Evidence map›Paper›PMID 29069317›Full record

ArticleBioinformatics (Oxford, England)2018

Constructing prediction models from expression profiles for large scale lncRNA-miRNA interaction profiling.

Yu-An Huang, Keith C C Chan, Zhu-Hong You

Abstract read
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Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

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49citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

49 citing papers in PubMed.

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  14. PmliHFM: Predicting Plant miRNA-lncRNA Interactions with Hybrid Feature Mining Network.Interdisciplinary sciences, computational life sciences · 2023
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yu-An HuangDepartment of Computing, Hong Kong Polytechnic University, Hong Kong.
Keith C C ChanDepartment of Computing, Hong Kong Polytechnic University, Hong Kong.
Zhu-Hong YouDepartment of Computing, Hong Kong Polytechnic University, Hong Kong.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: The interaction of miRNA and lncRNA is known to be important for gene regulations. However, not many computational approaches have been developed to analyze known interactions and predict the unknown ones. Given that there are now more evidences that suggest that lncRNA-miRNA interactions are closely related to their relative expression levels in the form of a titration mechanism, we analyzed the patterns in large-scale expression profiles of known lncRNA-miRNA interactions. From these uncovered patterns, we noticed that lncRNAs tend to interact collaboratively with miRNAs of similar expression profiles, and vice versa. Results: By representing known interaction between lncRNA and miRNA as a bipartite graph, we propose here a technique, called EPLMI, to construct a prediction model from such a graph. EPLMI performs its tasks based on the assumption that lncRNAs that are highly similar to each other tend to have similar interaction or non-interaction patterns with miRNAs and vice versa. The effectiveness of the prediction model so constructed has been evaluated using the latest dataset of lncRNA-miRNA interactions. The results show that the prediction model can achieve AUCs of 0.8522 and 0.8447 ± 0.0017 based on leave-one-out cross validation and 5-fold cross validation. Using this model, we show that lncRNA-miRNA interactions can be reliably predicted. We also show that we can use it to select the most likely lncRNA targets that specific miRNAs would interact with. We believe that the prediction models discovered by EPLMI can yield great insights for further research on ceRNA regulation network. To the best of our knowledge, EPLMI is the first technique that is developed for large-scale lncRNA-miRNA interaction profiling. Availability and implementation: Matlab codes and dataset are available at https://github.com/yahuang1991polyu/EPLMI/. Contact: yu-an.huang@connect.polyu.hk or zhuhongyou@ms.xjb.ac.cn. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

Gene Expression RegulationAlgorithmsArea Under CurveGene Expression ProfilingHumansMicroRNAsRNA, Long NoncodingSensitivity and SpecificitySequence Analysis, RNAMicroRNAsRNA, Long Noncoding

Identifiers

PMID29069317
PMCPMC6192210

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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.