and enzyme databases via REST API for pathway analysis.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "42a6f789-9cc3-41c9-b3f7-6710c17c3c65",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:09:44.308"
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    {
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      "id": 381,
      "workflow_bundle_id": "1ebd25a4-bdc7-4e23-a2bf-4db85f9e7f3b",
      "category": "multimodal",
      "engine": "nextflow",
      "name": "lipidomics",
      "display_name": "Lipidomics",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Specialized lipidomics analysis for lipid identification, quantification, and pathway interpretation. Covers LC-MS lipidomics with LipidSearch, MS-DIAL, and LipidMaps annotation. Use when analyzing lipid classes, chain composition, or lipid-specific pathways.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "1ebd25a4-bdc7-4e23-a2bf-4db85f9e7f3b",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:01:15.622",
      "raw": {
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        "category": "multimodal",
        "engine": "nextflow",
        "name": "lipidomics",
        "display_name": "Lipidomics",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Specialized lipidomics analysis for lipid identification, quantification, and pathway interpretation. Covers LC-MS lipidomics with LipidSearch, MS-DIAL, and LipidMaps annotation. Use when analyzing lipid classes, chain composition, or lipid-specific pathways.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "1ebd25a4-bdc7-4e23-a2bf-4db85f9e7f3b",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:01:15.622"
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    {
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      "id": 588,
      "workflow_bundle_id": "d020d5f9-5cc6-4123-af0d-c4c9218babf2",
      "category": "multimodal",
      "engine": "nextflow",
      "name": "mesh_generation",
      "display_name": "3D Mesh Generation and Processing",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Generate and process 3D meshes for molecular visualization and structural biology.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d020d5f9-5cc6-4123-af0d-c4c9218babf2",
      "enabled": 1,
      "created_by": "manish",
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      "raw": {
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        "engine": "nextflow",
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        "display_name": "3D Mesh Generation and Processing",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Generate and process 3D meshes for molecular visualization and structural biology.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d020d5f9-5cc6-4123-af0d-c4c9218babf2",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:33:54.835"
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    {
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      "workflow_bundle_id": "749b2b73-7f17-4ac0-81d1-7cf69a6af757",
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      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Build genome-scale metabolic models from genome sequences using CarveMe and gapseq for automated reconstruction. Generate draft models ready for curation and analysis. Use when creating metabolic models for organisms without existing models.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "749b2b73-7f17-4ac0-81d1-7cf69a6af757",
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        "display_name": "Metabolic Reconstruction",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Build genome-scale metabolic models from genome sequences using CarveMe and gapseq for automated reconstruction. Generate draft models ready for curation and analysis. Use when creating metabolic models for organisms without existing models.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "749b2b73-7f17-4ac0-81d1-7cf69a6af757",
        "enabled": 1,
        "created_by": "manish",
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      "workflow_bundle_id": "d2f8cc66-c2aa-4d8a-a69f-d67317ad637e",
      "category": "multimodal",
      "engine": "nextflow",
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      "display_name": "Metabolite Annotation",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Metabolite identification from m/z and retention time. Covers database matching, MS/MS spectral matching, and confidence level assignment. Use when assigning compound identities to detected features in untargeted metabolomics.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d2f8cc66-c2aa-4d8a-a69f-d67317ad637e",
      "enabled": 1,
      "created_by": "manish",
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      "raw": {
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        "engine": "nextflow",
        "name": "metabolite_annotation",
        "display_name": "Metabolite Annotation",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Metabolite identification from m/z and retention time. Covers database matching, MS/MS spectral matching, and confidence level assignment. Use when assigning compound identities to detected features in untargeted metabolomics.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d2f8cc66-c2aa-4d8a-a69f-d67317ad637e",
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        "created_by": "manish",
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      "workflow_bundle_id": "08f75eef-e603-4baa-bfdb-edaaf9dee324",
      "category": "multimodal",
      "engine": "nextflow",
      "name": "metabolomics_lcms",
      "display_name": "Metabolomics LC-MS",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "XCMS peak detection, MZmine3 alignment, and pathway annotation for LC-MS metabolomics",
      "inputs_schema": null,
      "outputs": "[]",
