Metapath-Based Deep Convolutional Neural Network for Predicting miRNA-Target Association on Heterogeneous Network

被引:4
|
作者
Luo, Jiawei [1 ]
Bao, Yaoting [1 ]
Chen, Xiangtao [1 ]
Shen, Cong [1 ]
机构
[1] Hunan Univ, Coll Comp Sci & Elect Engn, Changsha 410083, Peoples R China
基金
中国国家自然科学基金;
关键词
miRNA-target gene associations; Network representation; Deep learning; Meta-path; MICRORNA; IDENTIFICATION; SEARCH;
D O I
10.1007/s12539-021-00454-3
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Predicting the interactions between microRNAs (miRNAs) and target genes is of great significance for understanding the regulatory mechanism of miRNA and treating complex diseases. The emergence of large-scale, heterogeneous biological networks has offered unprecedented opportunities for revealing miRNA-associated target genes. However, there are still some limitations about automatically learn the feature information of the network in the existing methods. Since network representation learning can self-adaptively capture structure information of the network, we propose a framework based on heterogeneous network representation, MDCNN (Metapath-Based Deep Convolutional Neural Network), to predict the associations between miRNAs and target genes. MDCNN samples the paths between the node pairs in the form of meta-path based on the heterogeneous information network (HIN) about miRNAs and target genes. Then the node feature and the path feature which is learned by the Deep Convolutional Neural Network (DCNN) are spliced together as the representation of the miRNA-target gene, to predict the miRNA-target gene interactions. The experiment results indicate that the performance of MDCNN outperforms other methods in multiple validation metrics by fivefold cross validation. We set an ablation study to identify the necessity of miRNA similarity and target gene similarity for improving the prediction ability of MDCNN. The case studies on hsa-miR-26b-5p and CDKN1A further demonstrates that MDCNN can successfully predict potential miRNA-target gene interactions. [GRAPHICS] .
引用
收藏
页码:547 / 558
页数:12
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