Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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manyjobs.cwl
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![]() Path: manyjobs/manyjobs.cwl Branch/Commit ID: main |
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WGS QC workflow
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![]() Path: definitions/subworkflows/qc_wgs.cwl Branch/Commit ID: d297528e53b6c1ecb69b1ab27b8e03323b4463ad |
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chromVAR scATAC-seq pipeline
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![]() Path: chromvar-pipeline.cwl Branch/Commit ID: master |
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sidearm.cwl
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![]() Path: cwl/tools/sidearm.cwl Branch/Commit ID: master |
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workflow.cwl
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![]() Path: bioinformatics/tools/workflow.cwl Branch/Commit ID: master |
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tld.cwl
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![]() Path: tools/cwlprov_to_crate/tld/tld.cwl Branch/Commit ID: tld_workflow_bad_connection |
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functional analysis prediction with InterProScan
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![]() Path: workflows/functional_analysis.cwl Branch/Commit ID: master |
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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: master |
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Exome QC workflow
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![]() Path: qc/workflow_exome.cwl Branch/Commit ID: master |
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Filter single sample sv vcf from paired read callers(Manta/Smoove)
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![]() Path: definitions/subworkflows/sv_paired_read_caller_filter.cwl Branch/Commit ID: downsample_and_recall |