Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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tt_fscr_calls_pass1
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![]() Path: task_types/tt_fscr_calls_pass1.cwl Branch/Commit ID: 2d54b11cc9891c9aa52515fe4f8cd9cba12c6629 |
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Per-region pindel
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![]() Path: definitions/subworkflows/pindel_cat.cwl Branch/Commit ID: 3f3b186da9bf82a5e2ae74ba27aef35a46174ebe |
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kmer_build_tree
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![]() Path: task_types/tt_kmer_build_tree.cwl Branch/Commit ID: 7b5130d2408bce82ee15c666b37d931ef6f452e3 |
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scatter-valuefrom-wf3.cwl#main
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![]() Path: cwltool/schemas/v1.0/v1.0/scatter-valuefrom-wf3.cwl Branch/Commit ID: efb40a812cdba2df6699f130ee5aeea9b63045cd Packed ID: main |
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BLAST against rRNA db
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![]() Path: bacterial_noncoding/wf_blastn.cwl Branch/Commit ID: 6fad27f92dd604eca0e341178f594a560d70953b |
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Super-enhancer post ChIP-Seq analysis
Super-enhancers, consist of clusters of enhancers that are densely occupied by the master regulators and Mediator. Super-enhancers differ from typical enhancers in size, transcription factor density and content, ability to activate transcription, and sensitivity to perturbation. Use to create stitched enhancers, and to separate super-enhancers from typical enhancers using sequencing data (.bam) given a file of previously identified constituent enhancers (.gff) |
![]() Path: workflows/super-enhancer.cwl Branch/Commit ID: 44214a9d02e6d85b03eb708552ed812ae3d4a733 |
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cluster_blastp_wnode and gpx_qdump combined
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![]() Path: task_types/tt_cluster_and_qdump.cwl Branch/Commit ID: a7fced3ed8c839272c8f3a8db9da7bc8cd50271f |
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etl.cwl
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![]() Path: workflows/checkout_workflow/etl.cwl Branch/Commit ID: 18affdd927cc388fab2c113dc2ec6df782af2a52 |
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Run tRNAScan
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![]() Path: bacterial_trna/wf_trnascan.cwl Branch/Commit ID: 9144d08fa7f4e852498761481dceab477167fa65 |
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step-valuefrom2-wf.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/step-valuefrom2-wf.cwl Branch/Commit ID: efb40a812cdba2df6699f130ee5aeea9b63045cd |