Explore Workflows
View already parsed workflows here or click here to add your own
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FASTQ to BQSR
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Path: definitions/subworkflows/fastq_to_bqsr.cwl Branch/Commit ID: 0b0ad1a54f0f6849dc645449b079470448a23095 |
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cond-wf-002.cwl
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Path: tests/conditionals/cond-wf-002.cwl Branch/Commit ID: b60a42e3cc417c5b75b88fd7c6681abcc7ff5b89 |
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umi molecular alignment workflow
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Path: definitions/subworkflows/molecular_qc.cwl Branch/Commit ID: f7ac3eff79128831c9f7a565d5b187882f39aa58 |
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alignment_novoalign.cwl
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Path: genomel/cwl/workflows/harmonization/alignment_novoalign.cwl Branch/Commit ID: 301eb97ef0e0970b04ad1a91e460db2b210b6886 |
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Unaligned BAM to BQSR and VCF
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Path: definitions/subworkflows/bam_to_bqsr.cwl Branch/Commit ID: 3c7a6e39d956ca065751f23ee0316ac3f3306d9a |
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count-lines19-wf.cwl
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Path: tests/count-lines19-wf.cwl Branch/Commit ID: 979083396fee912fca8ef778174216d317338a00 |
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heatmap-prepare.cwl
Workflow runs homer-make-tag-directory.cwl tool using scatter for the following inputs - bam_file - fragment_size - total_reads `dotproduct` is used as a `scatterMethod`, so one element will be taken from each array to construct each job: 1) bam_file[0] fragment_size[0] total_reads[0] 2) bam_file[1] fragment_size[1] total_reads[1] ... N) bam_file[N] fragment_size[N] total_reads[N] `bam_file`, `fragment_size` and `total_reads` arrays should have the identical order. |
Path: tools/heatmap-prepare.cwl Branch/Commit ID: 30e58892852641802b37912608fafbd8dc98918a |
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record-output-wf_v1_2.cwl
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Path: testdata/record-output-wf_v1_2.cwl Branch/Commit ID: 6a46105708870aa3cf97c8ba91884272b2857975 |
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count-lines8-wf-noET.cwl
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Path: tests/count-lines8-wf-noET.cwl Branch/Commit ID: 7d7986a6e852ca6e3239c96d3a05dd536c76c903 |
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starfishRunner.cwl
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Path: steps/starfishRunner.cwl Branch/Commit ID: 6ef7a6399b2ab55c1d3edd4e37631a8234889fd9 |
