Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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kmer_top_n_extract
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![]() Path: task_types/tt_kmer_top_n_extract.cwl Branch/Commit ID: af78bfbc7625a817a2875e87c8ee267cf46b8c57 |
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env-wf2.cwl
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![]() Path: v1.0/v1.0/env-wf2.cwl Branch/Commit ID: fe164457f370c2dfec5156f6d6d45818d53cb871 |
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transcriptome_assemble.cwl
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![]() Path: workflow/transcriptome_assemble/transcriptome_assemble.cwl Branch/Commit ID: 4c90bc270e271b24caacaf000116727ff8ec81f8 |
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sec-wf.cwl
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![]() Path: tests/wf/sec-wf.cwl Branch/Commit ID: 814bd0405a7701efc7d63e8f0179df394c7766f7 |
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Bacterial Annotation, pass 3, structural annotation, functional annotation: ab initio GeneMark, by WP, by HMM (second pass)
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![]() Path: bacterial_annot/wf_bacterial_annot_pass3.cwl Branch/Commit ID: f225cd99b0e0a5043dd102f8b33a6139fefe9ea4 |
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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: 5e7385b8cfa4ddae822fff37b6bd22eb0370b389 |
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mutect parallel workflow
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![]() Path: definitions/subworkflows/mutect.cwl Branch/Commit ID: eb0092603bf57acb7bda08a06e4f2f1e2a8c9b6d |
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kmer_ref_compare_wnode
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![]() Path: task_types/tt_kmer_ref_compare_wnode.cwl Branch/Commit ID: 0514ffe248dd11068a3f2268bc67b6ce5ab051d2 |
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BLAST against rRNA db
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![]() Path: bacterial_noncoding/wf_blastn.cwl Branch/Commit ID: f225cd99b0e0a5043dd102f8b33a6139fefe9ea4 |
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Add snv and indel bam-readcount files to a vcf
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![]() Path: definitions/subworkflows/vcf_readcount_annotator.cwl Branch/Commit ID: eb0092603bf57acb7bda08a06e4f2f1e2a8c9b6d |