Evidence map›Paper›PMID 31865912›Full record

ArticleBMC medical genomics2019

MiRNA-disease interaction prediction based on kernel neighborhood similarity and multi-network bidirectional propagation.

Yingjun Ma, Tingting He, Leixin Ge, Chenhao Zhang, Xingpeng Jiang

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Article in BMC medical genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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6citing papers in PubMed
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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yingjun MaSchool of Mathematics & Statistics, Central China Normal University, Wuhan, 430079, Hubei, China.
Tingting HeSchool of Computer, Central China Normal University, Wuhan, 430079, Hubei, China.
Leixin GeSchool of Life Sciences, Central China Normal University, Wuhan, 430079, Hubei, China.
Chenhao ZhangSchool of Computer, Central China Normal University, Wuhan, 430079, Hubei, China.
Xingpeng JiangSchool of Computer, Central China Normal University, Wuhan, 430079, Hubei, China. xpjiang@mail.ccnu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStudies have shown that miRNAs are functionally associated with the development of many human diseases, but the roles of miRNAs in diseases and their underlying molecular mechanisms have not been fully understood. The research on miRNA-disease interaction has received more and more attention. Compared with the complexity and high cost of biological experiments, computational methods can rapidly and efficiently predict the potential miRNA-disease interaction and can be used as a beneficial supplement to experimental methods.

resultsIn this paper, we proposed a novel computational model of kernel neighborhood similarity and multi-network bidirectional propagation (KNMBP) for miRNA-disease interaction prediction, especially for new miRNAs and new diseases. First, we integrated multiple data sources of diseases and miRNAs, respectively, to construct a novel disease semantic similarity network and miRNA functional similarity network. Secondly, based on the modified miRNA-disease interactions, we use the kernel neighborhood similarity algorithm to calculate the disease kernel neighborhood similarity and the miRNA kernel neighborhood similarity. Finally, we utilize bidirectional propagation algorithm to predict the miRNA-disease interaction scores based on the integrated disease similarity network and miRNA similarity network. As a result, the AUC value of 5-fold cross validation for all interactions by KNMBP is 0.93126 based on the commonly used dataset, and the AUC values for all interactions, for all miRNAs, for all disease is 0.93795、0.86363、0.86937 based on another dataset extracted by ourselves, which are higher than other state-of-the-art methods. In addition, our model has good parameter robustness. The case study further demonstrated the predictive performance of the model for novel miRNA-disease interactions.

conclusionsOur KNMBP algorithm efficiently integrates multiple omics data from miRNAs and diseases to stably and efficiently predict potential miRNA-disease interactions. It is anticipated that KNMBP would be a useful tool in biomedical research.

Indexed as

AlgorithmsComputational BiologyDiseaseHumansMicroRNAsNormal DistributionMicroRNAsBidirectional propagationDiffusion component analysisHeterogeneous omics dataKernel neighborhood similarityMicroRNA-disease interaction

Identifiers

PMID31865912
PMCPMC6927119

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.