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        "description": "Statistical analysis for metabolomics data. Covers preprocessing (log2 transformation, normalization), limma moderated testing with empirical Bayes, Welch's t-tests with BH correction, fold change estimation, and multivariate methods (PCA, PLS-DA, OPLS-DA). Use when identifying differentially abunda",
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        "description": "Modify protein structures using Biopython Bio.PDB. Use when transforming coordinates, removing atoms or residues, adding new entities, modifying B-factors and occupancies, or building structures programmatically.",
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      "container_image": null,
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        "description": "Statistical testing for differentially abundant proteins between conditions. Covers preprocessing (log2 transformation, normalization), limma and DEqMS workflows with empirical Bayes moderation, fold change shrinkage for accurate effect size estimation, and Python alternatives. Use when identifying ",
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        "description": "Peptide-spectrum matching and protein identification from MS/MS data. Use when identifying peptides from tandem mass spectra. Covers database searching, spectral library matching, and FDR estimation using target-decoy approaches.",
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        "description": "Protein grouping and inference from peptide identifications. Use when resolving protein ambiguity from shared peptides. Handles protein groups and protein-level FDR control using parsimony and probabilistic approaches.",
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        "description": "Predict protein structures using ESMFold or AlphaFold2 with confidence assessment.",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Design protein sequences for given backbone structures using ProteinMPNN inverse folding.",
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        "entrypoint": "workflow/main.nf",
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    {
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      "category": "proteomics",
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    {
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      "category": "proteomics",
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      "description": "Mass spectrometry-based proteomics pipeline with database search, FDR filtering, protein quantification, and pathway enrichment analysis.",
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        "container_image": null,
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      "entrypoint": "workflow/main.nf",
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        "entrypoint": "workflow/main.nf",
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        "description": "Quality control and assessment for proteomics data. Use when evaluating proteomics data quality before downstream analysis. Covers sample metrics, missing value patterns, replicate correlation, batch effects, and intensity distributions.",
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        "outputs": "[]",
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      "description": "Post-translational modification analysis including phosphorylation, acetylation, and ubiquitination. Covers site localization, motif analysis, and quantitative PTM analysis. Use when analyzing phosphoproteomic data or other modification-enriched samples.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
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        "entrypoint": "workflow/main.nf",
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        "description": "Post-translational modification analysis including phosphorylation, acetylation, and ubiquitination. Covers site localization, motif analysis, and quantitative PTM analysis. Use when analyzing phosphoproteomic data or other modification-enriched samples.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "7190c813-bfc9-4d80-8f2a-25bb01ca5a54",
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      "workflow_bundle_id": "94e21139-75d9-4d0a-8a00-69383f314aa5",
      "category": "proteomics",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Protein quantification from mass spectrometry data including label-free (LFQ, intensity-based), isobaric labeling (TMT, iTRAQ), and metabolic labeling (SILAC) approaches. Use when extracting protein abundances from MS data for differential analysis.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "94e21139-75d9-4d0a-8a00-69383f314aa5",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:02:47.242",
      "raw": {
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        "engine": "nextflow",
        "name": "quantification",
        "display_name": "Quantification",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Protein quantification from mass spectrometry data including label-free (LFQ, intensity-based), isobaric labeling (TMT, iTRAQ), and metabolic labeling (SILAC) approaches. Use when extracting protein abundances from MS data for differential analysis.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "94e21139-75d9-4d0a-8a00-69383f314aa5",
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        "created_by": "manish",
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    {
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      "workflow_bundle_id": "f735c522-2e46-4446-8e77-759924e804f3",
      "category": "proteomics",
      "engine": "nextflow",
      "name": "rfdiffusion_binder",
      "display_name": "RFdiffusion Binder Design",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "De novo protein binder design using RFdiffusion diffusion-based backbone generation.",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "f735c522-2e46-4446-8e77-759924e804f3",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:32:37.547",
