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. 2020 Mar 9;215(1):143–171. doi: 10.1534/genetics.120.303137

Figure 5.

Figure 5

Ability of paired (|SSH12|,, H2Tot/H1Tot) values to infer the most probable number of sweeping haplotypes ν in a shared sweep. Most probable ν for each test point was assigned from the posterior distribution of 5×106 sweep replicates with ν{0,1,,16}, drawn uniformly at random. (Top row) Ancestral sweeps for the CEU-GIH model (τ=1100, τ/(2Ne)=0.055 coalescent units, left) and the CEU-YRI model (τ=3740, τ/(2Ne)=0.0935 coalescent units, right), with t[1140,3000] (t/(2Ne)[0.057,0.15] coalescent units, left) and t[3780,5000] (t/(2Ne)[0.0945,0.125] coalescent units, right). (Bottom row) Convergent sweeps for the CEU-GIH model (left) and the CEU-YRI model (right), with t[200,1060] (t/(2Ne)[0.01,0.053] coalescent units, left) and t[200,3700] (t/(2Ne)[0.005,0.0925] coalescent units, right). Colored in red are points whose paired (|SSH12|, H2Tot/H1Tot) values are more likely to result from hard sweeps, those colored in shades of blue are points more likely to be generated from soft sweeps, and gray indicates a greater probability of neutrality. Regions in white are those for which no observations of sweep replicates within a Euclidean distance of 0.1 exist.