A learning-based framework for miRNA-disease association identification using neural networks

被引:137
作者
Peng, Jiajie [1 ,2 ,3 ]
Hui, Weiwei [1 ]
Li, Qianqian [1 ]
Chen, Bolin [1 ,2 ,3 ]
Hao, Jianye [4 ]
Jiang, Qinghua [5 ]
Shang, Xuequn [1 ,2 ]
Wei, Zhongyu [6 ]
机构
[1] Northwestern Polytech Univ, Sch Comp Sci, Xian 710072, Shaanxi, Peoples R China
[2] Northwestern Polytech Univ, Minist Ind & Informat Technol, Key Lab Big Data Storage & Management, Xian 710072, Shaanxi, Peoples R China
[3] Northwestern Polytech Univ, CMCC, Key Lab Big Data Storage & Management, Xian 710072, Shaanxi, Peoples R China
[4] Tianjin Univ, Coll Intelligence & Comp, Tianjin 300072, Peoples R China
[5] Harbin Inst Technol, Sch Life Sci & Technol, Harbin 150090, Heilongjiang, Peoples R China
[6] Fudan Univ, Sch Data Sci, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
MICRORNAS; SIMILARITY; PREDICTION; DEATH;
D O I
10.1093/bioinformatics/btz254
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: A microRNA (miRNA) is a type of non-coding RNA, which plays important roles in many biological processes. Lots of studies have shown that miRNAs are implicated in human diseases, indicating that miRNAs might be potential biomarkers for various types of diseases. Therefore, it is important to reveal the relationships between miRNAs and diseases/phenotypes. Results: We propose a novel learning-based framework, MDA-CNN, for miRNA-disease association identification. The model first captures interaction features between diseases and miRNAs based on a three-layer network including disease similarity network, miRNA similarity network and protein-protein interaction network. Then, it employs an auto-encoder to identify the essential feature combination for each pair of miRNA and disease automatically. Finally, taking the reduced feature representation as input, it uses a convolutional neural network to predict the final label. The evaluation results show that the proposed framework outperforms some state-of-the-art approaches in a large margin on both tasks of miRNA-disease association prediction and miRNA-phenotype association prediction.
引用
收藏
页码:4364 / 4371
页数:8
相关论文
共 54 条
[1]   MicroRNA pathways in flies and worms: Growth, death, fat, stress, and timing [J].
Ambros, V .
CELL, 2003, 113 (06) :673-676
[2]   Deep learning for computational biology [J].
Angermueller, Christof ;
Parnamaa, Tanel ;
Parts, Leopold ;
Stegle, Oliver .
MOLECULAR SYSTEMS BIOLOGY, 2016, 12 (07)
[3]  
Ardekani Ali M., 2010, Avicenna Journal of Medical Biotechnology, V2, P161
[4]  
Atwood J., 2016, NEURIPS, P2001, DOI DOI 10.5555/3157096.3157320
[5]   miR-15a and miR-16 Are Implicated in Cell Cycle Regulation in a Rb-Dependent Manner and Are Frequently Deleted or Down-regulated in Non-Small Cell Lung Cancer [J].
Bandi, Nora ;
Zbinden, Samuel ;
Gugger, Mathias ;
Arnold, Marlene ;
Kocher, Verena ;
Hasan, Lara ;
Kappeler, Andreas ;
Brunner, Thomas ;
Vassella, Erik .
CANCER RESEARCH, 2009, 69 (13) :5553-5559
[6]  
Baolin L., 2007, NUCLEIC ACIDS RES, V37, pD767
[7]   MicroRNAs and cell cycle regulation [J].
Carleton, Michael ;
Cleary, Michele A. ;
Linsley, Peter S. .
CELL CYCLE, 2007, 6 (17) :2127-2132
[8]   Semi-supervised learning for potential human microRNA-disease associations inference [J].
Chen, Xing ;
Yan, Gui-Ying .
SCIENTIFIC REPORTS, 2014, 4
[9]   RWRMDA: predicting novel human microRNA-disease associations [J].
Chen, Xing ;
Liu, Ming-Xi ;
Yan, Gui-Ying .
MOLECULAR BIOSYSTEMS, 2012, 8 (10) :2792-2798
[10]  
Chicco D., 2014, P ACM BCB 2014 5 ACM, P533