Workflow: merge and annotate svs with population allele freq
Fetched 2025-08-17 05:45:53 GMT
Verified with cwltool version 3.1.20230201224320
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- |
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- Inputs/Outputs
This workflow is Open Source and may be reused according to the terms of:
MIT License
Note that the tools invoked by the workflow may have separate licenses.
Inputs
| ID | Type | Title | Doc |
|---|---|---|---|
| vcfs | File[] | ||
| sv_db | File | ||
| same_type | Boolean | ||
| cohort_name | String (Optional) | ||
| same_strand | Boolean | ||
| minimum_sv_size | Integer | ||
| minimum_sv_calls | Integer | ||
| estimate_sv_distance | Boolean | ||
| max_distance_to_merge | Integer |
Steps
| ID | Runs | Label | Doc |
|---|---|---|---|
| merge_vcfs |
../tools/survivor.cwl
(CommandLineTool)
|
Run SURVIVOR to merge SV calls | |
| add_population_frequency |
../tools/add_sv_population_frequency.cwl
(CommandLineTool)
|
add population allele frequencies to a vcf |
Outputs
| ID | Type | Label | Doc |
|---|---|---|---|
| merged_annotated_vcf | File |
Permalink:
https://w3id.org/cwl/view/git/60d8a9e6c5f571ec9b37f10290a1f4613013f3e1/definitions/subworkflows/merge_svs.cwl