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        "category": "proteomics",
        "engine": "nextflow",
        "name": "rfdiffusion_binder",
        "display_name": "RFdiffusion Binder Design",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "De novo protein binder design using RFdiffusion diffusion-based backbone generation.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "f735c522-2e46-4446-8e77-759924e804f3",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:32:37.547"
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    {
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      "workflow_bundle_id": "e342e60e-9e70-4f3d-8235-3cbd99fe327b",
      "category": "proteomics",
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      "name": "spectral_libraries",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Build, manage, and search spectral libraries for proteomics. Use when creating or working with spectral libraries for DIA analysis. Covers DDA-based library generation, predicted libraries (Prosit, DeepLC), and library formats.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "e342e60e-9e70-4f3d-8235-3cbd99fe327b",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Build, manage, and search spectral libraries for proteomics. Use when creating or working with spectral libraries for DIA analysis. Covers DDA-based library generation, predicted libraries (Prosit, DeepLC), and library formats.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "e342e60e-9e70-4f3d-8235-3cbd99fe327b",
        "enabled": 1,
        "created_by": "manish",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "pLink2 cross-linked peptide identification and protein interaction topology mapping",
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      "object_id": "a68a21e0-a6a1-4904-9934-e042cacd23af",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "pLink2 cross-linked peptide identification and protein interaction topology mapping",
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        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-proteomics:1.0",
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      "entrypoint": "workflow/main.nf",
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        "entrypoint": "workflow/main.nf",
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      "entrypoint": "workflow/main.nf",
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        "entrypoint": "workflow/main.nf",
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      "configs": "[\"config/input.json\"]",
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        "entrypoint": "workflow/main.nf",
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        "description": "Discover novel miRNAs and quantify known miRNAs using miRDeep2 de novo prediction.",
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        "container_image": null,
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      "configs": "[\"config/input.json\"]",
      "description": "ORF detection from Ribo-seq data using RiboCode with metaplots and full ORF calling",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "ORF detection from Ribo-seq data using RiboCode with metaplots and full ORF calling",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "2361ccf4-9d1f-45d6-84c8-869874bde5ac",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Detects aberrant splicing in single rare-disease patients vs a control panel using FRASER 2.0 (Bioconductor; Beta-binomial autoencoder on Intron Jaccard Index, default delta cutoff 0.1, q hyperparameter), OUTRIDER (gene-level outlier expression via autoencoder denoising), LeafcutterMD (Dirichlet-mul",
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      "outputs": "[]",
      "container_image": null,
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        "engine": "nextflow",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
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        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "4dc75ae1-cf2a-41f5-abf5-8bb7eb5e77ad",
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      "display_name": "PyDESeq2 Differential Expression",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Differential gene expression analysis in Python using PyDESeq2 Wald tests with FDR correction.",
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      "outputs": "[]",
      "container_image": null,
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        "display_name": "PyDESeq2 Differential Expression",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Differential gene expression analysis in Python using PyDESeq2 Wald tests with FDR correction.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "bdde4a0d-509b-40fb-b63b-4783d073ed51",
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      "workflow_bundle_id": "d3648046-53f6-4c50-b4b0-e290fe48056b",
      "category": "rnaseq",
      "engine": "nextflow",
      "name": "pydeseq2_dge",
      "display_name": "Pydeseq2 Dge",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Differential gene expression analysis using PyDESeq2 (Python DESeq2), Wald tests, and FDR correction.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "d3648046-53f6-4c50-b4b0-e290fe48056b",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:09:12.695",
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        "engine": "nextflow",
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        "display_name": "Pydeseq2 Dge",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Differential gene expression analysis using PyDESeq2 (Python DESeq2), Wald tests, and FDR correction.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "d3648046-53f6-4c50-b4b0-e290fe48056b",
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        "created_by": "manish",
