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. Author manuscript; available in PMC: 2014 Feb 14.
Published in final edited form as: Cell. 2013 Feb 14;152(4):703–713. doi: 10.1016/j.cell.2013.01.035

Figure 1. Genome-wide CMS.

Figure 1

CMSGW scores calculated from full genome sequence data from the 1000 Genomes Consortium in samples from (A) Northern Europe, (B) East Asia, and (C) West Africa. The y-axis represents the significance level (p-value on -log10 scale) for each of the variants tested across the genome, showing only variants with significance levels exceeding 10−4 (corresponding to 4 on the y-axis). See also Table S1.