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Yin, Hongyan

https://orcid.org/0000-0001-9116-5908

Mayo Clinic

Chinese Academy of Sciences

Citations 1

Characterization and identification of long non-coding RNAs based on feature relationship
Wang, Guangyu , Yin, Hongyan , Li, Boyang , Yu, Chunlei , Wang, Fan , Xu, Xingjian , Cao, Jiabao, Bào, Yīmíng , Wang, Liguo , Abbasi, Amir Ali , Bajić, Vladimir B. , Ma, Lina , Zhang, Zhang , Wang, Liguo , Wang, Guangyu , Cao, Jiabao

Bioinformatics | January 8, 2019 | Volume: 35 | Issue: 17 | Pages: 2949-2956

10.1093/bioinformatics/btz008 Get It

Abstract Motivation The significance of long non-coding RNAs (lncRNAs) in many biological processes and diseases has gained intense interests over the past several years. However, computational identification of lncRNAs in a wide range of species remains challenging; it requires prior knowledge of well-established sequences and annotations or species-specific training data, but the reality is that only a limited number of species have high-quality sequences and annotations. Results Here we first characterize lncRNAs in contrast to protein-coding RNAs based on feature relationship and find that the feature relationship between open reading frame length and guanine-cytosine (GC) content presents universally substantial divergence in lncRNAs and protein-coding RNAs, as observed in a broad variety of species. Based on the feature relationship, accordingly, we further present LGC, a novel algorithm for identifying lncRNAs that is able to accurately distinguish lncRNAs from protein-coding RNAs in a cross-species manner without any prior knowledge. As validated on large-scale empirical datasets, comparative results show that LGC outperforms existing algorithms by achieving higher accuracy, well-balanced sensitivity and specificity, and is robustly effective (>90% accuracy) in discriminating lncRNAs from protein-coding RNAs across diverse species that range from plants to mammals. To our knowledge, this study, for the first time, differentially characterizes lncRNAs and protein-coding RNAs based on feature relationship, which is further applied in computational identification of lncRNAs. Taken together, our study represents a significant advance in characterization and identification of lncRNAs and LGC thus bears broad potential utility for computational analysis of lncRNAs in a wide range of species. Availability and implementation LGC web server is publicly available at http://bigd.big.ac.cn/lgc/calculator. The scripts and data can be downloaded at http://bigd.big.ac.cn/biocode/tools/BT000004. Supplementary information Supplementary data are available at Bioinformatics online.