Profiling DNA Methylomes from Microarray to Genome-Scale Sequencing

被引:41
作者
Huang, Yi-Wen [1 ]
Huang, Tim H. -M. [1 ]
Wang, Li-Shu [1 ]
机构
[1] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
关键词
DNA methylation; Microarray; Next-generation sequencing; CPG ISLAND METHYLATION; CYTOSINE METHYLATION; COLORECTAL-CANCER; BREAST-CANCER; HUMAN-CELLS; RESOLUTION; MAPS; WIDE; HYPERMETHYLATION; DIFFERENTIATION;
D O I
10.1177/153303461000900203
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA cytosine methylation is a central epigenetic modification which plays critical roles in cellular processes including genome regulation, development and disease. Here, we review current and emerging microarray and next-generation sequencing based technologies that enhance our knowledge of DNA methylation profiling. Each methodology has limitations and their unique applications, and combinations of several modalities may help build the entire methylome. With advances on next-generation sequencing technologies, it is now possible to globally map the DNA cytosine methylation at single-base resolution, providing new insights into the regulation and dynamics of DNA methylation in genomes.
引用
收藏
页码:139 / 147
页数:9
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