Figure 2From: Effective normalization for copy number variation detection from whole genome sequencingComparison of analysis outputs. Our analysis pipeline which compares the results from analyzing results from three FREEC modes. cCNV merges all the output regions for the three. cCNV segments are characterized with respect to coverage and overlap overall, in genic and non-genic regions, and in the context of the 8,599 validated segments from [11].Back to article page