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      "id": 162,
      "workflow_bundle_id": "71937318-42e8-41df-9c7a-291c7ebe5c22",
      "category": "rnaseq",
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      "display_name": "Ribo-seq Preprocessing",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Ribo-seq preprocessing with adapter trimming, rRNA removal, STAR alignment, and P-site analysis",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "71937318-42e8-41df-9c7a-291c7ebe5c22",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T01:48:45.143",
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        "category": "rnaseq",
        "engine": "nextflow",
        "name": "riboseq_preprocessing",
        "display_name": "Ribo-seq Preprocessing",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Ribo-seq preprocessing with adapter trimming, rRNA removal, STAR alignment, and P-site analysis",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "71937318-42e8-41df-9c7a-291c7ebe5c22",
        "enabled": 1,
        "created_by": "manish",
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      "id": 60,
      "workflow_bundle_id": "68baf6ed-2b79-4c97-a3c0-2a161ac33f6d",
      "category": "rnaseq",
      "engine": "nextflow",
      "name": "riboseq_v1",
      "display_name": "Ribo-seq Analysis",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Ribosome profiling pipeline for translation efficiency analysis, ORF discovery, and differential translation using Ribo-seq data.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "68baf6ed-2b79-4c97-a3c0-2a161ac33f6d",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-22T21:41:33.092",
      "raw": {
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        "category": "rnaseq",
        "engine": "nextflow",
        "name": "riboseq_v1",
        "display_name": "Ribo-seq Analysis",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "Ribosome profiling pipeline for translation efficiency analysis, ORF discovery, and differential translation using Ribo-seq data.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "68baf6ed-2b79-4c97-a3c0-2a161ac33f6d",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-05-22T21:41:33.092"
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    {
      "source": "workflow_registry",
      "id": 448,
      "workflow_bundle_id": "5e4e5f8c-f8d5-406e-86e1-4762c97250bf",
      "category": "rnaseq",
      "engine": "nextflow",
      "name": "ribosome_periodicity",
      "display_name": "Ribosome Periodicity",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Validate Ribo-seq data quality by checking 3-nucleotide periodicity and calculating P-site offsets. Use when assessing library quality or determining read offsets for downstream analysis.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "5e4e5f8c-f8d5-406e-86e1-4762c97250bf",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:18.223",
      "raw": {
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        "category": "rnaseq",
        "engine": "nextflow",
        "name": "ribosome_periodicity",
        "display_name": "Ribosome Periodicity",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Validate Ribo-seq data quality by checking 3-nucleotide periodicity and calculating P-site offsets. Use when assessing library quality or determining read offsets for downstream analysis.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "5e4e5f8c-f8d5-406e-86e1-4762c97250bf",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:18.223"
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    {
      "source": "workflow_registry",
      "id": 449,
      "workflow_bundle_id": "bffa3465-b801-4d2f-a81c-024029f76c09",
      "category": "rnaseq",
      "engine": "nextflow",
      "name": "ribosome_stalling",
      "display_name": "Ribosome Stalling",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Detect ribosome pausing and stalling sites from Ribo-seq data at codon resolution. Use when studying translational regulation, identifying pause sites, or analyzing codon-specific translation dynamics.",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "bffa3465-b801-4d2f-a81c-024029f76c09",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-06-08T02:03:20.024",
      "raw": {
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        "category": "rnaseq",
        "engine": "nextflow",
        "name": "ribosome_stalling",
        "display_name": "Ribosome Stalling",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Detect ribosome pausing and stalling sites from Ribo-seq data at codon resolution. Use when studying translational regulation, identifying pause sites, or analyzing codon-specific translation dynamics.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "bffa3465-b801-4d2f-a81c-024029f76c09",
        "enabled": 1,
        "created_by": "manish",
        "created_at": "2026-06-08T02:03:20.024"
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      "source": "workflow_registry",
      "id": 75,
      "workflow_bundle_id": "73804918-5762-4547-a948-b1cc72240dd4",
      "category": "rnaseq",
      "engine": "nextflow",
      "name": "rna_editing_v1",
      "display_name": "RNA Editing Detection",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "RNA editing detection pipeline for A-to-I and C-to-U editing sites using STAR 2-pass alignment, GATK variant calling, dbSNP filtering, and ADAR target analysis.",
      "inputs_schema": "{\"dbsnp\": {\"type\": \"string\", \"description\": \"dbSNP VCF for filtering\"}, \"input\": {\"type\": \"string\", \"description\": \"Samplesheet CSV\"}, \"genome\": {\"type\": \"string\", \"description\": \"Reference genome FASTA\"}, \"outdir\": {\"type\": \"string\", \"description\": \"Output directory\"}, \"annotation\": {\"type\": \"string\", \"description\": \"Gene annotation GTF\"}, \"editing_type\": {\"type\": \"string\", \"description\": \"A_to_I or C_to_U\"}}",
