Explore Workflows
View already parsed workflows here or click here to add your own
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merge and annotate svs with population allele freq and vep
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Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: 195b4ab487c939eb32a55d9f78bc1befd100caae |
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trick_revsort.cwl
Reverse the lines in a document, then sort those lines. |
Path: tests/wf/trick_revsort.cwl Branch/Commit ID: 4700fbee9a5a3271eef8bc9ee595619d0720431b |
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CLE gold vcf evaluation workflow
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Path: definitions/subworkflows/vcf_eval_cle_gold.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
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taxonomy_check_16S
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Path: task_types/tt_taxonomy_check_16S.cwl Branch/Commit ID: 42712bca4c3307d87b6b55f525a4c97cb6f7e288 |
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Running cellranger count and lineage inference
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Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: 195b4ab487c939eb32a55d9f78bc1befd100caae |
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taxonomy_check_16S
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Path: task_types/tt_taxonomy_check_16S.cwl Branch/Commit ID: bc0f1f147231c759fb2d5ff99f41b2667a5588ad |
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secret_wf.cwl
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Path: tests/wf/secret_wf.cwl Branch/Commit ID: 78fe9d41ee5a44f8725dfbd7028e4a5ee42949cf |
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tt_hmmsearch_wnode.cwl
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Path: task_types/tt_hmmsearch_wnode.cwl Branch/Commit ID: bc0f1f147231c759fb2d5ff99f41b2667a5588ad |
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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: 0b6e8fd8ead7644cf5398395b76af5cf4011686f |
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sec-wf-out.cwl
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Path: tests/wf/sec-wf-out.cwl Branch/Commit ID: 78fe9d41ee5a44f8725dfbd7028e4a5ee42949cf |
