Long non-coding RNAs function annotation: a global prediction method based on bi-colored networks

Xingli Guo(University of Chinese Academy of Sciences), Lin Gao(University of Chinese Academy of Sciences), Qi Liao(University of Chinese Academy of Sciences), Hui Xiao(Institute of Computing Technology), Xiaoke Ma(Institute of Computing Technology), Xiaofei Yang(Binzhou Medical University), Haitao Luo(Binzhou Medical University), Guoguang Zhao(University of Chinese Academy of Sciences), Dechao Bu(Binzhou Medical University), Fei Jiao(Institute of Computing Technology), Qixiang Shao(University of Chinese Academy of Sciences), Runsheng Chen(Institute of Computing Technology), Yi Zhao(University of Chinese Academy of Sciences)
Nucleic Acids Research
November 5, 2012
Cited by 214Open Access
Full Text

Abstract

More and more evidences demonstrate that the long non-coding RNAs (lncRNAs) play many key roles in diverse biological processes. There is a critical need to annotate the functions of increasing available lncRNAs. In this article, we try to apply a global network-based strategy to tackle this issue for the first time. We develop a bi-colored network based global function predictor, long non-coding RNA global function predictor ('lnc-GFP'), to predict probable functions for lncRNAs at large scale by integrating gene expression data and protein interaction data. The performance of lnc-GFP is evaluated on protein-coding and lncRNA genes. Cross-validation tests on protein-coding genes with known function annotations indicate that our method can achieve a precision up to 95%, with a suitable parameter setting. Among the 1713 lncRNAs in the bi-colored network, the 1625 (94.9%) lncRNAs in the maximum connected component are all functionally characterized. For the lncRNAs expressed in mouse embryo stem cells and neuronal cells, the inferred putative functions by our method highly match those in the known literature.


Related Papers

No related papers found

Powered by citation graph analysis