4.5 Article

Adaptive deep propagation graph neural network for predicting miRNA-disease associations

期刊

BRIEFINGS IN FUNCTIONAL GENOMICS
卷 -, 期 -, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bfgp/elad010

关键词

miRNA-disease associations; deep learning; graph neural networks; attention mechanism; heterogeneous graph; propagation

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In this study, a novel miRNA-disease association prediction model (ADPMDA) based on adaptive deep propagation graph neural network is proposed. The miRNA-disease heterogeneous graph is constructed, and the features of miRNAs and diseases are projected into a low-dimensional space. Attention mechanism is used to aggregate local features of central nodes. The effectiveness of ADPMDA is demonstrated through experiments on human miRNA disease database v3.0 dataset.
Background A large number of experiments show that the abnormal expression of miRNA is closely related to the occurrence, diagnosis and treatment of diseases. Identifying associations between miRNAs and diseases is important for clinical applications of complex human diseases. However, traditional biological experimental methods and calculation-based methods have many limitations, which lead to the development of more efficient and accurate deep learning methods for predicting miRNA-disease associations. Results In this paper, we propose a novel model on the basis of adaptive deep propagation graph neural network to predict miRNA-disease associations (ADPMDA). We first construct the miRNA-disease heterogeneous graph based on known miRNA-disease pairs, miRNA integrated similarity information, miRNA sequence information and disease similarity information. Then, we project the features of miRNAs and diseases into a low-dimensional space. After that, attention mechanism is utilized to aggregate the local features of central nodes. In particular, an adaptive deep propagation graph neural network is employed to learn the embedding of nodes, which can adaptively adjust the local and global information of nodes. Finally, the multi-layer perceptron is leveraged to score miRNA-disease pairs. Conclusion Experiments on human microRNA disease database v3.0 dataset show that ADPMDA achieves the mean AUC value of 94.75% under 5-fold cross-validation. We further conduct case studies on the esophageal neoplasm, lung neoplasms and lymphoma to confirm the effectiveness of our proposed model, and 49, 49, 47 of the top 50 predicted miRNAs associated with these diseases are confirmed, respectively. These results demonstrate the effectiveness and superiority of our model in predicting miRNA-disease associations.

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