Explore Workflows
View already parsed workflows here or click here to add your own
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Non-Coding Bacterial Genes
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![]() Path: bacterial_noncoding/wf_bacterial_noncoding.cwl Branch/Commit ID: 54c5074587af001a44eccb4762a4cb25fa24cb3e |
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Varscan Workflow
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![]() Path: definitions/subworkflows/varscan_germline.cwl Branch/Commit ID: 86fbeb95ef85111f3b4c6bc2bba8f06cef64e157 |
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Nested workflow example
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![]() Path: tests/wf/nested.cwl Branch/Commit ID: 5ef2516220cd2ed327ba7966e7d812de969f4eea |
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Whole genome alignment and somatic variant detection
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![]() Path: definitions/pipelines/somatic_wgs.cwl Branch/Commit ID: 8c4e7372247a7f4ed9ed478ef8ea1d239bc88af0 |
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mut2.cwl
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![]() Path: tests/wf/mut2.cwl Branch/Commit ID: ecdfe1ee769d05790f70ac87a711131f441f3753 |
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tt_kmer_compare_wnode
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![]() Path: task_types/tt_kmer_compare_wnode.cwl Branch/Commit ID: be5ae41801b19ebc69a2889d8fdb39e8e2359611 |
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Subworkflow to allow calling cnvkit with cram instead of bam files
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![]() Path: definitions/subworkflows/cram_to_cnvkit.cwl Branch/Commit ID: 49508a2757ff2f49f1c200774a38af1c12b531bf |
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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: 2caa50434966ebdf4b33e5ca689c2e4df32f9058 |
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Run genomic CMsearch (Rfam rRNA)
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![]() Path: bacterial_ncrna/wf_gcmsearch.cwl Branch/Commit ID: 54c5074587af001a44eccb4762a4cb25fa24cb3e |
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bam to trimmed fastqs and biscuit alignments
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![]() Path: definitions/subworkflows/bam_to_trimmed_fastq_and_biscuit_alignments.cwl Branch/Commit ID: 040a3d1a719736d7fce6db83702d3fb7f9d69eac |