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pubmed-article:19776032pubmed:abstractTextDNA methylation is known to be associated with cell differentiation, aging, disease and cancer. There exists an expanding base of knowledge regarding tissue-specific DNA methylation, but we have little information about person-specific DNA methylation. Here, we analyze the DNA methylation patterns of multiple tissues from multiple individuals using a high-throughput quantitative assay of genome-wide DNA methylation, namely the Illumina GoldenGate BeadArray. DNA methylation patterns were largely conserved across 11 different tissues (r = 0.852) and across six individuals (r = 0.829), and we found that DNA was highly methylated in non-CpG islands and/or CpG sites that are not occupied by either H3K4me3 or H3K27me3 (P < 0.05). Finally, we found that the Illumina GoldenGate assay features a large number of probes (265/1505 probes, 17.6%) that contain single-nucleotide polymorphisms, which may interfere with DNA methylation analyses in genome-wide studies.lld:pubmed
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pubmed-article:19776032pubmed:authorpubmed-author:KanelGaryGlld:pubmed
pubmed-article:19776032pubmed:authorpubmed-author:YangAllen SASlld:pubmed
pubmed-article:19776032pubmed:authorpubmed-author:ByunHyang-Min...lld:pubmed
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pubmed-article:19776032pubmed:year2009lld:pubmed
pubmed-article:19776032pubmed:articleTitleEpigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns.lld:pubmed
pubmed-article:19776032pubmed:affiliationJane Anne Nohl Division of Hematology, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.lld:pubmed
pubmed-article:19776032pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19776032pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:19776032pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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