Explore Workflows
View already parsed workflows here or click here to add your own
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wgs alignment and germline variant detection
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Path: definitions/pipelines/germline_wgs.cwl Branch/Commit ID: 9a657bc8c462542dc7f57fba9e04dc1669f966ba |
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mut3.cwl
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Path: tests/wf/mut3.cwl Branch/Commit ID: c6cced7a2e6389d2eb43342e702677ccb7c7497c |
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mut2.cwl
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Path: tests/wf/mut2.cwl Branch/Commit ID: 6003cbb94f16103241b562f2133e7c4acac6c621 |
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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: 7ced5a5259dbd8b3fc64456beaeffd44f4a24081 |
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ChIP-seq peak caller workflow MACS2 based
This workflow execute peak caller and QC for ChIP-seq using MACS2 |
Path: workflows/ChIP-Seq/peak-calling-MACS2.cwl Branch/Commit ID: dde32ff6c8e653a4e6b93316f28737706d5ec367 |
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umi molecular alignment workflow
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Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: 86fbeb95ef85111f3b4c6bc2bba8f06cef64e157 |
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exome alignment and germline variant detection
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Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: 8c4e7372247a7f4ed9ed478ef8ea1d239bc88af0 |
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trim-rnaseq-pe.cwl
Runs RNA-Seq BioWardrobe basic analysis with pair-end data file. |
Path: workflows/trim-rnaseq-pe.cwl Branch/Commit ID: cb5e5b8563be4977e9f2babc14fe084faa234847 |
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harmonization_novoalign_multi_readgroup.cwl
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Path: genomel/cwl/workflows/harmonization/harmonization_novoalign_multi_readgroup.cwl Branch/Commit ID: 91e222adeeee0bd567a5bf2385400610fad0d3a9 |
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Subworkflow to allow calling cnvkit with cram instead of bam files
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Path: definitions/subworkflows/cram_to_cnvkit.cwl Branch/Commit ID: bcc6adaf15035f5ce6fc851e27b1173b0fd20c1c |
