Predicting miRNA-disease associations via learning multimodal networks and fusing mixed neighborhood information

被引:65
作者
Lou, Zhengzheng [1 ]
Cheng, Zhaoxu [1 ]
Li, Hui [1 ]
Teng, Zhixia [2 ]
Liu, Yang [3 ]
Tian, Zhen [1 ]
机构
[1] Zhengzhou Univ, Sch Comp & Artificial Intelligence, Zhengzhou 450000, Peoples R China
[2] Northeast Forestry Univ, Coll Informat & Comp Engn, Harbin, Peoples R China
[3] Zhengzhou Univ, Cerebrovasc Dis Dept, Affiliated Hoap 2, Zhengzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
miRNA-disease association; multimodal networks; mixed neighborhood information; Graph Convolutional Network; EXPRESSION PROFILES; PROLIFERATION; DATABASE;
D O I
10.1093/bib/bbac159
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: In recent years, a large number of biological experiments have strongly shown that miRNAs play an important role in understanding disease pathogenesis. The discovery of miRNA-disease associations is beneficial for disease diagnosis and treatment. Since inferring these associations through biological experiments is time-consuming and expensive, researchers have sought to identify the associations utilizing computational approaches. Graph Convolutional Networks (GCNs), which exhibit excellent performance in link prediction problems, have been successfully used in miRNA-disease association prediction. However, GCNs only consider 1st-order neighborhood information at one layer but fail to capture information from high-order neighbors to learn miRNA and disease representations through information propagation. Therefore, how to aggregate information from high-order neighborhood effectively in an explicit way is still challenging. Results: To address such a challenge, we propose a novel method called mixed neighborhood information for miRNA-disease association (MINIMDA), which could fuse mixed high-order neighborhood information of miRNAs and diseases in multimodal networks. First, MINIMDA constructs the integrated miRNA similarity network and integrated disease similarity network respectively with their multisource information. Then, the embedding representations of miRNAs and diseases are obtained by fusing mixed high-order neighborhood information from multimodal network which are the integrated miRNA similarity network, integrated disease similarity network and the miRNA-disease association networks. Finally, we concentrate the multimodal embedding representations of miRNAs and diseases and feed them into the multilayer perceptron (MLP) to predict their underlying associations. Extensive experimental results show that MINIMDA is superior to other state-of-the-art methods overall. Moreover, the outstanding performance on case studies for esophageal cancer, colon tumor and lung cancer further demonstrates the effectiveness of MINIMDA.
引用
收藏
页数:15
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