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      "container_image": null,
      "object_id": "73804918-5762-4547-a948-b1cc72240dd4",
      "enabled": 1,
      "created_by": "manish",
      "created_at": "2026-05-23T00:16:24.462",
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        "category": "rnaseq",
        "engine": "nextflow",
        "name": "rna_editing_v1",
        "display_name": "RNA Editing Detection",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
        "description": "RNA editing detection pipeline for A-to-I and C-to-U editing sites using STAR 2-pass alignment, GATK variant calling, dbSNP filtering, and ADAR target analysis.",
        "inputs_schema": "{\"dbsnp\": {\"type\": \"string\", \"description\": \"dbSNP VCF for filtering\"}, \"input\": {\"type\": \"string\", \"description\": \"Samplesheet CSV\"}, \"genome\": {\"type\": \"string\", \"description\": \"Reference genome FASTA\"}, \"outdir\": {\"type\": \"string\", \"description\": \"Output directory\"}, \"annotation\": {\"type\": \"string\", \"description\": \"Gene annotation GTF\"}, \"editing_type\": {\"type\": \"string\", \"description\": \"A_to_I or C_to_U\"}}",
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        "container_image": null,
        "object_id": "73804918-5762-4547-a948-b1cc72240dd4",
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        "created_by": "manish",
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      "workflow_bundle_id": "491dfda1-2dd0-4229-920b-8c09efcb934b",
      "category": "rnaseq",
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      "name": "rnaseq_nextflow_v1",
      "display_name": "RNA-seq (Nextflow) v1",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "RNA-seq Nextflow workflow (multisample): trim (skewer) + quant (kallisto)",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "491dfda1-2dd0-4229-920b-8c09efcb934b",
      "enabled": 1,
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "RNA-seq Nextflow workflow (multisample): trim (skewer) + quant (kallisto)",
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        "outputs": "[]",
        "container_image": null,
        "object_id": "491dfda1-2dd0-4229-920b-8c09efcb934b",
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      "category": "rnaseq",
      "engine": "nextflow",
      "name": "rnaseq_v1",
      "display_name": "RNA-seq v1",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/nextflow.config\"]",
      "description": "Test RNA-seq pipeline (Nextflow)",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "object://workflows/rnaseq/rnaseq_v1/1.0.0",
      "enabled": 1,
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/nextflow.config\"]",
        "description": "Test RNA-seq pipeline (Nextflow)",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "object://workflows/rnaseq/rnaseq_v1/1.0.0",
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        "created_by": "manish",
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      "workflow_bundle_id": "7fdd85c7-e71a-4f9f-8d5c-a48440f3592b",
      "category": "rnaseq",
      "engine": "nextflow",
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      "entrypoint": "workflow/main.nf",
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      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "7fdd85c7-e71a-4f9f-8d5c-a48440f3592b",
      "enabled": 1,
      "created_by": "manish",
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        "category": "rnaseq",
        "engine": "nextflow",
        "name": "sashimi_plots",
        "display_name": "Sashimi Plots",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Creates sashimi-style plots showing RNA-seq read coverage and splice junction counts using ggsashimi (general-purpose, condition-grouped overlays), rmats2sashimiplot (rMATS-output-aware), MAJIQ-VOILA (LSV posteriors interactive HTML), leafviz (leafcutter clusters Shiny), Jutils (tool-agnostic heatma",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "7fdd85c7-e71a-4f9f-8d5c-a48440f3592b",
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        "created_by": "manish",
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      "id": 456,
      "workflow_bundle_id": "75d8ba66-3a0b-4a64-8984-d540e4416dca",
      "category": "rnaseq",
      "engine": "nextflow",
      "name": "secondary_structure_prediction",
      "display_name": "Secondary Structure Prediction",
      "version": "1.0.0",
      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Predicts RNA secondary structures using minimum free energy folding and partition function analysis with ViennaRNA (RNAfold, RNAalifold, RNAcofold). Computes base-pair probabilities, centroid structures, and consensus structures from alignments. Use when predicting RNA folding, evaluating structural",
      "inputs_schema": null,
      "outputs": "[]",
      "container_image": null,
      "object_id": "75d8ba66-3a0b-4a64-8984-d540e4416dca",
      "enabled": 1,
      "created_by": "manish",
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        "category": "rnaseq",
        "engine": "nextflow",
        "name": "secondary_structure_prediction",
        "display_name": "Secondary Structure Prediction",
        "version": "1.0.0",
        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Predicts RNA secondary structures using minimum free energy folding and partition function analysis with ViennaRNA (RNAfold, RNAalifold, RNAcofold). Computes base-pair probabilities, centroid structures, and consensus structures from alignments. Use when predicting RNA folding, evaluating structural",
        "inputs_schema": null,
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        "container_image": null,
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        "description": "Harmony, scVI, and BBKNN batch correction benchmark for scRNA-seq",
