Evidence map›Paper›PMID 33054708›Full record

ArticleBMC bioinformatics2020

MCCMF: collaborative matrix factorization based on matrix completion for predicting miRNA-disease associations.

Tian-Ru Wu, Meng-Meng Yin, Cui-Na Jiao, Ying-Lian Gao, Xiang-Zhen Kong, Jin-Xing Liu

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Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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7citing papers in PubMed
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7 citing papers in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Tian-Ru WuSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Meng-Meng YinSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Cui-Na JiaoSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Ying-Lian GaoSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Xiang-Zhen KongSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Jin-Xing LiuSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China. sdcavell@126.com.ORCID http://orcid.org/0000-0001-6104-2149

Funding

National Natural Science Foundation of China 61702299National Natural Science Foundation of China 61872220
6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) are non-coding RNAs with regulatory functions. Many studies have shown that miRNAs are closely associated with human diseases. Among the methods to explore the relationship between the miRNA and the disease, traditional methods are time-consuming and the accuracy needs to be improved. In view of the shortcoming of previous models, a method, collaborative matrix factorization based on matrix completion (MCCMF) is proposed to predict the unknown miRNA-disease associations.

resultsThe complete matrix of the miRNA and the disease is obtained by matrix completion. Moreover, Gaussian Interaction Profile kernel is added to the miRNA functional similarity matrix and the disease semantic similarity matrix. Then the Weight K Nearest Known Neighbors method is used to pretreat the association matrix, so the model is close to the reality. Finally, collaborative matrix factorization method is applied to obtain the prediction results. Therefore, the MCCMF obtains a satisfactory result in the fivefold cross-validation, with an AUC of 0.9569 (0.0005).

conclusionsThe AUC value of MCCMF is higher than other advanced methods in the fivefold cross validation experiment. In order to comprehensively evaluate the performance of MCCMF, accuracy, precision, recall and f-measure are also added. The final experimental results demonstrate that MCCMF outperforms other methods in predicting miRNA-disease associations. In the end, the effectiveness and practicability of MCCMF are further verified by researching three specific diseases.

Indexed as

AlgorithmsGenetic Predisposition to DiseaseArea Under CurveGene Regulatory NetworksHepatoblastomaHumansMicroRNAsReproducibility of ResultsRetinoblastomaRisk FactorsROC CurveMicroRNAsMatrix completionMatrix factorizationMiRNA-disease association predictionWeight K Nearest Known Neighbors

Identifiers

PMID33054708
PMCPMC7556955

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