Abstract

BackgroundResearchers discover LncRNA–miRNA regulatory paradigms modulate gene expression patterns and drive major cellular processes. Identification of lncRNA-miRNA interactions (LMIs) is critical to reveal the mechanism of biological processes and complicated diseases. Because conventional wet experiments are time-consuming, labor-intensive and costly, a few computational methods have been proposed to expedite the identification of lncRNA-miRNA interactions. However, little attention has been paid to fully exploit the structural and topological information of the lncRNA-miRNA interaction network.ResultsIn this paper, we propose novel lncRNA-miRNA prediction methods by using graph embedding and ensemble learning. First, we calculate lncRNA-lncRNA sequence similarity and miRNA-miRNA sequence similarity, and then we combine them with the known lncRNA-miRNA interactions to construct a heterogeneous network. Second, we adopt several graph embedding methods to learn embedded representations of lncRNAs and miRNAs from the heterogeneous network, and construct the ensemble models using two ensemble strategies. For the former, we consider individual graph embedding based models as base predictors and integrate their predictions, and develop a method, named GEEL-PI. For the latter, we construct a deep attention neural network (DANN) to integrate various graph embeddings, and present an ensemble method, named GEEL-FI. The experimental results demonstrate both GEEL-PI and GEEL-FI outperform other state-of-the-art methods. The effectiveness of two ensemble strategies is validated by further experiments. Moreover, the case studies show that GEEL-PI and GEEL-FI can find novel lncRNA-miRNA associations.ConclusionThe study reveals that graph embedding and ensemble learning based method is efficient for integrating heterogeneous information derived from lncRNA-miRNA interaction network and can achieve better performance on LMI prediction task. In conclusion, GEEL-PI and GEEL-FI are promising for lncRNA-miRNA interaction prediction.

Highlights

  • Researchers discover LncRNA–miRNA interactions and exploits long non-coding RNA (lncRNA) (miRNA) regulatory paradigms modulate gene expression patterns and drive major cellular processes

  • The following metrics are adopted in our experiments: the area under the precision-recall curve (AUPR), the area under the receiver-operating characteristic curve (AUC), Fmeasure (F1), accuracy (ACC), recall (REC), specificity (SPEC), and precision (PRE)

  • EPLMI and SLNPM are implemented according to the descriptions in the publications, we evaluate the above models on our dataset by using 5-fold cross-validation experiments

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Summary

Introduction

Researchers discover LncRNA–miRNA regulatory paradigms modulate gene expression patterns and drive major cellular processes. Identification of lncRNA-miRNA interactions (LMIs) is critical to reveal the mechanism of biological processes and complicated diseases. MiRNAs are a category of single-stranded, endogenous, evolutionally conserved ncRNAs with 20-25 nt, which are involved in diverse biological processes, such as the regulation of metabolism, cell differentiation, gene expression, embryonic development, and apoptosis [3,4,5]. LncRNAmiRNA regulatory paradigms modulate gene expression patterns that drive major cellular processes (e.g., cell proliferation, cell differentiation, and cell death) which are central to mammalian physiologic and pathologic processes [6]. A critical key to reveal the mechanism of associated biological processes and diseases is to characterize various functions of lncRNAs and miRNAs

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