Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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umi per-lane alignment subworkflow
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/umi_alignment.cwl Branch/Commit ID: 9cbf2a483e1b9e4cdb8e2564be27a9e64fc1169e |
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Bisulfite alignment and QC
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https://github.com/genome/analysis-workflows.git
Path: definitions/pipelines/bisulfite.cwl Branch/Commit ID: 2979b565f88ceebca934611adbf3fb8cefd65a19 |
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Detect Variants workflow for WGS pipeline
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https://github.com/genome/analysis-workflows.git
Path: definitions/pipelines/detect_variants_wgs.cwl Branch/Commit ID: 389f6edccab082d947bee9c032f59dbdf9f7c325 |
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allele-process-strain.cwl
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https://github.com/Barski-lab/workflows.git
Path: subworkflows/allele-process-strain.cwl Branch/Commit ID: 3e2ad9c049ea96584c365559c687205e3b642146 |
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gdc_dnaseq.bamfastq_align.workflow.cwl
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https://github.com/NCI-GDC/gdc-dnaseq-cwl.git
Path: workflows/gdc_dnaseq.bamfastq_align.workflow.cwl Branch/Commit ID: b8f00532dfccc9bfdbfa4236e615e5a49bf97d9f |
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Downsample and HaplotypeCaller
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https://github.com/genome/analysis-workflows.git
Path: definitions/pipelines/downsample_and_recall.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |
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format_rrnas_from_seq_entry
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https://github.com/ncbi/pgap.git
Path: task_types/tt_format_rrnas_from_seq_entry.cwl Branch/Commit ID: 94c97cfc95a5bf102a6f9206e045ea1afb768317 |
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1st-workflow.cwl
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https://github.com/common-workflow-language/common-workflow-language.git
Path: v1.0/examples/1st-workflow.cwl Branch/Commit ID: 25ca7e2451d290c642803ed1ad914ceed416719e |
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unifiedgenotyper.cwl
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https://github.com/uc-cdis/genomel_pipelines.git
Path: genomel/cwl/workflows/variant_calling/unifiedgenotyper.cwl Branch/Commit ID: c661469505c606e1353f23c21a6654724a9d8d63 |
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mutect parallel workflow
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/mutect.cwl Branch/Commit ID: a08de598edc04f340fdbff76c9a92336a7702022 |