Figure 5.
Coverage of whole genome, coverage of the genotyped sites, and error rate as a function of quality filter. The consensus sequence of the Asian genome was calculated from the 36× sequencing reads. The error rate was estimated by assuming the genotyping result on the same sample was right. A false-positive (FP) is to call an incorrect allele, while a false-negative (FN) is the heterozygous site with one allele missing.
