Abstract
AbstractAccurate prediction of biological age from DNA methylation data is a critical endeavor in understanding the molecular mechanisms of aging and developing age-related disease interventions. Traditional epigenetic clocks rely on linear regression or basic machine learning models, which often fail to capture the complex, non-linear interactions within methylation data. This study introduces DeepAge, a novel deep learning framework utilizing Temporal Convolutional Networks (TCNs) to enhance the prediction of biological age from DNA methylation profiles using selected CpGs by a Dual-Correlation based apparoach. DeepAge leverages a sequence-based approach with dilated convolutions to effectively capture long-range dependencies between CpG sites, addressing the limitations of prior models by incorporating advanced network architectures including residual connections and dropout regularization. The dual correlation feature selection enhances our model’s predictive capabilities by identifying the most age-relevant CpG sites. Our model outperforms existing epigenetic clocks across multiple datasets, offering significant improvements in accuracy and providing deeper insights into the epigenetic determinants of aging. The proposed method not only sets a new standard in age estimation but also highlights the potential of deep learning in biologically relevant feature extraction and interpretation, contributing to the broader field of computational biology and precision medicine.
Publisher
Cold Spring Harbor Laboratory