ReMeDy: A Flexible Statistical Framework For Region-based Detection of DNA Methylation Dysregulation

可解释性 DNA甲基化 甲基化 计算生物学 计算机科学 平滑的 统计能力 生物导体 统计模型 回归 航程(航空) 生物 标杆管理 表观遗传学 相关性 遗传关联 数据挖掘 线性回归 核(代数) 变量(数学) 甲基转移酶 遗传学 加性模型 I类和II类错误 回归分析 全基因组关联研究 人工智能 联想(心理学)
作者
Suvo Chatterjee,Siddhant Meshram,Arunkumar Ganesan,Fasil Tekola‐Ayele,Arindam Fadikar
出处
期刊: [Cold Spring Harbor Laboratory]
标识
DOI:10.64898/2026.01.02.697394
摘要

Region-based epigenome-wide association studies have demonstrated improved statistical power and biological interpretability compared with probe-wise analyses of DNA methylation data. However, most existing region-based methods characterize methylation dysregulation primarily through changes in mean methylation levels associated with a phenotype of interest. Substantial evidence indicates that phenotype-associated methylation alterations may also manifest through changes in methylation variability or through joint shifts in mean and variability. Despite this, no existing statistical framework jointly models mean-variance methylation changes in a region-based manner. We propose ReMeDy, a flexible statistical framework that uses a hierarchical likelihood approach within a generalized linear model setting to identify differentially methylated regions, variably methylated regions, and regions exhibiting joint differential and variable methylation at a genome-wide scale. Unlike existing models, ReMeDy operates directly on biologically defined co-methylated regions, allowing it to naturally capture spatial correlation inherent in DNA methylation array data, while avoiding reliance on heuristic, user-defined tuning parameters such as smoothing spans and kernel bandwidths that can substantially influence results and introduce subjectivity. Through extensive simulation studies and comprehensive benchmarking against popular models, we demonstrate that ReMeDy maintains false discovery and type-I error rates at nominal levels while achieving consistently higher statistical power across a wide range of realistic scenarios. Application to population-level DNA methylation data further shows that ReMeDy identifies biologically meaningful regions and pathways implicated in complex human diseases that are not captured by conventional mean-based analyses alone. ReMeDy is implemented as an open-source R package and is freely available at https://github.com/SChatLab/ReMeDy.
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