Explore Workflows
View already parsed workflows here or click here to add your own
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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 |
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chipseq-header.cwl
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![]() Path: metadata/chipseq-header.cwl Branch/Commit ID: 299980af3a5cbdb4edcb27331d4846418d386e00 |
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align_sort_sa
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![]() Path: task_types/tt_align_sort_sa.cwl Branch/Commit ID: cd97086739ae5988bab09b05e9259675c4b6bce6 |
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Create a tile library (SGLF) for a given set of FastJ files
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![]() Path: cwl-version/tilelib/createsglf-wf.cwl Branch/Commit ID: cdfe9178ad4e481d2391cd2da74b82d66a61b0bb |
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Report generation workflow
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![]() Path: WGS-processing/cwl/helper/report-wf.cwl Branch/Commit ID: d147d1d1fafeeea06bd09d9479337b0f5aab43b0 |
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scatter GATK HaplotypeCaller over intervals
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![]() Path: definitions/subworkflows/gatk_haplotypecaller_iterator.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
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Varscan Workflow
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![]() Path: definitions/subworkflows/varscan_pre_and_post_processing.cwl Branch/Commit ID: 2e0562a5c3cd7aac24af4c622a5ae68a7fb23a71 |
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umi molecular alignment fastq workflow
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![]() Path: definitions/pipelines/alignment_umi_molecular.cwl Branch/Commit ID: 2e0562a5c3cd7aac24af4c622a5ae68a7fb23a71 |