DeepMethylation: A deep learning framework for tissue-specific DNA methylation prediction and functional variant annotation
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Updated: Jul 3, 2026

Methyl-binding DNA capture Sequencing for Patient Tissues
Published on: October 31, 2016
Wenran Li1, Shijia Yu1, Yingyu Cheng1
1Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.
Abstract:
DNA methylation is a key epigenetic modification that regulates gene expression and plays a vital role in cell differentiation, development, and tumorigenesis. However, large-scale experimental profiling of genome-wide DNA methylation remains time-consuming and limited in coverage. We present DeepMethylation, a deep learning framework that integrates DNA sequence and tissue-specific epigenomic features to predict CpG methylation status across the genome. DeepMethylation achieves state-of-the-art performance (average AUROC 0.909) across tissues, accurately imputes methylation beyond array-covered sites, and enables robust extension from 450k to EPIC array coverage. Feature importance analysis revealed consistent patterns of epigenomic feature contributions across tissues. We also introduced Delta DeepMethylation (DDM), a variant evaluation model to estimate the epigenetic effects of SNPs on DNA methylation. DDM-predicted variant effects were consistent with methylation quantitative trait loci (mQTLs) and not confounded by linkage disequilibrium (LD). Our framework provides a powerful tool for genome-wide methylation prediction and regulatory variant interpretation across tissues.

