Fig. 4From: PureCN: copy number calling and SNV classification using targeted short read sequencingB-allele plot of the male breast cancer primary tumor sample. Panels are as described in Fig. 3, but data is for the matched primary tumor run in tumor-only mode, without the matching normal sample. The lower purity results in log-ratios and B-allele frequencies closer to 0 and 0.5, respectivelyBack to article page