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trim-rnaseq-pe.cwl
Runs RNA-Seq BioWardrobe basic analysis with pair-end data file. |
Path: workflows/trim-rnaseq-pe.cwl Branch/Commit ID: 4723ce567089dc9ee51e067b813c5b527a3da16a |
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tt_kmer_top_n.cwl
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Path: task_types/tt_kmer_top_n.cwl Branch/Commit ID: 8761d0526f932dea879403d51251316ef331f082 |
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workflow.cwl
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Path: flow_download/workflow.cwl Branch/Commit ID: 6f0888f9e4b15172109dcb1db2ee63f154a79100 |
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gaps_or_not.cwl
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Path: gaps_or_not.cwl Branch/Commit ID: 6f0888f9e4b15172109dcb1db2ee63f154a79100 |
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env-wf1.cwl
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Path: cwltool/schemas/v1.0/v1.0/env-wf1.cwl Branch/Commit ID: 17268d1493d9e558113b2c35c0be6b3fb961b2a3 |
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count-lines12-wf.cwl
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Path: tests/count-lines12-wf.cwl Branch/Commit ID: 5e3fac092a720c5670ae3e787eabe1aaade71d83 |
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ani_top_n
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Path: task_types/tt_ani_top_n.cwl Branch/Commit ID: e4d6182d5f7a6a880e5f2b21273cf40d25e187df |
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Chipseq alignment with qc and creating homer tag directory
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Path: definitions/pipelines/chipseq_alignment.cwl Branch/Commit ID: 4ae14dd3a447c90022e3dfeb53fc05b8436e2775 |
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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: 4723ce567089dc9ee51e067b813c5b527a3da16a |
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scatter-wf4.cwl#main
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Path: tests/wf/scatter-wf4.cwl Branch/Commit ID: 048eb55aefd8d71d161fbc89ec0e888b8bfa0aa1 Packed ID: main |
