Fig. 9From: An ensemble approach to accurately detect somatic mutations using SomaticSeqCADD scores from SomaticSeq’s PASS (high confidence) calls vs. LowQual (medium confidence) vs. REJECT (likely false positive) calls. a COLO-829. b CLL1. Only non-synonymous SNVs were evaluated. The p-values were calculated from a two-sided Wilcoxon rank-sum testBack to article page