Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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scatter-wf1.cwl
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![]() Path: v1.0/v1.0/scatter-wf1.cwl Branch/Commit ID: 46947322eb5a99940eb3b5d3088e58f5189398e7 |
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umi molecular alignment workflow
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![]() Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: 767e3dc7448da5bc44e4817c4161f6e4530032e2 |
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BLAST against rRNA db
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![]() Path: bacterial_noncoding/wf_blastn.cwl Branch/Commit ID: a79cec2331b3e17e382e8e5040405e8dd750c639 |
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transform.cwl
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![]() Path: workflows/dnaseq/validate/transform.cwl Branch/Commit ID: 017c7572ea309c7d5b34bcc9bc1bdafbe47cb515 |
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sum-wf.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/sum-wf.cwl Branch/Commit ID: 216fbe57afcf67d81c99b49c1aa3aee0844f0a6a |
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running cellranger mkfastq and count
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![]() Path: definitions/subworkflows/cellranger_mkfastq_and_count.cwl Branch/Commit ID: 64e10813d527c67ed7987697d5c47cdbbaadbebd |
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haplotypecaller.cwl
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![]() Path: genomel/cwl/workflows/variant_calling/haplotypecaller.cwl Branch/Commit ID: 39ddc4b79dc93076787046f591225dc7ca3100ce |
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1st-workflow.cwl
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![]() Path: v1.0/examples/1st-workflow.cwl Branch/Commit ID: bb8d4a1231fea140a565b43a0c5b59cbde9e8c01 |
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snpeff-workflow.cwl
Annotate variants provided in a gziped VCF using SnpEff |
![]() Path: tools/snpeff-workflow.cwl Branch/Commit ID: 8607fc514b40af405b22351e1af43728f1391ea4 |
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count-lines3-wf.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/count-lines3-wf.cwl Branch/Commit ID: 691dea280b40ac177b4a38b33375139ca0ce7e81 |