Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
bulk-atac-seq-pipeline.cwl
|
Path: bulk-atac-seq-pipeline.cwl Branch/Commit ID: 3da5dd0 |
|
|
|
textures.cwl
Create emblem textures |
Path: textures/textures.cwl Branch/Commit ID: cwl |
|
|
|
Run genomic CMsearch
|
Path: bacterial_noncoding/wf_gcmsearch.cwl Branch/Commit ID: master |
|
|
|
scatter-valuefrom-wf5.cwl
|
Path: tests/scatter-valuefrom-wf5.cwl Branch/Commit ID: main |
|
|
|
cnv.cwl
Copynumber variation workflow, runs ADTEx and Varscan |
Path: cnv.cwl Branch/Commit ID: 1.0.1 |
|
|
|
Transcriptome assembly workflow (single-end version)
|
Path: workflows/TranscriptomeAssembly-wf.single-end.cwl Branch/Commit ID: assembly |
|
|
|
echo-wf-default.cwl
|
Path: tests/echo-wf-default.cwl Branch/Commit ID: master |
|
|
|
intersect_intervals.cwl
|
Path: cwl/workflows/intersect_intervals.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: downsample_and_recall |
|
|
|
ConcordanceCheckerWorkflow.cwl
|
Path: vcf-comparator/ConcordanceCheckerWorkflow.cwl Branch/Commit ID: 1.30.0 |
