| Literature DB >> 22290186 |
Felix Krueger1, Benjamin Kreck, Andre Franke, Simon R Andrews.
Abstract
Bisulfite conversion of genomic DNA combined with next-generation sequencing (BS-seq) is widely used to measure the methylation state of a whole genome, the methylome, at single-base resolution. However, analysis of BS-seq data still poses a considerable challenge. Here we summarize the challenges of BS-seq mapping as they apply to both base and color-space data. We also explore the effect of sequencing errors and contaminants on inferred methylation levels and recommend the most appropriate way to analyze this type of data.Entities:
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Year: 2012 PMID: 22290186 DOI: 10.1038/nmeth.1828
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547