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. 2017 Oct 23;18:811. doi: 10.1186/s12864-017-4159-7

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© The Author(s). 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 4 — Identification of DNA methylation levels by double capture followed by bisulfite sequencing. Correlation of DNA methylation levels at a region on chr11 (a-c) and on the MHC region (d-e) identified by dCATCH-BSseq (y-axis) and whole-genome bisulfite-sequencing (WGBS, x-axis) techniques in the CpG, CHG and CHH dinucleotide contexts, respectively. Colorful dots shown in A-D denote the density of DNA methylation sites, and histograms shown outside the axes denote the distribution of DNA methylation levels