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: cwl/workflow.cwl Branch/Commit ID: pack_test |
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sec-wf.cwl
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![]() Path: tests/wf/sec-wf.cwl Branch/Commit ID: main |
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workflow1_11.cwl#UncompressDatatables.cwl
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![]() Path: workflow1_11.cwl Branch/Commit ID: main Packed ID: UncompressDatatables.cwl |
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cgpRna_workflow.cwl
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![]() Path: cwls/cgpRna_workflow.cwl Branch/Commit ID: ad389b843b2944245f5442b65fb3c684829b8c5d |
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host.sort.workflow.cwl
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![]() Path: cwl/host.sort.workflow.cwl Branch/Commit ID: master |
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collate_unique_SSU_headers.cwl
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![]() Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: fa86fce |
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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: downsample_and_recall |
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LodSeq
LodSeq performs the genetic linkage analysis across families, by computing lod-scores given a gvcf file and a related tfam pedigree file. |
![]() Path: workflows/cwltoil/lodseq.cwl Branch/Commit ID: master |
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md5sum-workflow.cwl
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![]() Path: md5sum/md5sum-workflow.cwl Branch/Commit ID: master |
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chksum_for_corrupted_files.cwl
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![]() Path: cwls/chksum_for_corrupted_files.cwl Branch/Commit ID: 0.5.0_test |