Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
pipeline.cwl
|
Path: pipeline.cwl Branch/Commit ID: 20ea8da |
|
|
|
sorter.cwl
|
Path: steps/sorter.cwl Branch/Commit ID: master |
|
|
|
somatic_exome: exome alignment and somatic variant detection
somatic_exome is designed to perform processing of mutant/wildtype H.sapiens exome sequencing data. It features BQSR corrected alignments, 4 caller variant detection, and vep style annotations. Structural variants are detected via manta and cnvkit. In addition QC metrics are run, including somalier concordance metrics. example input file = analysis_workflows/example_data/somatic_exome.yaml |
Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: master |
|
|
|
bam-genomecov-bigwig.cwl
creates genome coverage bigWig file from .bam file |
Path: workflows/bam-genomecov-bigwig.cwl Branch/Commit ID: v0.0.2 |
|
|
|
step-valuefrom3-wf.cwl
|
Path: v1.0/v1.0/step-valuefrom3-wf.cwl Branch/Commit ID: master |
|
|
|
wf_makeblastdb.cwl
|
Path: amr_finder/wf_makeblastdb.cwl Branch/Commit ID: master |
|
|
|
Identifies non-coding RNAs using Rfams covariance models
|
Path: workflows/cmsearch-multimodel-wf.cwl Branch/Commit ID: master |
|
|
|
main.cwl
|
Path: main.cwl Branch/Commit ID: master |
|
|
|
process VCF workflow
|
Path: strelka/process_vcf.cwl Branch/Commit ID: toil_compatibility |
|
|
|
Seed Protein Alignments
|
Path: protein_alignment/wf_seed_seqids.cwl Branch/Commit ID: master |
