Explore Workflows
View already parsed workflows here or click here to add your own
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phase VCF
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Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: 6bfb64375e7ebb6eb40f463ede86d8deccdb9eff |
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scatter-wf4.cwl#main
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Path: tests/wf/scatter-wf4.cwl Branch/Commit ID: 256306a5da1eb0a8391d5f6734e7baae96922079 Packed ID: main |
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rnaseq-alignment-quantification-nosplice
This workflow QC, alignment and quantification from TPMCalculator for not spliced genomes |
Path: workflows/RNA-Seq/rnaseq-alignment-quantification_nosplice.cwl Branch/Commit ID: 793e327acc1d159ff601043ee88651fca62350dd |
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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: 0d2f354af9192a56af258a7d2426c7c160f4ec1a |
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mut.cwl
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Path: tests/wf/mut.cwl Branch/Commit ID: cd1ba3df3745fba4b635f05c67ebeaf3b8a9f4ec |
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Nested workflow example
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Path: tests/wf/double-nested.cwl Branch/Commit ID: 1338ffbf2492a2ca1be1d7c5c46597bd9205aa24 |
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scatter-valuefrom-wf4.cwl#main
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Path: cwltool/schemas/v1.0/v1.0/scatter-valuefrom-wf4.cwl Branch/Commit ID: 2256a30d0c1365b30e0a7338fb883c74674fcd25 Packed ID: main |
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harmonization_novoalign.cwl
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Path: genomel/cwl/workflows/harmonization/harmonization_novoalign.cwl Branch/Commit ID: 342c8a39d5823bbcf298d2f807ec235910e5f412 |
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env-wf1.cwl
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Path: cwltool/schemas/v1.0/v1.0/env-wf1.cwl Branch/Commit ID: 31aa094dce60cbb176229d6b918bfd5ae09c0390 |
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count-lines4-wf.cwl
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Path: cwltool/schemas/v1.0/v1.0/count-lines4-wf.cwl Branch/Commit ID: 31aa094dce60cbb176229d6b918bfd5ae09c0390 |
