Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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echo-wc_inline.cwl
Counts words of a message via echo and wc |
![]() Path: tests/data/workflows/echo-wc_inline.cwl Branch/Commit ID: master |
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joint genotyping for trios or small cohorts
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![]() Path: definitions/subworkflows/joint_genotype.cwl Branch/Commit ID: master |
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SPRM pipeline
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![]() Path: pipeline.cwl Branch/Commit ID: d2d5127 |
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running cellranger mkfastq and count
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![]() Path: definitions/subworkflows/cellranger_mkfastq_and_count.cwl Branch/Commit ID: low-vaf |
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waltz-workflow.cwl
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![]() Path: workflows/waltz/waltz-workflow.cwl Branch/Commit ID: master |
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io-int-wf.cwl
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![]() Path: tests/io-int-wf.cwl Branch/Commit ID: main |
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kfdrc_RNAseq_workflow.cwl
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![]() Path: workflow/kfdrc_RNAseq_workflow.cwl Branch/Commit ID: master |
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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: low-vaf |
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adapter for sequence_align_and_tag
Some workflow engines won't stage files in our nested structure, so parse it out here |
![]() Path: definitions/subworkflows/sequence_align_and_tag_adapter.cwl Branch/Commit ID: master |
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Exome QC workflow
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![]() Path: definitions/subworkflows/qc_exome.cwl Branch/Commit ID: master |