DRMDA: deep representations-based miRNA-disease association prediction

被引:70
作者
Chen, Xing [1 ]
Gong, Yao [2 ]
Zhang, De-Hong [1 ]
You, Zhu-Hong [3 ]
Li, Zheng-Wei [4 ]
机构
[1] China Univ Min & Technol, Sch Informat & Control Engn, Xuzhou, Peoples R China
[2] Peking Univ, Sch Life Sci, Beijing, Peoples R China
[3] Chinese Acad Sci, Xinjiang Tech Inst Phys & Chem, Urumqi, Peoples R China
[4] China Univ Min & Technol, Sch Comp Sci & Technol, Xuzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
miRNA; disease; miRNA-disease association; deep representation; auto-encoder; HUMAN MICRORNA; FUNCTIONAL SIMILARITY; CANCER; TARGETS; DIAGNOSIS; LYMPHOMA; SCORE; RNAS;
D O I
10.1111/jcmm.13336
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recently, microRNAs (miRNAs) are confirmed to be important molecules within many crucial biological processes and therefore related to various complex human diseases. However, previous methods of predicting miRNA-disease associations have their own deficiencies. Under this circumstance, we developed a prediction method called deep representations-based miRNA-disease association (DRMDA) prediction. The original miRNA-disease association data were extracted from HDMM database. Meanwhile, stacked auto-encoder, greedy layer-wise unsupervised pre-training algorithm and support vector machine were implemented to predict potential associations. We compared DRMDA with five previous classical prediction models (HGIMDA, RLSMDA, HDMP, WBSMDA and RWRMDA) in global leave-one-out cross-validation (LOOCV), local LOOCV and fivefold cross-validation, respectively. The AUCs achieved by DRMDA were 0.9177, 08339 and 0.9156 +/- 0.0006 in the three tests above, respectively. In further case studies, we predicted the top 50 potential miRNAs for colon neoplasms, lymphoma and prostate neoplasms, and 88%, 90% and 86% of the predicted miRNA can be verified by experimental evidence, respectively. In conclusion, DRMDA is a promising prediction method which could identify potential and novel miRNA-disease associations.
引用
收藏
页码:472 / 485
页数:14
相关论文
共 48 条
[1]   microRNAs: Tiny regulators with great potential [J].
Ambros, V .
CELL, 2001, 107 (07) :823-826
[2]  
Bandyopadhyay Sanghamitra, 2010, Silence, V1, P6, DOI 10.1186/1758-907X-1-6
[3]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[4]  
Bengio Y., 2006, ADV NEURAL INFORM PR, V19
[5]   MicroRNA-200 is commonly repressed in conjunctival MALT lymphoma, and targets cyclin E2 [J].
Cai, Jiping ;
Liu, Xiaoyu ;
Cheng, Jinwei ;
Li, You ;
Huang, Xiao ;
Li, Yuzhen ;
Ma, Xiaoye ;
Yu, Hongyu ;
Liu, Huimin ;
Wei, Ruili .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2012, 250 (04) :523-531
[6]   LIBSVM: A Library for Support Vector Machines [J].
Chang, Chih-Chung ;
Lin, Chih-Jen .
ACM TRANSACTIONS ON INTELLIGENT SYSTEMS AND TECHNOLOGY, 2011, 2 (03)
[7]   Long non-coding RNAs and complex diseases: from experimental results to computational models [J].
Chen, Xing ;
Yan, Chenggang Clarence ;
Zhang, Xu ;
You, Zhu-Hong .
BRIEFINGS IN BIOINFORMATICS, 2017, 18 (04) :558-576
[8]   A novel approach based on KATZ measure to predict associations of human microbiota with non-infectious diseases [J].
Chen, Xing ;
Huang, Yu-An ;
You, Zhu-Hong ;
Yan, Gui-Ying ;
Wang, Xue-Song .
BIOINFORMATICS, 2017, 33 (05) :733-739
[9]   FMLNCSIM: fuzzy measure-based lncRNA functional similarity calculation model [J].
Chen, Xing ;
Huang, Yu-An ;
Wang, Xue-Song ;
You, Zhu-Hong ;
Chan, Keith C. C. .
ONCOTARGET, 2016, 7 (29) :45948-45958
[10]   HGIMDA: Heterogeneous graph inference for miRNA-disease association prediction [J].
Chen, Xing ;
Yan, Chenggang Clarence ;
Zhang, Xu ;
You, Zhu-Hong ;
Huang, Yu-An ;
Yan, Gui-Ying .
ONCOTARGET, 2016, 7 (40) :65257-65269