Explore Workflows
View already parsed workflows here or click here to add your own
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Exome QC workflow
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Path: definitions/subworkflows/qc_exome_no_verify_bam.cwl Branch/Commit ID: 26806d99f8e2a241715fd081e712d4e3763db5b8 |
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kf_single_cell_ss2.cwl
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Path: workflows/kf_single_cell_ss2.cwl Branch/Commit ID: 8c1d2315ad46fe0a30bf618e108e55b0263c7c6d |
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conflict.cwl#main
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Path: tests/wf/conflict.cwl Branch/Commit ID: 0112ec2c4dcf5bdb2e39047ca5ac2caecaf683bf Packed ID: main |
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trim-rnaseq-se-dutp.cwl
Runs RNA-Seq dUTP BioWardrobe basic analysis with strand specific single-end data file. |
Path: workflows/trim-rnaseq-se-dutp.cwl Branch/Commit ID: cf678db8304ffaa20c1d6c854364db5ed41803c2 |
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scatter-valuefrom-wf5.cwl
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Path: cwltool/schemas/v1.0/v1.0/scatter-valuefrom-wf5.cwl Branch/Commit ID: 4bf61c8a3d519eefd8b9271af73974bec62535ba |
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main-prealign.cwl
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Path: prealign/prealign-workflow/main-prealign.cwl Branch/Commit ID: 5d37c216722d242ba09ec86e08e4bdf8a1cc690d |
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scatter-wf3.cwl#main
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Path: cwltool/schemas/v1.0/v1.0/scatter-wf3.cwl Branch/Commit ID: 4bf61c8a3d519eefd8b9271af73974bec62535ba Packed ID: main |
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scatter-valuefrom-wf5.cwl
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Path: cwltool/schemas/v1.0/v1.0/scatter-valuefrom-wf5.cwl Branch/Commit ID: 17268d1493d9e558113b2c35c0be6b3fb961b2a3 |
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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 |
