Figures
The legends for Figures 3 and 4 are switched. The authors have provided corrected versions here.
The chromatograms of PRRT2 sequence before (Native DNA) and after whole genome amplification of the DNA from three independent patients using two different protocols GenomiPhi DNA Amplification Kit (WGA-1) or Repli-G Whole Genome Amplification kit (WGA-2). The mutation was not present in the native DNA, but was detected after whole genome amplification.
A. Nonsynonymous mutations per nonsynonymous sites (pN) and synonymous mutations per synonymous sites (pS) were estimated using the data from 4300 individuals from European ancestry and 2012 individuals from African ancestry available at the Exome Variant Server (http://evs.gs.washington.edu/EVS/). The horizontal lanes correspond to the means of pN and pS for the 27 genes. Difference of pN/pS between Europe and Africa were calculated using a 2-tailed Fisher exact test and the –Log10 P value is indicated. B. Plot of the –Log10 P values obtained for the difference between the pN/pS ratio in Africa and in Europe in relation the ratio (Europe pN/pS) / (Africa pN/pS).
Reference
Citation: The PLOS ONE Staff (2014) Correction: Heterogeneous Pattern of Selective Pressure for PRRT2 in Human Populations, but No Association with Autism Spectrum Disorders. PLoS ONE 9(6): e100607. https://doi.org/10.1371/journal.pone.0100607
Published: June 12, 2014
Copyright: © 2014 The PLOS ONE Staff. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.