Evidence map›Paper›PMID 27506469›Full record

ArticleBMC genomics2016

IPMiner: hidden ncRNA-protein interaction sequential pattern mining with stacked autoencoder for accurate computational prediction.

Xiaoyong Pan, Yong-Xian Fan, Junchi Yan, Hong-Bin Shen

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Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

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61citing papers in PubMed
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3 · Its place in the literature

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61 citing papers in PubMed.

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  9. Structure-Based Prediction of lncRNA-Protein Interactions by Deep Learning.Methods in molecular biology (Clifton, N.J.) · 2025
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5 · Who and what money

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4 authors.

Xiaoyong PanInstitute of Image Processing and Pattern Recognition, Shanghai Jiao Tong University, and Key Laboratory of System Control and Information Processing, Ministry of Education of China, Dongchuan Road, Shanghai, China.
Yong-Xian FanGuangxi Key Laboratory of Trusted Software, Guangxi Colleges and Universities Key Laboratory of Intelligent Processing of Computer Images and Graphics, Guilin University of Electronic Technology, Guilin, China.
Junchi YanInstitute of Software Engineering, East China Normal University, Shanghai, China.
Hong-Bin ShenInstitute of Image Processing and Pattern Recognition, Shanghai Jiao Tong University, and Key Laboratory of System Control and Information Processing, Ministry of Education of China, Dongchuan Road, Shanghai, China. hbshen@sjtu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-coding RNAs (ncRNAs) play crucial roles in many biological processes, such as post-transcription of gene regulation. ncRNAs mainly function through interaction with RNA binding proteins (RBPs). To understand the function of a ncRNA, a fundamental step is to identify which protein is involved into its interaction. Therefore it is promising to computationally predict RBPs, where the major challenge is that the interaction pattern or motif is difficult to be found.

resultsIn this study, we propose a computational method IPMiner (Interaction Pattern Miner) to predict ncRNA-protein interactions from sequences, which makes use of deep learning and further improves its performance using stacked ensembling. One of the IPMiner's typical merits is that it is able to mine the hidden sequential interaction patterns from sequence composition features of protein and RNA sequences using stacked autoencoder, and then the learned hidden features are fed into random forest models. Finally, stacked ensembling is used to integrate different predictors to further improve the prediction performance. The experimental results indicate that IPMiner achieves superior performance on the tested lncRNA-protein interaction dataset with an accuracy of 0.891, sensitivity of 0.939, specificity of 0.831, precision of 0.945 and Matthews correlation coefficient of 0.784, respectively. We further comprehensively investigate IPMiner on other RNA-protein interaction datasets, which yields better performance than the state-of-the-art methods, and the performance has an increase of over 20 % on some tested benchmarked datasets. In addition, we further apply IPMiner for large-scale prediction of ncRNA-protein network, that achieves promising prediction performance.

conclusionBy integrating deep neural network and stacked ensembling, from simple sequence composition features, IPMiner can automatically learn high-level abstraction features, which had strong discriminant ability for RNA-protein detection. IPMiner achieved high performance on our constructed lncRNA-protein benchmark dataset and other RNA-protein datasets. IPMiner tool is available at http://www.csbio.sjtu.edu.cn/bioinf/IPMiner .

Indexed as

RNA-Binding ProteinsRNA, UntranslatedSoftwareArea Under CurveCluster AnalysisComputational BiologyProtein BindingReproducibility of ResultsRNA-Binding ProteinsRNA, UntranslatedDeep learningncRNAncRNA-proteinStacked ensembing

Identifiers

PMID27506469
PMCPMC4979166

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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.