Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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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: 92bdcd9fa879161834ecdb1c4c9ac7c46e940206 |
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exome alignment and germline variant detection, with optitype for HLA typing
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![]() Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: adcae308fdccaa1190083616118dfadb4df65dca |
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exome alignment and tumor-only variant detection
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![]() Path: definitions/pipelines/exome.cwl Branch/Commit ID: 7f9dfad8e45ca096ae738cff646195b2b1ba7d7f |
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scatter-wf4.cwl#main
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![]() Path: tests/wf/scatter-wf4.cwl Branch/Commit ID: 9e7c68c0834645ba53a7e2b5f70d53df9d051c92 Packed ID: main |
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scatter-valuefrom-inputs-wf1.cwl
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![]() Path: tests/scatter-valuefrom-inputs-wf1.cwl Branch/Commit ID: ad91c844b5adfef514c059af364e20afc935e598 |
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hello_world_checker.cwl
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![]() Path: hello_world_checker.cwl Branch/Commit ID: f6f58673d4818857d069f2e44f0a6e2fe8ba1e64 |
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SoupX (workflow) - an R package for the estimation and removal of cell free mRNA contamination
Wrapped in a workflow SoupX tool for easy access to Cell Ranger pipeline compressed outputs. |
![]() Path: tools/soupx-subworkflow.cwl Branch/Commit ID: cf678db8304ffaa20c1d6c854364db5ed41803c2 |
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count-lines9-wf.cwl
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![]() Path: tests/count-lines9-wf.cwl Branch/Commit ID: ad91c844b5adfef514c059af364e20afc935e598 |
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step-valuefrom2-wf.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/step-valuefrom2-wf.cwl Branch/Commit ID: b3639a4c5075abc562b7f9b816be0d4f7d711703 |
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js_output_workflow.cwl
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![]() Path: tests/wf/js_output_workflow.cwl Branch/Commit ID: 1338ffbf2492a2ca1be1d7c5c46597bd9205aa24 |