Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View | 
|---|---|---|---|
|  | 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: 449bc7e45bb02316d040f73838ef18359e770268 | |
|  | downsample unaligned BAM and align 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/downsampled_alignment.cwl Branch/Commit ID: ac87e0584685fe04e4010ecd77ae4f055f21d788 | |
|  | Detect Variants workflow 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/detect_variants.cwl Branch/Commit ID: 449bc7e45bb02316d040f73838ef18359e770268 | |
|  | Detect Variants workflow 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/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: 8438316338e66823e1c9aca9f675b2bf33f2aa59 | |
|  | Tumor-Only Detect Variants workflow 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/tumor_only_detect_variants.cwl Branch/Commit ID: 3b6d0475c80f5e452793a46a38ee188742b86595 | |
|  | dynresreq-workflow-stepdefault.cwl 
 |  https://github.com/common-workflow-language/common-workflow-language.git Path: v1.0/v1.0/dynresreq-workflow-stepdefault.cwl Branch/Commit ID: ca8e6661b5cab1f017e5bc4024650722dae4d50b | |
|  | exome alignment and germline variant detection 
 |  https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: eb0092603bf57acb7bda08a06e4f2f1e2a8c9b6d | |
|  | report-wf.cwl 
 |  https://github.com/arvados/arvados-tutorial.git Path: WGS-processing/cwl/helper/report-wf.cwl Branch/Commit ID: b50ffeeeae865d0780ca03c5a3f5065eeeb758e4 | |
|  | tt_fscr_calls_pass1 
 |  https://github.com/ncbi/pgap.git Path: task_types/tt_fscr_calls_pass1.cwl Branch/Commit ID: 47ccbd0bc7b45bf8b3c92d0a66c1a9a232367a5d | 
