Fig. 7From: Establishing analytical validity of BeadChip array genotype data by comparison to whole-genome sequence and standard benchmark datasetsPlot of the average percentage of bases within each MAP59 gene covered by whole genome sequencing (rWGS) to a read depth of A ×10 or more (gte10x) B ×20 or more (gte20x) among the 263 samples. Each rWGS nucleotide was required to have a Phred-based quality score of greater than 30 to be considered for this analysisBack to article page