Fig. 7
From: PureCN: copy number calling and SNV classification using targeted short read sequencing
Accuracy on simulated ultra-deep sequencing data (400×) from a 560 gene panel. This shows the same plots as in Fig. 6, but forsimulated data from a targeted panel. Due to the higher sequencing depth, even the low purity samples have in general ploidy estimates close to the true ploidy