Figure 5From: Variant discovery in targeted resequencing using whole genome amplified DNAGenotype concordance metrics as a function of GC%. NRS and NRD of variants binned according to GC% based on quartiles of GC% in capture targets. First row shows NRD values for SNP and INDELs and second row shows NRS values of SNPs and INDELs for each of the chr12 and whole-exome capture experiments.Back to article page