Germline copy number variant discovery (CNVs)
Geraldine_VdAuwera Cambridge, MAMember, Administrator, Broadie admin
edited January 2018 in Best Practices Workflows
Identify germline copy number variants.
Diagram is not available
Reference implementation is not available
This workflow is in development; detailed documentation will be made available when the workflow is considered fully released.
Post edited by Geraldine_VdAuwera on