Identifying human microRNA-disease associations by a new diffusion-based method

被引:14
作者
Liao, Bo [1 ]
Ding, Sumei [1 ]
Chen, Haowen [1 ]
Li, Zejun [1 ]
Cai, Lijun [1 ]
机构
[1] Hunan Univ, Coll Comp Sci & Elect Engn, Changsha 410082, Hunan, Peoples R China
关键词
MicroRNA-disease association; network similarity; diffusion-based method; GENOME-WIDE ASSOCIATION; BREAST-CANCER; SIMILARITY; DATABASE; GENES; PRIORITIZATION; INTERACTOME; SIGNATURES; TARGETS; MIRNAS;
D O I
10.1142/S0219720015500146
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Identifying the microRNA-disease relationship is vital for investigating the pathogenesis of various diseases. However, experimental verification of disease-related microRNAs remains considerable challenge to many researchers, particularly for the fact that numerous new microRNAs are discovered every year. As such, development of computational methods for disease-related microRNA prediction has recently gained eminent attention. In this paper, first, we construct a miRNA functional network and a disease similarity network by integrating different information sources. Then, we further introduce a new diffusion-based method (NDBM) to explore global network similarity for miRNA-disease association inference. Even though known miRNA-disease associations in the database are rare, NDBM still achieves an area under the ROC curve (AUC) of 85.62% in the leave-one-out cross-validation in improving the prediction accuracy of previous methods significantly. Moreover, our method is applicable to diseases with no known related miRNAs as well as new miRNAs with unknown target diseases. Some associations who strongly predicted by our method are confirmed by public databases. These superior performances suggest that NDBM could be an effective and important tool for biomedical research.
引用
收藏
页数:20
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