GKLOMLI: A link prediction model for inferring miRNA-lncRNA interactions by using Gaussian kernel-based method on network profile and linear optimization algorithm

Author:

Wong Leon1,Wang Lei1,You Zhu-Hong2,Yuan Chang-An1,Huang Yu-An2,Cao Mei-Yuan3

Affiliation:

1. Guangxi Academy of Sciences

2. Northwestern Polytechnical University

3. Guangdong Technology College

Abstract

Abstract Background The limited knowledge of miRNA-lncRNA interactions is considered as an obstruction of revealing the regulatory mechanism. Accumulating evidence on Human diseases indicates that the modulation of gene expression has a great relationship with the interactions between miRNAs and lncRNAs. However, such interaction validation via CLIP-seq experiments inevitably costs too much money and time but with unsatisfactory results. Therefore, more and more computational prediction tools have been developed to offer many reliable candidates for a better design of further bio-experiments. Methods In this work, we proposed a novel link prediction model called GKLOMLI. Given an observed interaction profile without any test sample, the Gaussian kernel-based method was employed to output two similarity matrixes of miRNAs and lncRNAs. Based on the integrated matrix combined with similarity matrixes and the observed interaction network, a linear optimization-based link prediction model was trained for inferring miRNA-lncRNA interactions. Results To evaluate the performance of our proposed method, k-fold cross-validation (CV) and leave-one-out CV were implemented, in which each CV experiment was carried out 100 times on a training set generated randomly. The high AUCs at 0.8623 ± 0.0027 (2-fold CV), 0.9053 ± 0.0017 (5-fold CV), 0.9151 ± 0.0013 (10-fold CV), and 0.9236 (LOO-CV), illustrated the precision and reliability of our proposed method. Conclusion GKLOMLI with high performance is anticipated to be used to reveal underlying interactions between miRNA and their target lncRNAs and decipher the potential mechanisms of the complex diseases.

Publisher

Research Square Platform LLC

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