HBCR_DMR: A Hybrid Method Based on Beta-Binomial Bayesian Hierarchical Model and Combination of Ranking Method to Detect Differential Methylation Regions in Bisulfite Sequencing Data

TL;DR

This paper introduces HBCR_DMR, a new method combining Bayesian modeling and ranking techniques to accurately detect DNA methylation differences between sample groups.

Contribution

The novel hybrid approach integrates beta-binomial Bayesian modeling with a ranking-based voting system for improved DMR detection.

Findings

HBCR_DMR achieved a sensitivity of 0.72 and specificity of 0.89 in simulations and real data.

The method demonstrated an F1 score of 0.76 and an AUC of 0.94, indicating strong performance.

The hybrid approach effectively distinguishes methylated regions across sample groups.

Abstract

DNA methylation is a key epigenetic modification involved in gene regulation, contributing to both physiological and pathological conditions. For a more profound comprehension, it is essential to conduct a precise comparison of DNA methylation patterns between sample groups that represent distinct statuses. Analysis of differentially methylated regions (DMRs) using computational approaches can help uncover the precise relationships between these phenomena. This paper describes a hybrid model that combines the beta-binomial Bayesian hierarchical model with a combination of ranking methods known as HBCR_DMR. During the initial phase, we model the actual methylation proportions of the CpG sites (CpGs) within the replicates. This modeling is achieved through beta-binomial distribution, with parameters set by a group mean and a dispersion parameter. During the second stage, we establish the selection of distinguishing CpG sites based on their methylation status, employing multiple ranking techniques. Finally, we combine the ranking lists of differentially methylated CpG sites through a voting system. Our analyses, encompassing simulations and real data, reveal outstanding performance metrics, including a sensitivity of 0.72, specificity of 0.89, and an F1 score of 0.76, yielding an overall accuracy of 0.82 and an AUC of 0.94. These findings underscore HBCR_DMR’s robust capacity to distinguish methylated regions, confirming its utility as a valuable tool for DNA methylation analysis.

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