Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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process VCF workflow
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![]() Path: definitions/subworkflows/strelka_process_vcf.cwl Branch/Commit ID: 06d2440d115b446c299b4ce96e8812d2f8df86ec |
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Unaligned to aligned BAM
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![]() Path: definitions/subworkflows/align.cwl Branch/Commit ID: 06d2440d115b446c299b4ce96e8812d2f8df86ec |
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Seed Search Compartments
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![]() Path: protein_alignment/wf_seed.cwl Branch/Commit ID: 5ec226c941562124032ca6861bc8d1aeabf9d91a |
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step-valuefrom3-wf.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/step-valuefrom3-wf.cwl Branch/Commit ID: 84939620c3eec1ab11369849c63237ebfa48da41 |
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wf_get_peaks_pe.cwl
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![]() Path: cwl/wf_get_peaks_pe.cwl Branch/Commit ID: b2b95f58f96ee5b34bd9b342d0ecda63d135e278 |
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wf_get_peaks_scatter_se.cwl
The \"main\" workflow. Takes fastq files generated using the seCLIP protocol (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991800/) and outputs candidate RBP binding regions (peaks). runs: wf_get_peaks_se.cwl through scatter across multiple samples. |
![]() Path: cwl/wf_get_peaks_scatter_se.cwl Branch/Commit ID: b2b95f58f96ee5b34bd9b342d0ecda63d135e278 |
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fp_filter workflow
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![]() Path: definitions/subworkflows/fp_filter.cwl Branch/Commit ID: 27dcb1ae121be6a23057b74332b8c752ea425735 |
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scatter GATK HaplotypeCaller over intervals
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![]() Path: definitions/subworkflows/gatk_haplotypecaller_iterator.cwl Branch/Commit ID: bed420556091b7b8b45cf20a95e5947e1de9a416 |
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wf_demultiplex_pe.cwl
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![]() Path: cwl/wf_demultiplex_pe.cwl Branch/Commit ID: 6b533898c395e9e5b9d0acc1587d0c68bc56abe0 |
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Filter single sample sv vcf from paired read callers(Manta/Smoove)
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![]() Path: definitions/subworkflows/sv_paired_read_caller_filter.cwl Branch/Commit ID: 06d2440d115b446c299b4ce96e8812d2f8df86ec |