Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
02-trim-pe.cwl
ATAC-seq 02 trimming - reads: PE |
Path: v1.0/ATAC-seq_pipeline/02-trim-pe.cwl Branch/Commit ID: 46e5078373d4668019485d27c71770aec9dd9f0e |
|
|
|
1st-workflow.cwl
|
Path: tests/wf/1st-workflow.cwl Branch/Commit ID: fc6ca8b1498926f705dcfde7ab0a365bd09a9675 |
|
|
|
tt_hmmsearch_wnode.cwl
|
Path: task_types/tt_hmmsearch_wnode.cwl Branch/Commit ID: 68311dd5328bf6b782a370a0253b41062a3359a3 |
|
|
|
bqsr-flow-distr.cwl
Run BQSR pre+post+plot flow with distribution |
Path: stage/bqsr-flow-distr.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: b9e7392e72506cadd898a6ac4db330baf6535ab6 |
|
|
|
tt_fscr_calls_pass1
|
Path: task_types/tt_fscr_calls_pass1.cwl Branch/Commit ID: e351f650524b532f85820b8e53855010b35046c2 |
|
|
|
exome alignment and somatic variant detection
|
Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: c235dc6d623879a6c4f5fb307f545c9806eb2d23 |
|
|
|
Apply filters to VCF file
|
Path: definitions/subworkflows/filter_vcf_mouse.cwl Branch/Commit ID: 0b0ad1a54f0f6849dc645449b079470448a23095 |
|
|
|
fp_filter workflow
|
Path: definitions/subworkflows/fp_filter.cwl Branch/Commit ID: a28a8077a8c4dbf117d16799807483a2532af3f3 |
|
|
|
merge and annotate svs with population allele freq
|
Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: e509210450e4c62aecb99a228fc97f0eae2d9580 |
