Explore Workflows
View already parsed workflows here or click here to add your own
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Bisulfite QC tools
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![]() Path: definitions/subworkflows/bisulfite_qc.cwl Branch/Commit ID: 9cbf2a483e1b9e4cdb8e2564be27a9e64fc1169e |
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exome alignment and somatic variant detection for cle purpose
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![]() Path: definitions/pipelines/somatic_exome_cle.cwl Branch/Commit ID: 2979b565f88ceebca934611adbf3fb8cefd65a19 |
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wgs alignment and germline variant detection
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![]() Path: definitions/pipelines/germline_wgs.cwl Branch/Commit ID: 2979b565f88ceebca934611adbf3fb8cefd65a19 |
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somatic_exome: exome alignment and somatic variant detection
somatic_exome is designed to perform processing of mutant/wildtype H.sapiens exome sequencing data. It features BQSR corrected alignments, 4 caller variant detection, and vep style annotations. Structural variants are detected via manta and cnvkit. In addition QC metrics are run, including somalier concordance metrics. example input file = analysis_workflows/example_data/somatic_exome.yaml |
![]() Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: 2979b565f88ceebca934611adbf3fb8cefd65a19 |
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umi per-lane alignment subworkflow
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![]() Path: definitions/subworkflows/umi_alignment.cwl Branch/Commit ID: 9cbf2a483e1b9e4cdb8e2564be27a9e64fc1169e |
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Bisulfite alignment and QC
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![]() Path: definitions/pipelines/bisulfite.cwl Branch/Commit ID: 2979b565f88ceebca934611adbf3fb8cefd65a19 |
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Detect Variants workflow for WGS pipeline
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![]() Path: definitions/pipelines/detect_variants_wgs.cwl Branch/Commit ID: 389f6edccab082d947bee9c032f59dbdf9f7c325 |
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allele-process-strain.cwl
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![]() Path: subworkflows/allele-process-strain.cwl Branch/Commit ID: 3e2ad9c049ea96584c365559c687205e3b642146 |
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gdc_dnaseq.bamfastq_align.workflow.cwl
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![]() Path: workflows/gdc_dnaseq.bamfastq_align.workflow.cwl Branch/Commit ID: b8f00532dfccc9bfdbfa4236e615e5a49bf97d9f |
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Downsample and HaplotypeCaller
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![]() Path: definitions/pipelines/downsample_and_recall.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |