Figure 4
From: Variant discovery in targeted resequencing using whole genome amplified DNA
Genotype concordance metrics of downsampled subsetted WGA BAMs. Median values of NRS and NRD metrics for SNP and INDEL variants calculated from 100 bootstrap subsampled BAM files from whole-exome and chr12 capture experiments for WGA DNA samples. Plot also includes NRS and NRD metrics of the WGA subsetted BAM that matched the starting read count of the genomic sample.