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. 2013 Jan 30;30(5):1145–1158. doi: 10.1093/molbev/mst016

Fig. 2.

Fig. 2.

Comparison of the EM algorithm to known allele-frequency-based and simple-sequence-based methods. Each algorithm was run on simulated pooled 100-bp paired-end sequence data from 20 haplotypes at 200× coverage, with 100 replicates for each region width.