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HLPI-Ensemble: Prediction of human lncRNA-protein interactions based on ensemble strategy.

Authors :
Hu, Huan
Zhang, Li
Ai, Haixin
Zhang, Hui
Fan, Yetian
Zhao, Qi
Liu, Hongsheng
Source :
RNA Biology; 2018, Vol. 15 Issue 6, p797-806, 10p
Publication Year :
2018

Abstract

LncRNA plays an important role in many biological and disease progression by binding to related proteins. However, the experimental methods for studying lncRNA-protein interactions are time-consuming and expensive. Although there are a few models designed to predict the interactions of ncRNA-protein, they all have some common drawbacks that limit their predictive performance. In this study, we present a model called HLPI-Ensemble designed specifically for human lncRNA-protein interactions. HLPI-Ensemble adopts the ensemble strategy based on three mainstream machine learning algorithms of Support Vector Machines (SVM), Random Forests (RF) and Extreme Gradient Boosting (XGB) to generate HLPI-SVM Ensemble, HLPI-RF Ensemble and HLPI-XGB Ensemble, respectively. The results of 10-fold cross-validation show that HLPI-SVM Ensemble, HLPI-RF Ensemble and HLPI-XGB Ensemble achieved AUCs of 0.95, 0.96 and 0.96, respectively, in the test dataset. Furthermore, we compared the performance of the HLPI-Ensemble models with the previous models through external validation dataset. The results show that the false positives (FPs) of HLPI-Ensemble models are much lower than that of the previous models, and other evaluation indicators of HLPI-Ensemble models are also higher than those of the previous models. It is further showed that HLPI-Ensemble models are superior in predicting human lncRNA-protein interaction compared with previous models. The HLPI-Ensemble is publicly available at: <ext-link>http://ccsipb.lnu.edu.cn/hlpiensemble/</ext-link>. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15476286
Volume :
15
Issue :
6
Database :
Complementary Index
Journal :
RNA Biology
Publication Type :
Academic Journal
Accession number :
131751715
Full Text :
https://doi.org/10.1080/15476286.2018.1457935