Risk Alleles Workflow
Runs the workflow to automate discovery, annotation, and report creation for Risk variants for exomes and genomes.
Input Parameters
Type | Name | Req’d | Description |
---|---|---|---|
File | input_cram | Yes | Sample CRAM/BAM file to run the workflow on |
File | input_crai | Yes | Corresponding CRAI/BAI file to the CRAM/BAM file |
String | sample_id | Yes | Full sample identifier |
String | accession_id | Yes | Sample accession (PM#) |
Stri |
This is a companion discussion topic for the original entry at github.com/mgbpm/biofx-workflows/RiskAllelesWorkflow