RKNNMDA: Ranking-based KNN for MiRNA-Disease Association prediction

被引:154
|
作者
Chen, Xing [1 ]
Wu, Qiao-Feng [2 ]
Yan, Gui-Ying [3 ]
机构
[1] China Univ Min & Technol, Sch Informat & Control Engn, 1 Daxue Rd, Xuzhou 221116, Jiangsu, Peoples R China
[2] Zhejiang Univ, Coll Elect Engn, Hangzhou, Zhejiang, Peoples R China
[3] Chinese Acad Sci, Acad Math & Syst Sci, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Disease; disease semantic similarity; KNN algorithm; miRNAs; miRNA-disease association; SVM Ranking model; CANCER SYSTEMS BIOLOGY; MICRORNA EXPRESSION; ESOPHAGEAL CANCER; FUNCTIONAL SIMILARITY; REPRESSION; INFERENCE; GENOMICS; FEATURES; DATABASE; GROWTH;
D O I
10.1080/15476286.2017.1312226
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cumulative verified experimental studies have demonstrated that microRNAs (miRNAs) could be closely related with the development and progression of human complex diseases. Based on the assumption that functional similar miRNAs may have a strong correlation with phenotypically similar diseases and vice versa, researchers developed various effective computational models which combine heterogeneous biologic data sets including disease similarity network, miRNA similarity network, and known disease-miRNA association network to identify potential relationships between miRNAs and diseases in biomedical research. Considering the limitations in previous computational study, we introduced a novel computational method of Ranking-based KNN for miRNA-Disease Association prediction (RKNNMDA) to predict potential related miRNAs for diseases, and our method obtained an AUC of 0.8221 based on leave-one-out cross validation. In addition, RKNNMDA was applied to 3 kinds of important human cancers for further performance evaluation. The results showed that 96%, 80% and 94% of predicted top 50 potential related miRNAs for Colon Neoplasms, Esophageal Neoplasms, and Prostate Neoplasms have been confirmed by experimental literatures, respectively. Moreover, RKNNMDA could be used to predict potential miRNAs for diseases without any known miRNAs, and it is anticipated that RKNNMDA would be of great use for novel miRNA-disease association identification.
引用
收藏
页码:952 / 962
页数:11
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