Evidence map›Paper›PMID 31568653›Full record

ArticleJournal of cellular and molecular medicine2020

LNRLMI: Linear neighbour representation for predicting lncRNA-miRNA interactions.

Leon Wong, Yu-An Huang, Zhu-Hong You, Zhan-Heng Chen, Mei-Yuan Cao

Abstract read
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Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

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15citing 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

15 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.

Leon WongThe Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, China.ORCID 0000-0002-6864-991X
Yu-An HuangDepartment of Computing, Hong Kong Polytechnic University, Kowloon, Hong Kong.ORCID 0000-0002-5346-2394
Zhu-Hong YouThe Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, China.
Zhan-Heng ChenThe Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, China.
Mei-Yuan CaoGuang Dong Polytechnic College, Zhaoqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LncRNA and miRNA are key molecules in mechanism of competing endogenous RNAs(ceRNA), and their interactions have been discovered with important roles in gene regulation. As supplementary to the identification of lncRNA-miRNA interactions from CLIP-seq experiments, in silico prediction can select the most potential candidates for experimental validation. Although developing computational tool for predicting lncRNA-miRNA interaction is of great importance for deciphering the ceRNA mechanism, little effort has been made towards this direction. In this paper, we propose an approach based on linear neighbour representation to predict lncRNA-miRNA interactions (LNRLMI). Specifically, we first constructed a bipartite network by combining the known interaction network and similarities based on expression profiles of lncRNAs and miRNAs. Based on such a data integration, linear neighbour representation method was introduced to construct a prediction model. To evaluate the prediction performance of the proposed model, k-fold cross validations were implemented. As a result, LNRLMI yielded the average AUCs of 0.8475 ± 0.0032, 0.8960 ± 0.0015 and 0.9069 ± 0.0014 on 2-fold, 5-fold and 10-fold cross validation, respectively. A series of comparison experiments with other methods were also conducted, and the results showed that our method was feasible and effective to predict lncRNA-miRNA interactions via a combination of different types of useful side information. It is anticipated that LNRLMI could be a useful tool for predicting non-coding RNA regulation network that lncRNA and miRNA are involved in.

Indexed as

AlgorithmsGene Expression RegulationGene Regulatory NetworksArea Under CurveComputational BiologyGene Expression ProfilingHumansMicroRNAsRNA, Long NoncodingRNA, MessengerMicroRNAsRNA, Long NoncodingRNA, MessengerceRNA networkexpression profilelink predictionlncRNA-miRNA interaction

Identifiers

PMID31568653
PMCPMC6933323

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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.