Explore Workflows
View already parsed workflows here or click here to add your own
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abra_workflow.cwl
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![]() Path: workflows/ABRA/abra_workflow.cwl Branch/Commit ID: 5bf88423593441e4bf6b432111160446cd8dcf13 |
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bqsr_workflow.cwl
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![]() Path: workflows/BQSR/bqsr_workflow.cwl Branch/Commit ID: 5bf88423593441e4bf6b432111160446cd8dcf13 |
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extract_readgroup_fastq_se.cwl
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![]() Path: workflows/bamfastq_align/extract_readgroup_fastq_se.cwl Branch/Commit ID: 6b43e8b03256492f2b36ffcf548704daaafee6f6 |
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xenbase-sra-to-fastq-se.cwl
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![]() Path: subworkflows/xenbase-sra-to-fastq-se.cwl Branch/Commit ID: afbec98437a7796a509fffbad8c3370aa099f059 |
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count-lines9-wf.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/count-lines9-wf.cwl Branch/Commit ID: 203797516329f7fb8aa5e763e6f9b331c63c3060 |
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secret_wf.cwl
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![]() Path: tests/wf/secret_wf.cwl Branch/Commit ID: e62a8406b448220969ee172699f61c5ca379d60c |
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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: 457e101e3fb87e7fd792357afce00ed8ccbfbcdb |
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exome alignment and germline variant detection, with optitype for HLA typing
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![]() Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: 457e101e3fb87e7fd792357afce00ed8ccbfbcdb |
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Tumor-Only Detect Variants workflow
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![]() Path: definitions/pipelines/tumor_only_detect_variants.cwl Branch/Commit ID: 449bc7e45bb02316d040f73838ef18359e770268 |
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exome alignment with qc
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![]() Path: definitions/pipelines/alignment_exome.cwl Branch/Commit ID: 00df82a529a58d362158110581e1daa28b4d7ecb |