Evidence map›Paper›PMID 29943160›Full record

ArticleJournal of cheminformatics2018

Inferring potential small molecule-miRNA association based on triple layer heterogeneous network.

Jia Qu, Xing Chen, Ya-Zhou Sun, Jian-Qiang Li, Zhong Ming

Abstract read
In one paragraph

Article in Journal of cheminformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

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30citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

30 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.

Jia QuSchool of Information and Control Engineering, China University of Mining and Technology, Xuzhou, 221116, China.
Xing ChenSchool of Information and Control Engineering, China University of Mining and Technology, Xuzhou, 221116, China. xingchen@amss.ac.cn.ORCID http://orcid.org/0000-0001-9028-5342
Ya-Zhou SunNational Engineering Laboratory for Big Data System Computing Technology, Shenzhen University, Shenzhen, 518060, China.
Jian-Qiang LiNational Engineering Laboratory for Big Data System Computing Technology, Shenzhen University, Shenzhen, 518060, China.
Zhong MingNational Engineering Laboratory for Big Data System Computing Technology, Shenzhen University, Shenzhen, 518060, China.

Funding

National Natural Science Foundation of China 61772531
6 · The paper itself

Abstract

Recently, many biological experiments have indicated that microRNAs (miRNAs) are a newly discovered small molecule (SM) drug targets that play an important role in the development and progression of human complex diseases. More and more computational models have been developed to identify potential associations between SMs and target miRNAs, which would be a great help for disease therapy and clinical applications for known drugs in the field of medical research. In this study, we proposed a computational model of triple layer heterogeneous network based small molecule-MiRNA association prediction (TLHNSMMA) to uncover potential SM-miRNA associations by integrating integrated SM similarity, integrated miRNA similarity, integrated disease similarity, experimentally verified SM-miRNA associations and miRNA-disease associations into a heterogeneous graph. To evaluate the performance of TLHNSMMA, we implemented global and two types of local leave-one-out cross validation as well as fivefold cross validation to compare TLHNSMMA with one previous classical computational model (SMiR-NBI). As a result, for Dataset 1, TLHNSMMA obtained the AUCs of 0.9859, 0.9845, 0.7645 and 0.9851 ± 0.0012, respectively; for Dataset 2, the AUCs are in turn 0.8149, 0.8244, 0.6057 and 0.8168 ± 0.0022. As the result of case studies shown, among the top 10, 20 and 50 potential SM-related miRNAs, there were 2, 7 and 14 SM-miRNA associations confirmed by experiments, respectively. Therefore, TLHNSMMA could be effectively applied to the prediction of SM-miRNA associations.

Indexed as

Association predictionmicroRNASmall moleculeTriple layer heterogeneous network

Identifiers

PMID29943160
PMCPMC6020102

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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.