Long non-coding RNAs and complex diseases: from experimental results to computational models | |
Chen, X (Chen, Xing)[ 1 ]; Yan, CC (Yan, Chenggang Clarence)[ 3 ]; Zhang, X (Zhang, Xu)[ 4 ]; You, ZH (You, Zhu-Hong)[ 2 ] | |
刊名 | BRIEFINGS IN BIOINFORMATICS |
2017 | |
卷号 | 18期号:4页码:558-576 |
关键词 | long non-coding RNA complex disease lncRNA-disease association prediction computational model machine learning biological network |
ISSN号 | 1467-5463 |
DOI | 10.1093/bib/bbx130 |
英文摘要 | A better exploring biological processes, means, and functions demands trusted information about Protein-protein interactions (PPIs). High-throughput technologies have produced a large number of PPIs data for various species, however, they are resource-expensive and often suffer from high error rates. To supplement the limitations of the traditional methods, in this paper, a sequence-based computational method is proposed to insight whether two proteins interact or not. The proposed method divides the novel PPIs prediction process into three stages: first, the position-specific scoring matrices (PSSMs) are produced by incorporating the evolutionary information; second, the 352-dimensional feature vector is constructed for each protein pair; third, effective parameters for the ensemble learning algorithm rotation forest (RF) are selected. In the proposed model, the evolutionary features are extracted from PSSM for each protein without considering any protein annotations. In addition, by using more accurate and diverse classifiers constructed by RF algorithm to avoid yielding coincident errors, one sample incorrectly divided by one classifier will be corrected by another classifier. The proposed method is evaluated in terms of accuracy, precision, sensitivity, and so on using Yeast, Human, and Pylori datasets and finds that its performance is superior to that of the competing methods. Specifically, the average accuracies achieved by the proposed method are 97.06% (Yeast), 98.95% (Human), and 89.69% (H.pylori), which improves the accuracy of PPIs prediction by 0.54%similar to 3.89% (Yeast), 1.29%similar to 3.85% (Human), and 0.22%similar to 4.85% (H.pylori). The experimental results prove that the proposed method is an effective alternative approach for predicting novel PPIs. |
WOS记录号 | WOS:000462706200017 |
内容类型 | 期刊论文 |
源URL | [http://ir.xjipc.cas.cn/handle/365002/5735] |
专题 | 新疆理化技术研究所_多语种信息技术研究室 |
作者单位 | 1.China Univ Min & Technol, Sch Informat & Elect Engn, Xuzhou 221116, Peoples R China 2.China Univ Min & Technol, Sch Comp Sci & Technol, Xuzhou 221116, Peoples R China 3.Hangzhou Dianzi Univ, Inst Informat & Control, Hangzhou, Zhejiang, Peoples R China 4.Shandong Univ, Sch Mech Elect & Informat Engn, Jinan, Peoples R China |
推荐引用方式 GB/T 7714 | Chen, X ,Yan, CC ,Zhang, X ,et al. Long non-coding RNAs and complex diseases: from experimental results to computational models[J]. BRIEFINGS IN BIOINFORMATICS,2017,18(4):558-576. |
APA | Chen, X ,Yan, CC ,Zhang, X ,&You, ZH .(2017).Long non-coding RNAs and complex diseases: from experimental results to computational models.BRIEFINGS IN BIOINFORMATICS,18(4),558-576. |
MLA | Chen, X ,et al."Long non-coding RNAs and complex diseases: from experimental results to computational models".BRIEFINGS IN BIOINFORMATICS 18.4(2017):558-576. |
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