GLNMDA: a novel method for miRNA-disease association prediction based on global linear neighborhoods

RNA Biol. 2018;15(9):1215-1227. doi: 10.1080/15476286.2018.1521210. Epub 2018 Sep 23.

Abstract

Recently, increasing studies have shown that miRNAs are involved in the development and progression of various complex diseases. Consequently, predicting potential miRNA-disease associations makes an important contribution to understanding the pathogenesis of diseases, developing new drugs as well as designing individualized diagnostic and therapeutic approaches for different human diseases. Nonetheless, the inherent noise and incompleteness in the existing biological datasets have limited the prediction accuracy of current computational models. To solve this issue, in this paper, we propose a novel method for miRNA-disease association prediction based on global linear neighborhoods (GLNMDA). Specifically, our method obtains a new miRNA/disease similarity matrix by linearly reconstructing each miRNA/disease according to the known experimentally verified miRNA-disease associations. We then adopt label propagation to infer the potential associations between miRNAs and diseases. As a result, GLNMDA achieved reliable performance in the frameworks of both local and global LOOCV (AUCs of 0.867 and 0.929, respectively) and 5-fold cross validation (average AUC of 0.926). Case studies on five common human diseases further confirmed the utility of our method in discovering latent miRNA-disease pairs. Taken together, GLNMDA could serve as a reliable computational tool for miRNA-disease association prediction.

Keywords: Mirna-disease associations; global linear neighborhoods; label propagation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Area Under Curve
  • Computational Biology / methods*
  • Genetic Predisposition to Disease*
  • Humans
  • MicroRNAs*
  • Models, Genetic
  • Neoplasms / genetics*

Substances

  • MicroRNAs

Grants and funding

CL was supported by the National Natural Science Foundation of China under Grant No. 61602283 and the Natural Science Foundation of Shandong, China, under Grant No.ZR2016FB10. JWL was supported by the National Natural Science Foundation of China under Grant No. 61572180.