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DeepSF-4mC: A deep learning model for predicting DNA cytosine 4mC methylation sites leveraging sequence features

Zhaomin Yao, Fei Li, Weiming Xie, Jiaming Chen, Jiezhang Wu, Ying Zhan, Xiaodan Wu, Zhiguo Wang, Guoxu Zhang

2024Computers in Biology and Medicine14 citationsDOIOpen Access PDF

Abstract

-methylcytosine (4mC) is a DNA modification involving the addition of a methyl group to the fourth nitrogen atom of the cytosine base. This modification may influence gene regulation, providing potential insights into gene control mechanisms. Traditional laboratory methods for detecting 4mC DNA methylation have limitations, but the rise of artificial intelligence has introduced efficient computational strategies for 4mC site prediction. Despite this progress, challenges persist in terms of model performance and interpretability. To tackle these challenges, we propose DeepSF-4mC, a deep learning model specifically designed for predicting DNA cytosine 4mC methylation sites by leveraging sequence features. Our approach incorporates multiple encoding techniques to enhance prediction accuracy, increase model stability, and reduce the computational resources needed. Leveraging transfer learning, we harness existing models to enhance performance through learned representations or fine-tuning. Ensemble learning techniques combine predictions from multiple models, boosting robustness and accuracy. This research contributes to DNA methylation analysis and lays the groundwork for understanding 4mC's multifaceted role in biological processes. The web server for DeepSF-4mC is accessible at: http://deepsf-4mc.top/and the original code can be found at: https://github.com/754131799/DeepSF-4mC.

Topics & Concepts

InterpretabilityDNA methylationComputer scienceRobustness (evolution)Artificial intelligenceMachine learningDeep learningDNAGeneBiologyGeneticsGene expressionMachine Learning in BioinformaticsGenomics and Phylogenetic StudiesRNA modifications and cancer
DeepSF-4mC: A deep learning model for predicting DNA cytosine 4mC methylation sites leveraging sequence features | Litcius