Methylated DNA is over-represented in whole-genome bisulfite sequencing data

Lexiang Ji, Takahiko Sasaki, Xiaoxiao Sun, Ping Ma, Zachary A. Lewis, Robert J. Schmitz

Research output: Contribution to journalArticlepeer-review

40 Scopus citations

Abstract

The development of whole-genome bisulfite sequencing (WGBS) has resulted in a number of exciting discoveries about the role of DNA methylation leading to a plethora of novel testable hypotheses. Methods for constructing sodium bisulfiteconverted and amplified libraries have recently advanced to the point that the bottleneck for experiments that use WGBS has shifted to data analysis and interpretation. Here we present empirical evidence for an over-representation of reads from methylated DNA in WGBS. This enrichment for methylated DNA is exacerbated by higher cycles of PCR and is influenced by the type of uracilinsensitive DNA polymerase used for amplifying the sequencing library. Future efforts to computationally correct for this enrichment bias will be essential to increasing the accuracy of determining methylation levels for individual cytosines. It is especially critical for studies that seek to accurately quantify DNA methylation levels in populations that may segregate for allelic DNA methylation states.

Original languageEnglish (US)
Article number341
JournalFrontiers in Genetics
Volume5
Issue numberSEP
DOIs
StatePublished - 2014
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics
  • Genetics(clinical)

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