Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View | 
|---|---|---|---|
|  | Bisulfite QC tools 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/bisulfite_qc.cwl Branch/Commit ID: 038cb3617a1966a1057386adcde97ce55d9e1139 | |
|  | Exome QC workflow 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/qc_exome_no_verify_bam.cwl Branch/Commit ID: cfdcd0735e8fb1ac0b97f1a5cbe0cc7e00033dd0 | |
|  | 1st-workflow.cwl 
 |  https://github.com/common-workflow-language/cwltool.git Path: cwltool/schemas/v1.0/examples/1st-workflow.cwl Branch/Commit ID: 7bfe73a708dbf31d037303bb5a8fed1a79984b0f | |
|  | 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 |  https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: 3bb0693076adc1543079a6b136c74906ad546ac6 | |
|  | exome alignment and tumor-only variant detection 
 |  https://github.com/litd/analysis-workflows.git Path: definitions/pipelines/tumor_only_exome.cwl Branch/Commit ID: 0d4e517d7c1c6deb0db02d3746c8ed4db841bd57 | |
|  | Exome QC workflow 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/qc_exome.cwl Branch/Commit ID: 3a287b7cb6162cdea79865235d224fea45963d87 | |
|  | gather AML trio outputs 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/gathered_cle_aml_trio.cwl Branch/Commit ID: 6f9f8a2057c6a9f221a44559f671e87a75c70075 | |
|  | count-lines8-wf.cwl 
 |  https://github.com/common-workflow-language/cwltool.git Path: cwltool/schemas/v1.0/v1.0/count-lines8-wf.cwl Branch/Commit ID: 216fbe57afcf67d81c99b49c1aa3aee0844f0a6a | |
|  | Tumor-Only Detect Variants workflow 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/tumor_only_detect_variants.cwl Branch/Commit ID: 8438316338e66823e1c9aca9f675b2bf33f2aa59 | |
|  | exome alignment and germline variant detection 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: 3b6d0475c80f5e452793a46a38ee188742b86595 | 
