Figure 4
From: Identification of copy number variants from exome sequence data
Sensitivity versus false positive rate for CNV prediction. (a) ExomeCopy. (b) ExCopyDepth. (c) Intersection of ExomeCopy and ExCopyDepth (overlapping CNVs predicted by ExomeCopy and ExCopydepth). (d) ExomeDepth. (e) CoNIFER. (f) XHMM. Sensitivity = true positive CNVs/(true positive CNVs + false negative CNVs). False positive rate = false positive CNVs/(false positive CNVs + true positive CNVs).