Explore Workflows
View already parsed workflows here or click here to add your own
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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: dc2c019c1aa24cc01b451a0f048cf94a35f163c4 |
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Build STAR indices
Workflow runs [STAR](https://github.com/alexdobin/STAR) v2.5.3a (03/17/2017) PMID: [23104886](https://www.ncbi.nlm.nih.gov/pubmed/23104886) to build indices for reference genome provided in a single FASTA file as fasta_file input and GTF annotation file from annotation_gtf_file input. Generated indices are saved in a folder with the name that corresponds to the input genome. |
Path: workflows/star-index.cwl Branch/Commit ID: fa4f172486288a1a9d23864f1d6962d85a453e16 |
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cond-wf-012.cwl
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Path: tests/conditionals/cond-wf-012.cwl Branch/Commit ID: 7d7986a6e852ca6e3239c96d3a05dd536c76c903 |
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Pairwise genomic regions intersection
Pairwise genomic regions intersection ============================================= Overlaps peaks from two ChIP/ATAC experiments |
Path: workflows/peak-intersect.cwl Branch/Commit ID: fa4f172486288a1a9d23864f1d6962d85a453e16 |
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scatterfail.cwl
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Path: tests/wf/scatterfail.cwl Branch/Commit ID: 4bb5329997cb84562a40733b5c2f55600b1a741a |
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record-in-secondaryFiles-missing-wf.cwl
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Path: tests/record-in-secondaryFiles-missing-wf.cwl Branch/Commit ID: 3e90671b25f7840ef2926ad2bacbf447772dda94 |
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lane_map_and_stats.cwl
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Path: cwls/tools/lane_map_and_stats.cwl Branch/Commit ID: 6d77a181dc077de726bc78a19d30c22399797312 |
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phase VCF
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Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: 8cee1920920ed73384fb3ab74272da9c92a20cf2 |
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count-lines9-wf-noET.cwl
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Path: tests/count-lines9-wf-noET.cwl Branch/Commit ID: 7d7986a6e852ca6e3239c96d3a05dd536c76c903 |
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umi molecular alignment workflow
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Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: d2c2f2eb846ae2e9cdcab46e3bb88e42126cb3f5 |
