Fig. 5From: Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing dataMapping precision of GWAS based on imputations with different sample sizes of the reference panel. Shown are results from 50,000 simulations for common (a) and rare (b) variants, respectively. 1KGP3 (n ref = 1000) and 1KGP3 (n ref = 500): SNP array data imputed to a random subset of 1000 and 500 individuals randomly sampled from 1KGP3, respectivelyBack to article page