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      "description": "Quality control for scRNA-seq using MAD-based filtering and scverse best practices.",
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        "configs": "[\"config/input.json\"]",
        "description": "Quality control for scRNA-seq using MAD-based filtering and scverse best practices.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "de229e2f-3612-4e71-8bd5-4e3776224376",
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      "configs": "[\"config/input.json\"]",
      "description": "Single-cell RNA-seq quality control with scater: per-cell QC metrics, outlier detection, and visualization.",
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      "outputs": "[]",
      "container_image": null,
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        "description": "Single-cell RNA-seq quality control with scater: per-cell QC metrics, outlier detection, and visualization.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
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      "configs": "[\"config/input.json\"]",
      "description": "cellranger-vdj and scirpy clonotype tracking and repertoire diversity analysis",
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        "configs": "[\"config/input.json\"]",
        "description": "cellranger-vdj and scirpy clonotype tracking and repertoire diversity analysis",
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        "outputs": "[]",
        "container_image": "docker.io/man4ish/omnibioai-singlecell:1.0",
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      "id": 520,
      "workflow_bundle_id": "2994b54e-3561-4927-a7c6-a9dc9eea99ad",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "RNA velocity analysis with scVelo: estimate cell state transitions from unspliced/spliced mRNA dynamics.",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "2994b54e-3561-4927-a7c6-a9dc9eea99ad",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "RNA velocity analysis with scVelo: estimate cell state transitions from unspliced/spliced mRNA dynamics.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "2994b54e-3561-4927-a7c6-a9dc9eea99ad",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "Estimate RNA velocity from unspliced/spliced mRNA dynamics to infer cell state transitions.",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "34e86d1d-7283-45b6-a99a-34d0415b7b52",
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      "created_by": "manish",
      "created_at": "2026-06-08T02:34:33.142",
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        "category": "singlecell",
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        "name": "scvelo_velocity",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "Estimate RNA velocity from unspliced/spliced mRNA dynamics to infer cell state transitions.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "34e86d1d-7283-45b6-a99a-34d0415b7b52",
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        "created_by": "manish",
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      "id": 519,
      "workflow_bundle_id": "486bf4d0-39ac-45a6-b660-4fae99b515a0",
      "category": "singlecell",
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      "name": "seurat_scrna",
      "display_name": "Seurat Scrna",
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      "entrypoint": "workflow/main.nf",
      "configs": "[\"config/input.json\"]",
      "description": "scRNA-seq analysis with Seurat v5: QC, normalization, clustering, UMAP, and marker gene identification.",
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      "outputs": "[]",
      "container_image": null,
      "object_id": "486bf4d0-39ac-45a6-b660-4fae99b515a0",
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        "display_name": "Seurat Scrna",
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        "entrypoint": "workflow/main.nf",
        "configs": "[\"config/input.json\"]",
        "description": "scRNA-seq analysis with Seurat v5: QC, normalization, clustering, UMAP, and marker gene identification.",
        "inputs_schema": null,
        "outputs": "[]",
        "container_image": null,
        "object_id": "486bf4d0-39ac-45a6-b660-4fae99b515a0",
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      "description": "10x Genomics Multiome analysis pipeline combining scRNA-seq and scATAC-seq from the same cell. Performs joint QC, TF-IDF and scran normalization, LSI/PCA dimensionality reduction, WNN integration, joint Leiden clustering, cell type annotation, gene activity scoring, TF motif enrichment, peak-gene linkage, and regulatory network inference.",
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        "description": "10x Genomics Multiome analysis pipeline combining scRNA-seq and scATAC-seq from the same cell. Performs joint QC, TF-IDF and scran normalization, LSI/PCA dimensionality reduction, WNN integration, joint Leiden clustering, cell type annotation, gene activity scoring, TF motif enrichment, peak-gene linkage, and regulatory network inference.",
        "inputs_schema": null,
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        "container_image": null,
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      "configs": "[\"config/base.config\", \"config/docker.config\", \"config/test.config\"]",
      "description": "Single-cell V(D)J immune repertoire analysis pipeline for TCR/BCR sequencing with clonotype calling, diversity metrics, clonal expansion, CDR3 analysis, and GEX integration.",
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        "description": "Single-cell V(D)J immune repertoire analysis pipeline for TCR/BCR sequencing with clonotype calling, diversity metrics, clonal expansion, CDR3 analysis, and GEX integration.",
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