Multi-Relation Graph Embedding for Predicting miRNA-Target Gene Interactions by Integrating Gene Sequence Information

被引:3
作者
Luo, Jiawei [1 ]
Ouyang, Wenjue [1 ]
Shen, Cong [1 ]
Cai, Jie [1 ]
机构
[1] Hunan Univ, Coll Comp Sci & Elect Engn, Changsha 410000, Peoples R China
基金
中国国家自然科学基金;
关键词
Predictive models; Feature extraction; Convolution; Bioinformatics; Support vector machines; Biological system modeling; Task analysis; Graph embedding; graph convolutional network; heterogeneous information network; miRNA-target gene interactions;
D O I
10.1109/JBHI.2022.3168008
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Accumulated studies have found that miRNAs are in charge of many complex diseases such as cancers by modulating gene expression. Predicting miRNA-target interactions is beneficial for uncovering the crucial roles of miRNAs in regulating target genes and the progression of diseases. The emergence of large-scale genomic and biological data as well as the recent development in heterogeneous networks provides new opportunities for miRNA target identification. Compared with conventional methods, computational methods become a decent solution for high efficiency. Thus, designing a method that could excavate valid information from the heterogeneous network and gene sequences is in great demand for improving the prediction accuracy. In this study, we proposed a graph-based model named MRMTI for the prediction of miRNA-target interactions. MRMTI utilized the multi-relation graph convolution module and the Bi-LSTM module to incorporate both network topology and sequential information. The learned embeddings of miRNAs and genes were then used to calculate the prediction scores of miRNA-target pairs. Comparisons with other state-of-the-art graph embedding methods and existing bioinformatic tools illustrated the superiority of MRMTI under multiple criteria metrics. Three variants of MRMTI implied the positive effect of multi-relation. The experimental results of case studies further demonstrated the prominent ability of MRMTI in predicting novel associations.
引用
收藏
页码:4345 / 4353
页数:9
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