Explore Workflows
View already parsed workflows here or click here to add your own
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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: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
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kmer_cache_store
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Path: task_types/tt_kmer_cache_store.cwl Branch/Commit ID: f2bd4687f06f85ea848b6f1ce04ec97f48525334 |
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createindex.cwl
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Path: workflow/createindex.cwl Branch/Commit ID: 32d58ceccee0725981d73e1572e2f411acbb7dd8 |
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Raw sequence data to BQSR
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Path: definitions/subworkflows/sequence_to_bqsr.cwl Branch/Commit ID: 2e0562a5c3cd7aac24af4c622a5ae68a7fb23a71 |
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exome alignment and tumor-only variant detection
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Path: definitions/pipelines/tumor_only_exome.cwl Branch/Commit ID: 3b6d0475c80f5e452793a46a38ee188742b86595 |
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align_merge_sas
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Path: task_types/tt_align_merge_sas.cwl Branch/Commit ID: 1ce371c7412debef75edf09e8830d74ac987a668 |
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Unaligned BAM to BQSR
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Path: definitions/subworkflows/bam_to_bqsr.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
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varscan somatic workflow
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Path: definitions/subworkflows/varscan.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
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somatic_exome: exome alignment and somatic variant detection
somatic_exome is designed to perform processing of mutant/wildtype H.sapiens exome sequencing data. It features BQSR corrected alignments, 4 caller variant detection, and vep style annotations. Structural variants are detected via manta and cnvkit. In addition QC metrics are run, including somalier concordance metrics. example input file = analysis_workflows/example_data/somatic_exome.yaml |
Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: 174f3b239018328cec1d821947438b457552724c |
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Creates a cgf for each FastJ file
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Path: cwl-version/cgf3/createcgf-wf.cwl Branch/Commit ID: cdfe9178ad4e481d2391cd2da74b82d66a61b0bb |
