LuxUS: DNA methylation analysis using generalized linear mixed model with spatial correlation

DNA甲基化 表观遗传学 亚硫酸氢盐测序 计算生物学 胞嘧啶 甲基化 生物 DNA 遗传学 计算机科学 基因 基因表达
作者
Viivi Halla-aho,Harri Lähdesmäki
出处
期刊:Bioinformatics [Oxford University Press]
卷期号:36 (17): 4535-4543 被引量:4
标识
DOI:10.1093/bioinformatics/btaa539
摘要

DNA methylation is an important epigenetic modification, which has multiple functions. DNA methylation and its connections to diseases have been extensively studied in recent years. It is known that DNA methylation levels of neighboring cytosines are correlated and that differential DNA methylation typically occurs rather as regions instead of individual cytosine level.We have developed a generalized linear mixed model, LuxUS, that makes use of the correlation between neighboring cytosines to facilitate analysis of differential methylation. LuxUS implements a likelihood model for bisulfite sequencing data that accounts for experimental variation in underlying biochemistry. LuxUS can model both binary and continuous covariates, and mixed model formulation enables including replicate and cytosine random effects. Spatial correlation is included to the model through a cytosine random effect correlation structure. We show with simulation experiments that using the spatial correlation, we gain more power to the statistical testing of differential DNA methylation. Results with real bisulfite sequencing dataset show that LuxUS is able to detect biologically significant differentially methylated cytosines.The tool is available at https://github.com/hallav/LuxUS.Supplementary data are available at Bioinformatics online.
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