Explore Workflows
View already parsed workflows here or click here to add your own
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md5sum_v12.cwl
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![]() Path: testdata/md5sum_v12.cwl Branch/Commit ID: b926e330eba795f3acc1f71fd0645e75f925a2da |
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scatter-wf4.cwl#main
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![]() Path: tests/wf/scatter-wf4.cwl Branch/Commit ID: d64178072bc4fc9700ab80cdf90146890b96587e Packed ID: main |
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example.cwl
Example CWL workflow that uses some advanced features |
![]() Path: cwl/example.cwl Branch/Commit ID: dbff0c5ae06a8b21ec70bc8279f32bce151cbfc2 |
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bacterial_screening.cwl
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![]() Path: vecscreen/bacterial_screening.cwl Branch/Commit ID: a1f39f21670be28427ceb91ceaeb9339545c18fc |
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joint genotyping for trios or small cohorts
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![]() Path: definitions/subworkflows/joint_genotype.cwl Branch/Commit ID: 31a179d7a2f2ac86bfd7fcc4dc79832c3739ae76 |
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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: 480c438a6a7e78c624712aec01bc4214d2bc179c |
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Detect Variants workflow
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![]() Path: definitions/pipelines/detect_variants_mouse.cwl Branch/Commit ID: 4ae14dd3a447c90022e3dfeb53fc05b8436e2775 |
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annotate.cwl
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![]() Path: steps/annotate.cwl Branch/Commit ID: 092373445cddc0799ce3ba15c9b609e2df86552f |
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Dockstore.cwl
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![]() Path: Dockstore.cwl Branch/Commit ID: 2ba9f641ee82d93f19c3e5e04b3bbdea5de406b3 |
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predictions.cwl
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![]() Path: docs/examples/draft/ml-predict-pipeline-streamflow/predictions.cwl Branch/Commit ID: ac8a829144ad496c08fc3b0eb41cd64848c41582 |