Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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Per-region pindel
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![]() Path: definitions/subworkflows/pindel_cat.cwl Branch/Commit ID: a08de598edc04f340fdbff76c9a92336a7702022 |
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process VCF workflow
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![]() Path: definitions/subworkflows/strelka_process_vcf.cwl Branch/Commit ID: a08de598edc04f340fdbff76c9a92336a7702022 |
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gathered exome alignment and somatic variant detection
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![]() Path: definitions/pipelines/somatic_exome_gathered.cwl Branch/Commit ID: 2e0562a5c3cd7aac24af4c622a5ae68a7fb23a71 |
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varscan somatic workflow
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![]() Path: definitions/subworkflows/varscan.cwl Branch/Commit ID: a08de598edc04f340fdbff76c9a92336a7702022 |
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umi molecular alignment workflow
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![]() Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: 2979b565f88ceebca934611adbf3fb8cefd65a19 |
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phase VCF
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![]() Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: 2979b565f88ceebca934611adbf3fb8cefd65a19 |
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workflow.cwl
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![]() Path: flow_md5checksums/workflow.cwl Branch/Commit ID: 0b58c250e8ab7c5efae29443f08ea74316127041 |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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![]() Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 2979b565f88ceebca934611adbf3fb8cefd65a19 |
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RNA-Seq alignment and transcript/gene abundance workflow
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![]() Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
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Detect DoCM variants
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![]() Path: definitions/subworkflows/docm_germline.cwl Branch/Commit ID: f42c889734c8f709ad2fd9090493bcaac8326c98 |