* Variant calling in parallel using GATK Haplotype Caller (https://gatk.broadinstitute.org/hc/en-us)
* Generation of an HTML report comparing variants against ClinVar archive (https://www.ncbi.nlm.nih.gov/clinvar/)
-Workflows are written in CWL v1.1.
+Workflows are written in CWL v1.1. (https://www.commonwl.org/)
Subdirectories are:
* cwl - contains CWL code for the demo
To run the workflow:
-* cd into cwl directory
* run the following:
- arvados-cwl-runner --no-wait --project-uuid YOUR_PROJECT_UUID wgs-processing-wf.cwl ../yml/YOURINPUTS.yml
+ arvados-cwl-runner --no-wait --project-uuid YOUR_PROJECT_UUID ./cwl/wgs-processing-wf.cwl ./yml/YOURINPUTS.yml
About the Demo Data:
WGS Data used in this demo is public data made available by the Personal Genome Project.