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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. 3 — Double capture and sequencing of the MHC region in the GM12878 genome. a Genome-wide distribution of read coverage in GM12878 genome for dCATCH-Seq. Red bars shown above chromosomes represent the read coverage in 5 kb windows. Black bars shown below chromosomes represent the gap (unassembled) regions in reference human genome. b Scatterplot of read counts (log2-transformed) for both alleles called among heterozygous variants called within the MHC region. Colors in a rainbow mode represent the density of heterozygous variants