Issue 8, 2018, Issue in Progress

Prediction of microRNA–disease associations with a Kronecker kernel matrix dimension reduction model

Abstract

Identifying the associations between human diseases and microRNAs is key to understanding pathogenicity mechanisms and important for uncovering novel prognostic markers. To date, a series of computational approaches have been developed for the prediction of disease–microRNA associations. However, these methods remain difficult to perform satisfactorily for diseases with a few known associated microRNAs. This study introduces a novel computational model, namely, the Kronecker kernel matrix dimension reduction (KMDR) model, for identifying potential microRNA–disease associations. This model combines microRNA space and disease space in a larger microRNA–disease space by using the Kronecker product or the Kronecker sum. The predictive performance of our proposed approach was evaluated and validated based on known association datasets. The experimental results show that KMDR achieves reliable prediction with an average AUC of 0.8320 for 22 complex diseases, which indeed outperforms other competitive methods. Moreover, case studies on kidney cancer, breast cancer, and esophageal cancer further demonstrate the applicability of our method in the identification of new disease–microRNA pairs. The source code of KMDR is freely available at https://github.com/ghli16/KMDR.

Graphical abstract: Prediction of microRNA–disease associations with a Kronecker kernel matrix dimension reduction model

Supplementary files

Article information

Article type
Paper
Submitted
16 Nov 2017
Accepted
01 Jan 2018
First published
23 Jan 2018
This article is Open Access
Creative Commons BY license

RSC Adv., 2018,8, 4377-4385

Prediction of microRNA–disease associations with a Kronecker kernel matrix dimension reduction model

G. Li, J. Luo, Q. Xiao, C. Liang and P. Ding, RSC Adv., 2018, 8, 4377 DOI: 10.1039/C7RA12491K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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