Explore Workflows
View already parsed workflows here or click here to add your own
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scatter2.cwl
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Path: tests/wf/scatter2.cwl Branch/Commit ID: dbc4c4c2ad30ed31367b4fbcc3bb4084fdcabaa2 |
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kmer_ref_compare_wnode
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Path: task_types/tt_kmer_ref_compare_wnode.cwl Branch/Commit ID: a7fced3ed8c839272c8f3a8db9da7bc8cd50271f |
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SoupX (workflow) - an R package for the estimation and removal of cell free mRNA contamination
Wrapped in a workflow SoupX tool for easy access to Cell Ranger pipeline compressed outputs. |
Path: tools/soupx-subworkflow.cwl Branch/Commit ID: 69643d8c15f5357a320aa7e2f6adb2e71302fd20 |
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SoupX Estimate
SoupX Estimate ============== |
Path: workflows/soupx.cwl Branch/Commit ID: 69643d8c15f5357a320aa7e2f6adb2e71302fd20 |
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Apply filters to VCF file
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Path: definitions/subworkflows/filter_vcf.cwl Branch/Commit ID: b7d9ace34664d3cedb16f2512c8a6dc6debfc8ca |
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gatk-4.0.0.0-joint-calling.cwl
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Path: cwl/workflows/gatk-4.0.0.0-joint-calling.cwl Branch/Commit ID: 95babe5d8779c036e3499940544c7709600929d1 |
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scatter-valuefrom-wf5.cwl
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Path: cwltool/schemas/v1.0/v1.0/scatter-valuefrom-wf5.cwl Branch/Commit ID: 7ec307b01442936fad9b1149f4500496557505ff |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: f42c889734c8f709ad2fd9090493bcaac8326c98 |
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Detect DoCM variants
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Path: definitions/subworkflows/docm_germline.cwl Branch/Commit ID: da335d9963418f7bedd84cb2791a0df1b3165ffe |
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allele-vcf-rnaseq-pe.cwl
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Path: workflows/allele-vcf-rnaseq-pe.cwl Branch/Commit ID: ca2dbb71d0537b1d93a8bd44719250cf8949b157 |
