Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
---|---|---|---|
umi molecular alignment workflow
|
https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/molecular_qc.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
||
scatter-wf3.cwl#main
|
https://github.com/common-workflow-language/cwl-v1.1.git
Path: tests/scatter-wf3.cwl Branch/Commit ID: 368b562a1449e8cd39ae8b7f05926b2bfb9b22df Packed ID: main |
||
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: 04d21c33a5f2950e86db285fa0a32a6659198d8a |
||
step-valuefrom-wf.cwl
|
https://github.com/common-workflow-language/common-workflow-language.git
Path: v1.0/v1.0/step-valuefrom-wf.cwl Branch/Commit ID: f02557902989c749c9c2187c7045e340e2d76bfc |
||
wgs alignment with qc
|
https://github.com/genome/cancer-genomics-workflow.git
Path: wgs_alignment.cwl Branch/Commit ID: ab3cc1f460146c60d7de417508f0c1ea70506e6a |
||
gather AML trio outputs
|
https://github.com/tmooney/cancer-genomics-workflow.git
Path: definitions/pipelines/aml_trio_cle_gathered.cwl Branch/Commit ID: 233f026ffce240071edda526391be0c03186fce8 |
||
mutect panel-of-normals workflow
|
https://github.com/genome/analysis-workflows.git
Path: definitions/pipelines/panel_of_normals.cwl Branch/Commit ID: 844c10a4466ab39c02e5bfa7a210c195b8efa77a |
||
exome alignment and germline variant detection
|
https://github.com/tmooney/cancer-genomics-workflow.git
Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: 233f026ffce240071edda526391be0c03186fce8 |
||
exome alignment and tumor-only variant detection
|
https://github.com/genome/analysis-workflows.git
Path: definitions/pipelines/tumor_only_exome.cwl Branch/Commit ID: 0b6e8fd8ead7644cf5398395b76af5cf4011686f |
||
Unaligned to aligned BAM
|
https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/align.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |