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. 2020 Feb 20;37(6):1790–1808. doi: 10.1093/molbev/msaa038

Fig. 5.

Fig. 5.

(A) Distribution of raw error (rpredictedrtrue) for LDhelmet and ReLERNN when presented with varying levels of missing genotypes for simulations with n = 4 and (B) n = 20 chromosomes. (C) Fine-scale rate predictions generated by ReLERNN for a 1-Mb recombination landscape (gray line) simulated with varying levels of missing genotypes, for n = 4 and (D) n = 20 chromosomes.