Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and germline variant detection
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Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: 049f4aeff4c4a1b8421cac9b1c1c1f0da5848315 |
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Per-region pindel
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Path: definitions/subworkflows/pindel_cat.cwl Branch/Commit ID: 889a077a20c0fdb01f4ed97aa4bc40f920c37a1a |
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exome alignment and germline variant detection
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Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: 1560e7817fdb71d58aca7f98aba68809d840ade1 |
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kmer_ref_compare_wnode
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Path: task_types/tt_kmer_ref_compare_wnode.cwl Branch/Commit ID: a34f47d1e37af51e387ecdfa5c3047f106c1146b |
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Detect Variants workflow for WGS pipeline
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Path: definitions/pipelines/detect_variants_wgs.cwl Branch/Commit ID: b465f0da2806ddb6df481409541d13288ccb40ec |
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gathered exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/somatic_exome_cle_gathered.cwl Branch/Commit ID: 789267ce0e3fed674ea5212a562315218fcf1bfc |
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haplotypecaller.cwl
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Path: per-sample/Workflows/haplotypecaller.cwl Branch/Commit ID: 651b97b982a48cdb4e5f36edc0b1f38b25b30c10 |
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kmer_build_tree
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Path: task_types/tt_kmer_build_tree.cwl Branch/Commit ID: 146df33e2e44afa2a608ac72c036e6b6b871af93 |
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consensus_maf.cwl
Workflow to merge a large number of maf files into a single consensus maf file for use with GetBaseCountsMultiSample |
Path: cwl/consensus_maf.cwl Branch/Commit ID: 9f7b5b5f985727a2df34ae86586c296ce757004c |
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varscan somatic workflow
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Path: definitions/subworkflows/varscan.cwl Branch/Commit ID: ec45fad68ca10fb64d5c58e704991b146dc31d28 |
