Explore Workflows
View already parsed workflows here or click here to add your own
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phase VCF
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Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: 389f6edccab082d947bee9c032f59dbdf9f7c325 |
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exome alignment and germline variant detection, with optitype for HLA typing
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Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: 389f6edccab082d947bee9c032f59dbdf9f7c325 |
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RNA-Seq alignment and transcript/gene abundance workflow
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Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 389f6edccab082d947bee9c032f59dbdf9f7c325 |
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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: 389f6edccab082d947bee9c032f59dbdf9f7c325 |
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Subworkflow that runs cnvkit in single sample mode and returns a vcf file
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Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: 9e5f228bc1a3d0dfe950b5d41d7e4319e834a6d4 |
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Filter single sample sv vcf from depth callers(cnvkit/cnvnator)
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Path: definitions/subworkflows/sv_depth_caller_filter.cwl Branch/Commit ID: 9e5f228bc1a3d0dfe950b5d41d7e4319e834a6d4 |
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topmed-alignment.cwl
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Path: aligner/sbg-alignment-cwl/topmed-alignment.cwl Branch/Commit ID: de683e0be7c2798b3eb503812a095659039247b3 |
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Merge, annotate, and generate a TSV for SVs
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Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: 9e5f228bc1a3d0dfe950b5d41d7e4319e834a6d4 |
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scRNA-seq pipeline using Salmon and Alevin
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Path: pipeline.cwl Branch/Commit ID: 4db77ce1de9019ac997dd5da553ea0f11a15d9f9 |
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topmed-alignment.cwl
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Path: aligner/sbg-alignment-cwl/topmed-alignment.cwl Branch/Commit ID: 6478d5df50d7340311d18f03a056e3db97811269 |
