Benchmark of computational methods for predicting microRNA-disease associations

被引:37
|
作者
Huang, Zhou [1 ]
Liu, Leibo [2 ]
Gao, Yuanxu [1 ]
Shi, Jiangcheng [1 ]
Cui, Qinghua [1 ,3 ]
Li, Jianwei [2 ]
Zhou, Yuan [1 ]
机构
[1] Peking Univ, Sch Basic Med Sci, Dept Biomed Informat,MOE Key Lab Cardiovasc Sci, Dept Physiol & Pathophysiol,Ctr Noncoding RNA Med, 38 Xueyuan Rd, Beijing 100191, Peoples R China
[2] Hebei Univ Technol, Sch Artificial Intelligence, Inst Computat Med, Tianjin 300401, Peoples R China
[3] Univ Elect Sci & Technol China, Sch Life Sci & Technol, Minist Educ, Ctr Bioinformat,Key Lab NeuroInformat, Chengdu 610054, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Benchmarking test; miRNA-disease association; Disease miRNA prediction; DATABASE;
D O I
10.1186/s13059-019-1811-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: A series of miRNA-disease association prediction methods have been proposed to prioritize potential disease-associated miRNAs. Independent benchmarking of these methods is warranted to assess their effectiveness and robustness. Results: Based on more than 8000 novel miRNA-disease associations from the latest HMDD v3.1 database, we perform systematic comparison among 36 readily available prediction methods. Their overall performances are evaluated with rigorous precision-recall curve analysis, where 13 methods show acceptable accuracy (AUPRC > 0.200) while the top two methods achieve a promising AUPRC over 0.300, and most of these methods are also highly ranked when considering only the causal miRNA-disease associations as the positive samples. The potential of performance improvement is demonstrated by combining different predictors or adopting a more updated miRNA similarity matrix, which would result in up to 16% and 46% of AUPRC augmentations compared to the best single predictor and the predictors using the previous similarity matrix, respectively. Our analysis suggests a common issue of the available methods, which is that the prediction results are severely biased toward well-annotated diseases with many associated miRNAs known and cannot further stratify the positive samples by discriminating the causal miRNA-disease associations from the general miRNA-disease associations. Conclusion: Our benchmarking results not only provide a reference for biomedical researchers to choose appropriate miRNA-disease association predictors for their purpose, but also suggest the future directions for the development of more robust miRNA-disease association predictors.
引用
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页数:13
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