Abstract

BackgroundWhole genome sequencing of bisulfite converted DNA (‘methylC-seq’) method provides comprehensive information of DNA methylation. An important application of these whole genome methylation maps is classifying each position as a methylated versus non-methylated nucleotide. A widely used current method for this purpose, the so-called binomial method, is intuitive and straightforward, but lacks power when the sequence coverage and the genome-wide methylation level are low. These problems present a particular challenge when analyzing sparsely methylated genomes, such as those of many invertebrates and plants.ResultsWe demonstrate that the number of sequence reads per position from methylC-seq data displays a large variance and can be modeled as a shifted negative binomial distribution. We also show that DNA methylation levels of adjacent CpG sites are correlated, and this similarity in local DNA methylation levels extends several kilobases. Taking these observations into account, we propose a new method based on Bayesian classification to infer DNA methylation status while considering the neighborhood DNA methylation levels of a specific site. We show that our approach has higher sensitivity and better classification performance than the binomial method via multiple analyses, including computational simulations, Area Under Curve (AUC) analyses, and improved consistencies across biological replicates. This method is especially advantageous in the analyses of sparsely methylated genomes with low coverage.ConclusionsOur method improves the existing binomial method for binary methylation calls by utilizing a posterior odds framework and incorporating local methylation information. This method should be widely applicable to the analyses of methylC-seq data from diverse sparsely methylated genomes. Bis-Class and example data are provided at a dedicated website (http://bibs.snu.ac.kr/software/Bisclass).Electronic supplementary materialThe online version of this article (doi:10.1186/1471-2164-15-608) contains supplementary material, which is available to authorized users.

Highlights

  • Whole genome sequencing of bisulfite converted DNA (‘methylC-seq’) method provides comprehensive information of DNA methylation

  • This method is based upon the particular chemical properties of DNA methylation to ‘protect’ cytosines from converting to uracils by sodium bisulfite [3]

  • During the sodium bisulfite conversion process, non-methylated cytosines are changed to uracils, which change to thymine after PCR amplification

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Summary

Introduction

Whole genome sequencing of bisulfite converted DNA (‘methylC-seq’) method provides comprehensive information of DNA methylation. A widely used current method for this purpose, the so-called binomial method, is intuitive and straightforward, but lacks power when the sequence coverage and the genome-wide methylation level are low. These problems present a particular challenge when analyzing sparsely methylated genomes, such as those of many invertebrates and plants. A method widely gaining popularity is the whole genome sequencing of bisulfite converted genomic DNA, often referred to as ‘methylC-seq’ ( referred to as ‘BS-seq’ elsewhere) This method is based upon the particular chemical properties of DNA methylation to ‘protect’ cytosines from converting to uracils by sodium bisulfite [3]. Following a sodium bisulfite treatment, nonmethylated cytosines should be read as thymines while methylated cytosines should remain as cytosines

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