DRMDA: deep representations-based miRNA-disease association prediction

被引:67
|
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
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