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. 2019 Jan 16;211(3):1019–1028. doi: 10.1534/genetics.118.301684

Figure 6.

Figure 6

Estimation of s by MMC-ABC for 9500 neutral sites and 500 sites for which s=0.1 with N=1000 and Ψ=0.1, with N estimated over a uniform prior U[250,2000], Ψ estimated from the prior U[0,0.3], and s estimated over U[0.2,0.6]. Note that we display the relative frequencies for estimated values of s for each class of mutation, for which there were unequal numbers of total sites. These results demonstrate the ability of MMC-ABC to jointly and accurately estimate N, Ψ, and s from genomic data, even when a large number of sites are under positive selection.