Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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workflow.cwl
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![]() Path: flow_dispatch/workflow.cwl Branch/Commit ID: 6f0888f9e4b15172109dcb1db2ee63f154a79100 |
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Bacterial Annotation, pass 4, blastp-based functional annotation (second pass)
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![]() Path: bacterial_annot/wf_bacterial_annot_pass4.cwl Branch/Commit ID: dev |
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canine_annotation_module.cwl
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![]() Path: subworkflows/canine_annotation_module.cwl Branch/Commit ID: master |
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cnv_exomedepth
CNV ExomeDepth calling |
![]() Path: structuralvariants/cwl/subworkflows/cnv_exome_depth.cwl Branch/Commit ID: 1.0.9 |
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epigenome-chip-seq.cwl
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![]() Path: workflow/epigenome-chip-seq/epigenome-chip-seq.cwl Branch/Commit ID: main |
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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: low-vaf |
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wf-loadContents2.cwl
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![]() Path: tests/wf-loadContents2.cwl Branch/Commit ID: main |
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Gathered Downsample and HaplotypeCaller
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![]() Path: definitions/pipelines/gathered_downsample_and_recall.cwl Branch/Commit ID: master |
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Transcriptome assembly workflow (paired-end version)
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![]() Path: workflows/TranscriptomeAssembly-wf.paired-end.cwl Branch/Commit ID: assembly |
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SSU-from-tablehits.cwl
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![]() Path: tools/SSU-from-tablehits.cwl Branch/Commit ID: master |