Explore Workflows
View already parsed workflows here or click here to add your own
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umi molecular alignment workflow
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Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: 0b0ad1a54f0f6849dc645449b079470448a23095 |
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wgs alignment with qc
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Path: definitions/pipelines/alignment_wgs.cwl Branch/Commit ID: f42c889734c8f709ad2fd9090493bcaac8326c98 |
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Detect Variants workflow for WGS pipeline
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Path: definitions/pipelines/detect_variants_wgs.cwl Branch/Commit ID: f42c889734c8f709ad2fd9090493bcaac8326c98 |
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scatterfail.cwl
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Path: tests/wf/scatterfail.cwl Branch/Commit ID: 63f539ba60e91f0cb3ce7cda2c5da5c65525c375 |
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bgzip and index VCF
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Path: definitions/subworkflows/bgzip_and_index.cwl Branch/Commit ID: 60d8a9e6c5f571ec9b37f10290a1f4613013f3e1 |
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fp_filter workflow
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Path: definitions/subworkflows/fp_filter.cwl Branch/Commit ID: 60d8a9e6c5f571ec9b37f10290a1f4613013f3e1 |
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varscan somatic workflow
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Path: definitions/subworkflows/varscan.cwl Branch/Commit ID: 60d8a9e6c5f571ec9b37f10290a1f4613013f3e1 |
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contaminant_cleanup
This workflow detect and remove contamination from a DNA fasta file |
Path: workflows/Contamination/contaminant-cleanup.cwl Branch/Commit ID: b5a440939ac6022ee81aeeb0dd7daf3983228a61 |
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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: d57c2af01a3cb6016e5a264f60641eafd2e5aa05 |
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cram-get-fasta.cwl
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Path: cwl/workflows/cram-get-fasta.cwl Branch/Commit ID: 4a92da8c82787588863e223c431d921801049f91 |
