Prediction of the Association between Transfer RNA and Diseases: A Deep Learning Approach Combining Multi-View Graph Convolution and Attention Mechanisms

计算机科学 图形 人工智能 转移RNA 一般化 相似性(几何) 联想(心理学) 学习迁移 卷积神经网络 数据集 机器学习 计算生物学 数据挖掘 理论计算机科学 核糖核酸 生物 数学 遗传学 数学分析 哲学 认识论 图像(数学) 基因
作者
Xiangkui Li,Dengju Yao,Bo Zhang,Xiaojuan Zhan,Jian Zhang
出处
期刊:ACS omega [American Chemical Society]
卷期号:10 (22): 23808-23816
标识
DOI:10.1021/acsomega.5c03029
摘要

Background: Identifying the associations between transfer RNA (tRNA) and diseases is critical for disease diagnosis and treatment. Computational methods offer an efficient approach for exploring these associations. Methods: We proposed an MGC2ATDA model, which integrated a multiview graph convolutional network, a scaled attention fusion module, and a cross-attention mechanism to identify tRNA-disease associations. First, tRNA sequence data were compiled into the MNDR4.0 data set, and similarity matrices of tRNAs and diseases were integrated separately with the tRNA-disease association network to construct a multiview network. Next, graph convolutional networks were employed to extract node embeddings from the network, which were further integrated via a scaled attention fusion module, generating high-quality node representations. The cross-attention mechanism then refined these representations and achieved tRNA-disease association prediction. Results: On the tRNA-disease association data set, the MGC2ATDA model achieved AUC and AUPR scores of 0.8786 and 0.3657, respectively, outperforming five comparison methods. When applied to the piRNA-disease association data set, the MGC2ATDA model attains AUC and AUPR scores of 0.9353 and 0.6105, demonstrating strong generalization ability. Ablation experiments validated the scaled attention fusion module's effectiveness. Conclusions: As an efficient and accurate computational method, MGC2ATDA provides a critical tool for identifying potential tRNA-disease associations in biomedical research.
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