Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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multi-psf.cwl
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![]() Path: multi-psf.cwl Branch/Commit ID: master |
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mutect2_calling.cwl
GATK4.1.2 Mutect2 workflow |
![]() Path: subworkflows/mutect2_calling.cwl Branch/Commit ID: master |
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if_input_is_bz2_generate_md5sum_else_return_input_chksum_json.cwl
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![]() Path: cwls/toolkit/if_input_is_bz2_generate_md5sum_else_return_input_chksum_json.cwl Branch/Commit ID: 0.4.0 |
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exome alignment and germline variant detection
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![]() Path: germline_exome_workflow.cwl Branch/Commit ID: toil_compatibility |
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Filter single sample sv vcf from depth callers(cnvkit/cnvnator)
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![]() Path: definitions/subworkflows/sv_depth_caller_filter.cwl Branch/Commit ID: low-vaf |
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wf_trim_partial_and_map_se.cwl
This workflow takes in appropriate trimming params and demultiplexed reads, and performs the following steps in order: trimx1, trimx2, fastq-sort, filter repeat elements, fastq-sort, genomic mapping, sort alignment, index alignment, namesort, PCR dedup, sort alignment, index alignment |
![]() Path: cwl/wf_trim_partial_and_map_se.cwl Branch/Commit ID: master |
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rRNA_selection.cwl
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![]() Path: tools/rRNA_selection.cwl Branch/Commit ID: 0fed1c9 |
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EMG pipeline v3.0 (single end version)
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![]() Path: workflows/emg-pipeline-v3.cwl Branch/Commit ID: caea457 |
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search.cwl#main
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![]() Path: tests/search.cwl Branch/Commit ID: main Packed ID: main |
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main-somatic.cwl
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![]() Path: somatic/somatic-workflow/main-somatic.cwl Branch/Commit ID: master |