Supplementary Figure 10: Editing sites and their prevalence in the 1000 Genomes data set.
From: Genome sequence–independent identification of RNA editing sites
(a) Distribution of prevalence of editing sites identified in the 1000 Genomes data set. Prevalence was defined as the fraction of individuals expressing the edited nucleotide among those with at least 10 reads covering this position. Only editing sites with a minimum read coverage of 10 in at least 50% of individuals were included. (b) Editing ratios of sites associated with different values of prevalence. The first prevalence range was set to be between 0 and 0.3 due to the small number of editing sites within the first three deciles.
