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Somatic copy number variant discovery (CNVs)
Geraldine_VdAuwera Cambridge, MAMember, Administrator, Broadie admin
edited March 2018 in Best Practices Workflows
Identify somatic copy number variant (CNVs) in a case sample. Requires an appropriate Panel of Normals (PON).
|Somatic CNV case sample||Case BAM to CNV||universal||yes||b37|
|Somatic CNV PON creation||Normal BAMs to PON||universal||yes||b37|
Documentation for these workflows is in development.
Post edited by Geraldine_VdAuwera on