Figure 3From: Variant discovery in targeted resequencing using whole genome amplified DNANumber of variants discovered in downsampled and subsetted WGA BAMs. Median number of SNPs and INDELs called from 100 bootstrap subsampled BAM files from whole-exome and chr12 capture experiments for WGA DNA samples. Plot also includes number of variants discovered in the WGA subsetted BAM that matched the starting read count of the genomic sample.Back to article page