Explore Workflows
View already parsed workflows here or click here to add your own
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gatk4_cohort_genotyping.cwl
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Path: genomel/cwl/workflows/variant_calling/gatk4_cohort_genotyping.cwl Branch/Commit ID: 13c106834d6c9031de08496faeff521740a0c95f |
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Varscan Workflow
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Path: definitions/subworkflows/varscan_pre_and_post_processing.cwl Branch/Commit ID: 889a077a20c0fdb01f4ed97aa4bc40f920c37a1a |
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strelka workflow
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Path: definitions/subworkflows/strelka_and_post_processing.cwl Branch/Commit ID: 889a077a20c0fdb01f4ed97aa4bc40f920c37a1a |
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Apply filters to VCF file
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Path: definitions/subworkflows/filter_vcf_nonhuman.cwl Branch/Commit ID: 889a077a20c0fdb01f4ed97aa4bc40f920c37a1a |
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Bisulfite QC tools
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Path: definitions/subworkflows/bisulfite_qc.cwl Branch/Commit ID: 889a077a20c0fdb01f4ed97aa4bc40f920c37a1a |
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bam to trimmed fastqs and biscuit alignments
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Path: definitions/subworkflows/bam_to_trimmed_fastq_and_biscuit_alignments.cwl Branch/Commit ID: 889a077a20c0fdb01f4ed97aa4bc40f920c37a1a |
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Tumor-Only Detect Variants workflow
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Path: definitions/pipelines/tumor_only_detect_variants.cwl Branch/Commit ID: 889a077a20c0fdb01f4ed97aa4bc40f920c37a1a |
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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: 889a077a20c0fdb01f4ed97aa4bc40f920c37a1a |
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Detect Variants workflow
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Path: definitions/pipelines/detect_variants.cwl Branch/Commit ID: 1249b5d4e23d57ca5e3b8ad6d8e5f10ddb019f68 |
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mutect parallel workflow
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Path: definitions/subworkflows/mutect.cwl Branch/Commit ID: 049f4aeff4c4a1b8421cac9b1c1c1f0da5848315 |
