Methods for identifying differentially methylated regions for sequence- and array-based data

Brief Funct Genomics. 2016 Nov;15(6):485-490. doi: 10.1093/bfgp/elw018. Epub 2016 Jun 20.

Abstract

DNA methylation is one of the most important epigenetic mechanisms, and participates in the pathogenic processes of many diseases. Differentially methylated regions (DMRs) in the genome have been reported and implicated in a number of different diseases, tissues and cell types, and are associated with gene expression levels. Therefore, identification of DMRs is one of the most critical and fundamental issues in dissecting the disease etiologies. Based on bisulfite conversion, advances in sequence- and array-based technologies have helped investigators study genome-wide DNA methylation. Many methods have been developed to detect DMRs, and they have revolutionized our understanding of DNA methylation and provided new insights into its role in diverse biological functions. According to data and region types, we discuss various methods in detecting DMRs, their utility and limitations comprehensively. We recommend using a few of the methods in the same data and region type to detect DMRs because they could be complementary to one another.

Keywords: DNA methylation; Illumina 450k methylation array; bisulfite sequencing; differentially methylated regions.

Publication types

  • Review

MeSH terms

  • Animals
  • DNA Methylation*
  • Epigenesis, Genetic*
  • Gene Expression Regulation*
  • Humans
  • Neoplasms / genetics*
  • Oligonucleotide Array Sequence Analysis / methods*
  • Sequence Analysis, DNA / methods*