Evidence map›Paper›PMID 31547811›Full record

ArticleJournal of translational medicine2019

WBNPMD: weighted bipartite network projection for microRNA-disease association prediction.

Guobo Xie, Zhiliang Fan, Yuping Sun, Cuiming Wu, Lei Ma

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Article in Journal of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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5 citing papers in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Guobo XieSchool of Computer Science, Guangdong University of Technology, Guangzhou, China.
Zhiliang FanSchool of Computer Science, Guangdong University of Technology, Guangzhou, China.
Yuping SunSchool of Computer Science, Guangdong University of Technology, Guangzhou, China. syp@gdut.edu.cn.ORCID 0000-0003-3010-329X
Cuiming WuSchool of Computer Science, Guangdong University of Technology, Guangzhou, China.
Lei MaInstitute of Automation, Chinese Academy of Sciences, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecently, numerous biological experiments have indicated that microRNAs (miRNAs) play critical roles in exploring the pathogenesis of various human diseases. Since traditional experimental methods for miRNA-disease associations detection are costly and time-consuming, it becomes urgent to design efficient and robust computational techniques for identifying undiscovered interactions.

methodsIn this paper, we proposed a computation framework named weighted bipartite network projection for miRNA-disease association prediction (WBNPMD). In this method, transfer weights were constructed by combining the known miRNA and disease similarities, and the initial information was properly configured. Then the two-step bipartite network algorithm was implemented to infer potential miRNA-disease associations.

resultsThe proposed WBNPMD was applied to the known miRNA-disease association data, and leave-one-out cross-validation (LOOCV) and fivefold cross-validation were implemented to evaluate the performance of WBNPMD. As a result, our method achieved the AUCs of 0.9321 and [Formula: see text] in LOOCV and fivefold cross-validation, and outperformed other four state-of-the-art methods. We also carried out two kinds of case studies on prostate neoplasm, colorectal neoplasm, and lung neoplasm, and most of the top 50 predicted miRNAs were confirmed to have an association with the corresponding diseases based on dbDeMC, miR2Disease, and HMDD V3.0 databases.

conclusionsThe experimental results demonstrate that WBNPMD can accurately infer potential miRNA-disease associations. We anticipated that the proposed WBNPMD could serve as a powerful tool for potential miRNA-disease associations excavation.

Indexed as

AlgorithmsGene Regulatory NetworksGenetic Association StudiesArea Under CurveComputational BiologyGenetic Predisposition to DiseaseHumansMicroRNAsROC CurveMicroRNAsBipartite network projectionInitial information configurationmiRNA-disease associationTransfer weight assignment

Identifiers

PMID31547811
PMCPMC6757419

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