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. 2017 Jul 7;45(15):8697–8711. doi: 10.1093/nar/gkx587

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© The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 6. — Differentially methylated CpGs/regions in Alu and LINE-1. (A) Scatter plot comparing extended CpGs in Alu and LINE-1 between breast tumor and matched normal tissue; significant differences at Bonferroni P < 0.05 are colored and n is the number of CpGs (orange: hypermethylated; blue: hypomethylated). (B) Genome-wide break down of all CpGs tested, bumps formed using bumphunter, and significant DMR (FWER < 0.05) identified in breast cancer. Genomic distribution of extended CpGs was similar to profiled and identified more DMR of interest, especially in the intron and intergenic regions.