Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
Run genomic CMsearch (5S rRNA)
|
Path: bacterial_noncoding/wf_gcmsearch.cwl Branch/Commit ID: 551493f5c24b757a46cd22821a05e6ac6dcceb7f |
|
|
|
Filter single sample sv vcf from paired read callers(Manta/Smoove)
|
Path: definitions/subworkflows/sv_paired_read_caller_filter.cwl Branch/Commit ID: b7d9ace34664d3cedb16f2512c8a6dc6debfc8ca |
|
|
|
Varscan Workflow
|
Path: definitions/subworkflows/varscan_germline.cwl Branch/Commit ID: 5cb188131f786ed33156e2f0e3dd63ab9c04245d |
|
|
|
Merge, annotate, and generate a TSV for SVs
|
Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: b7d9ace34664d3cedb16f2512c8a6dc6debfc8ca |
|
|
|
phase VCF
|
Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: 6f9f8a2057c6a9f221a44559f671e87a75c70075 |
|
|
|
RNA-Seq alignment and transcript/gene abundance workflow
|
Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 6f9f8a2057c6a9f221a44559f671e87a75c70075 |
|
|
|
Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
|
Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 6f9f8a2057c6a9f221a44559f671e87a75c70075 |
|
|
|
exome alignment and germline variant detection, with optitype for HLA typing
|
Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: 6f9f8a2057c6a9f221a44559f671e87a75c70075 |
|
|
|
js_output_workflow.cwl
|
Path: tests/wf/js_output_workflow.cwl Branch/Commit ID: 2dce710246e091f0189fab41b589ee062ee94500 |
|
|
|
Bisulfite QC tools
|
Path: definitions/subworkflows/bisulfite_qc.cwl Branch/Commit ID: a59a803e1809a8fbfabca6b8962a8ad66dd01f1d |
