Explore Workflows
View already parsed workflows here or click here to add your own
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Exome QC workflow
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Path: definitions/subworkflows/qc_exome.cwl Branch/Commit ID: f90b39e1b05e9bb37079b09f337f7e7ba5027f99 |
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Per-chromosome pindel
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Path: definitions/subworkflows/pindel_cat.cwl Branch/Commit ID: 88f1e02b261bf9ce882eba306b6245c64328632b |
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umi molecular alignment workflow
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Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: f90b39e1b05e9bb37079b09f337f7e7ba5027f99 |
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exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/somatic_exome_cle.cwl Branch/Commit ID: c6bbd4cdd612b3b5cc6e9000df4800c21e192bf5 |
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exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/cle_somatic_exome.cwl Branch/Commit ID: 479c9b3e3fa32ec9c7cd4073cfbccc675fd254d9 |
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alignment for nonhuman with qc
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Path: definitions/pipelines/alignment_wgs_nonhuman.cwl Branch/Commit ID: b465f0da2806ddb6df481409541d13288ccb40ec |
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count-lines11-wf.cwl
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Path: cwltool/schemas/v1.0/v1.0/count-lines11-wf.cwl Branch/Commit ID: a0f7d43bbc706af2a844be93fc19b2e4e4da626c |
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trim-rnaseq-pe-dutp.cwl
Runs RNA-Seq BioWardrobe basic analysis with strand specific pair-end data file. |
Path: workflows/trim-rnaseq-pe-dutp.cwl Branch/Commit ID: 14d0618786c1499e8626f234341e99782a1e55c2 |
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Subworkflow that runs cnvkit in single sample mode and returns a vcf file
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Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: f90b39e1b05e9bb37079b09f337f7e7ba5027f99 |
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Bisulfite QC tools
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Path: definitions/subworkflows/bisulfite_qc.cwl Branch/Commit ID: 1585504ccffafac53b1594349ed934f45206ee2b |
