“…A simple visualization of expected and observed frequencies of homozygote genotypes across single nucleotide polymorphisms (SNPs) can be effective in identifying data problems (Figure 1). A simple model for estimating the heterozygote miscall (dropout) rate was applied to 12 publicly available RAD‐seq datasets (Fernández et al., 2016; Hecht, Matala, Hess, & Narum, 2015; Laporte et al., 2016; Larson et al., 2014; Le Moan, Gagnaire, & Bonhomme, 2016; Portnoy et al., 2015; Prince et al., 2017; Puritz, Gold, & Portnoy, 2016; Ravinet et al., 2016; Swaegers et al., 2015). While a few had low genotyping error rates (<5%), in others, allelic dropout, low read depth, PCR duplicates, erroneous assembly, and/or poor filtering resulted in much higher estimated error rates, with between 5% and 72% of heterozygotes apparently being miscalled as homozygotes.…”