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2020 | OriginalPaper | Chapter

LuxHS: DNA Methylation Analysis with Spatially Varying Correlation Structure

Authors : Viivi Halla-aho, Harri Lähdesmäki

Published in: Bioinformatics and Biomedical Engineering

Publisher: Springer International Publishing

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Abstract

Bisulfite sequencing (BS-seq) is a popular method for measuring DNA methylation in basepair-resolution. Many BS-seq data analysis tools utilize the assumption of spatial correlation among the neighboring cytosines’ methylation states. While being a fair assumption, most existing methods leave out the possibility of deviation from the spatial correlation pattern. Our approach builds on a method which combines a generalized linear mixed model (GLMM) with a likelihood that is specific for BS-seq data and that incorporates a spatial correlation for methylation levels. We propose a novel technique using a sparsity promoting prior to enable cytosines deviating from the spatial correlation pattern. The method is tested with both simulated and real BS-seq data and compared to other differential methylation analysis tools.

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Metadata
Title
LuxHS: DNA Methylation Analysis with Spatially Varying Correlation Structure
Authors
Viivi Halla-aho
Harri Lähdesmäki
Copyright Year
2020
DOI
https://doi.org/10.1007/978-3-030-45385-5_45

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