Explore Workflows
View already parsed workflows here or click here to add your own
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Detect Variants workflow
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Path: definitions/pipelines/detect_variants_mouse.cwl Branch/Commit ID: efbbe5ed51f6ac583e87a348785c72818a33f56e |
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step-valuefrom2-wf_v1_2.cwl
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Path: testdata/step-valuefrom2-wf_v1_2.cwl Branch/Commit ID: 15c8467d6d3c31a95ccc682095cf34aad125ca8c |
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conflict.cwl#main
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Path: tests/wf/conflict.cwl Branch/Commit ID: 0cbbd92a87b1ba1d484bf50170c2749536fbbe77 Packed ID: main |
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workflow_input_sf_expr_v1_1.cwl
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Path: testdata/workflow_input_sf_expr_v1_1.cwl Branch/Commit ID: 02d6dbd3d48d50adfd4afb1f7d92e8a4284bcab9 |
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scatter-wf4.cwl#main
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Path: tests/wf/scatter-wf4.cwl Branch/Commit ID: 2c48ccc9c67e4d5671ec32d2182d25d7a0bb631d Packed ID: main |
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trim-chipseq-se.cwl
Runs ChIP-Seq BioWardrobe basic analysis with single-end data file. |
Path: workflows/trim-chipseq-se.cwl Branch/Commit ID: 9a03dbe8829ca649814d9c8bd11fe3a673750a95 |
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tt_kmer_top_n.cwl
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Path: task_types/tt_kmer_top_n.cwl Branch/Commit ID: 205f4ceb47ba7537a6923d2dfb03668317c2fd89 |
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Whole genome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_wgs.cwl Branch/Commit ID: c6bbd4cdd612b3b5cc6e9000df4800c21e192bf5 |
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process-ddf.cwl
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Path: workflows/process-ddf.cwl Branch/Commit ID: d77bb56f954217d3ba2aae801f1a08470b0793df |
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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: 026bba9511561246ad65458f0f55c88cead26fbd |
