Figure 3.
Genotyping call rates, minor allele frequencies, and concordance among platforms for CPIC important SNVs (n = 124). Each row is a genomic variant; the order of the variants (top to bottom) is the same as in Supplemental Table 2.
Genotyping call rates, minor allele frequencies, and concordance among platforms for CPIC important SNVs (n = 124). Each row is a genomic variant; the order of the variants (top to bottom) is the same as in Supplemental Table 2.