Figure 5: Variant allele frequency analysis of all mutations in four tumors.
From: Independent Tumor Origin in Two Cases of Synchronous Bilateral Clear Cell Renal Cell Carcinoma
(A,B) Mutations in case BC_1. (C,D) Mutations in case BC_2. (A,C) Germline variants. (B,D) tumor-specific mutations. Each dot represents a variant allele detected in WES. The value of each dot is calculated as variant allele depth/total depth. Black dots represent SNVs and red dots represent indels. r, Pearson correlation coefficient; p < 0.05, statistically significant.
