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. 2018 Jan 10;8:384. doi: 10.1038/s41598-017-18730-y

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Methods and results of RNA editing site (RES) detection. (A) The pipeline for RNA editing site detection. (B) Number of RESs in Sample S1. The editing type is relative to DNA sequence on the Watson strand. We used a non-strand-specific mRNA-seq method; therefore, it is not clear whether these mRNA transcripts are from the Watson or Crick strand. Ensembl gene annotation is used as a reference. (C) Distribution of the RESs located in genes.