Explore Workflows
View already parsed workflows here or click here to add your own
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Subworkflow to allow calling different SV callers which require bam files as inputs
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Path: definitions/subworkflows/single_sample_sv_callers.cwl Branch/Commit ID: ffab5424bb8b5905aecf6f8e2e6387da7f3df562 |
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WGS QC workflow
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Path: definitions/subworkflows/qc_wgs.cwl Branch/Commit ID: 3ee63d8757c341ca98b3b46ec4782862ad19b710 |
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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: 5be54bf09092c53e6c7797a875f64a360d511d7f |
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exome alignment with qc
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Path: definitions/pipelines/exome_alignment.cwl Branch/Commit ID: aba52e94b6d7470132d3c092c26d67e29d615300 |
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transcriptome_cleanup
This workflow detect and remove vector, duplicate and contamination from a transcriptome fasta file |
Path: workflows/Annotation/transcriptome-cleanup.cwl Branch/Commit ID: e6efd0c93582ad6435ed10020544ef8982a25a8e |
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count-lines1-wf-noET.cwl
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Path: tests/count-lines1-wf-noET.cwl Branch/Commit ID: c7c97715b400ff2194aa29fc211d3401cea3a9bf |
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Detect Variants workflow
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Path: definitions/pipelines/detect_variants.cwl Branch/Commit ID: aba52e94b6d7470132d3c092c26d67e29d615300 |
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Apply filters to VCF file
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Path: definitions/subworkflows/filter_vcf_mouse.cwl Branch/Commit ID: 24e5290aec441665c6976ee3ee8ae3574c49c6b5 |
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wffail.cwl
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Path: tests/wf/wffail.cwl Branch/Commit ID: 31aa094dce60cbb176229d6b918bfd5ae09c0390 |
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Subworkflow to allow calling cnvkit with cram instead of bam files
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Path: definitions/subworkflows/cram_to_cnvkit.cwl Branch/Commit ID: 3ee63d8757c341ca98b3b46ec4782862ad19b710 |
