Explore Workflows
View already parsed workflows here or click here to add your own
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VIRTUS.SE.singlevirus.cwl
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Path: workflow/VIRTUS.SE.singlevirus.cwl Branch/Commit ID: 49faf55f97c8f3084b426d2db6640519d6f2ce71 |
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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: 93656ed6582073e434eab168c610625a835dce37 |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 93656ed6582073e434eab168c610625a835dce37 |
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Run genomic CMsearch
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Path: bacterial_noncoding/wf_gcmsearch.cwl Branch/Commit ID: 681555881cbdf95a1f4c29f6dc272eb6ca8e4d60 |
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iwdr-passthrough-successive.cwl
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Path: tests/wf/iwdr-passthrough-successive.cwl Branch/Commit ID: 0cbbd92a87b1ba1d484bf50170c2749536fbbe77 |
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mut.cwl
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Path: tests/wf/mut.cwl Branch/Commit ID: 22bc7d80dd524767b7d7d115747556ac62c27e9f |
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Running cellranger count and lineage inference
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Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: d57c2af01a3cb6016e5a264f60641eafd2e5aa05 |
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exome alignment with qc
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Path: definitions/pipelines/exome_alignment.cwl Branch/Commit ID: d297528e53b6c1ecb69b1ab27b8e03323b4463ad |
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1st-workflow.cwl
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Path: tests/wf/1st-workflow.cwl Branch/Commit ID: baefdcb58fcc76e3378cf705fc6a3e69ef35bb47 |
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merge_svs.cwl
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Path: wdl2cwl/tests/cwl_files/merge_svs.cwl Branch/Commit ID: e910788d1f62bf470cc71f19af0713b79893f4ee |
