MGCNSS: miRNA-disease association prediction with multi-layer graph convolution and distance-based negative sample selection strategy

被引:0
|
作者
Tian, Zhen [1 ]
Han, Chenguang [2 ]
Xu, Lewen [2 ]
Teng, Zhixia [3 ]
Song, Wei [1 ,2 ]
机构
[1] Zhengzhou Univ, Sch Comp & Artificial Intelligence, Zhengzhou 450000, Peoples R China
[2] Zhengzhou Univ, Zhengzhou, Peoples R China
[3] Northeast Forestry Univ, Coll Informat & Comp Engn, Harbin, Peoples R China
基金
美国国家科学基金会; 国家重点研发计划;
关键词
graph convolutional network; meta-path; distance-based negative sample selection; miRNA-disease association; NETWORK; SIMILARITY; DATABASE;
D O I
10.1093/bib/bbae168
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Identifying disease-associated microRNAs (miRNAs) could help understand the deep mechanism of diseases, which promotes the development of new medicine. Recently, network-based approaches have been widely proposed for inferring the potential associations between miRNAs and diseases. However, these approaches ignore the importance of different relations in meta-paths when learning the embeddings of miRNAs and diseases. Besides, they pay little attention to screening out reliable negative samples which is crucial for improving the prediction accuracy. In this study, we propose a novel approach named MGCNSS with the multi-layer graph convolution and high-quality negative sample selection strategy. Specifically, MGCNSS first constructs a comprehensive heterogeneous network by integrating miRNA and disease similarity networks coupled with their known association relationships. Then, we employ the multi-layer graph convolution to automatically capture the meta-path relations with different lengths in the heterogeneous network and learn the discriminative representations of miRNAs and diseases. After that, MGCNSS establishes a highly reliable negative sample set from the unlabeled sample set with the negative distance-based sample selection strategy. Finally, we train MGCNSS under an unsupervised learning manner and predict the potential associations between miRNAs and diseases. The experimental results fully demonstrate that MGCNSS outperforms all baseline methods on both balanced and imbalanced datasets. More importantly, we conduct case studies on colon neoplasms and esophageal neoplasms, further confirming the ability of MGCNSS to detect potential candidate miRNAs. The source code is publicly available on GitHub https://github.com/15136943622/MGCNSS/tree/master
引用
收藏
页数:17
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