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. 2017 Jul 13;7:5278. doi: 10.1038/s41598-017-05702-5

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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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Summary of basic sequencing data. (A) Density of total mapped reads (W and H). X-axis represents position on chromosome (million base pairs), and Y-axis represents log2(median reads density). Green and red regions represent positive and negative strands of chromosome, respectively. (B) Percentage of reads mapped to different genome regions (W and H). (C) Percentage of genes with different expression levels (W and H). (D) Distribution of alternative splicing events and associated genes in W and H samples. The orange and the purple bars indicate the number of alternative splicing events identified in W and H libraries, respectively. The cyan and the spring green bars indicate the number of genes associated with each type of the 12 alternative splicing events. (E) Distribution of SNPs identified in W and H libraries. The red and the slate blue bars indicate the number of SNPs in W and H libraries, respectively.