EPIP: a novel approach for condition-specific enhancer-promoter interaction prediction

被引:26
|
作者
Talukder, Amlan [1 ]
Saadat, Samaneh [1 ]
Li, Xiaoman [2 ]
Hu, Haiyan [1 ]
机构
[1] Univ Cent Florida, Dept Comp Sci, Orlando, FL 32816 USA
[2] Univ Cent Orlando, Coll Med, Burnett Sch Biomed Sci, Orlando, FL 32816 USA
基金
美国国家科学基金会;
关键词
HUMAN GENOME; DISCOVERY; REVEALS; MAP;
D O I
10.1093/bioinformatics/btz641
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: The identification of enhancer-promoter interactions (EPIs), especially condition-specific ones, is important for the study of gene transcriptional regulation. Existing experimental approaches for EPI identification are still expensive, and available computational methods either do not consider or have low performance in predicting condition-specific EPIs. Results: We developed a novel computational method called EPIP to reliably predict EPIs, especially condition-specific ones. EPIP is capable of predicting interactions in samples with limited data as well as in samples with abundant data. Tested on more than eight cell lines, EPIP reliably identifies EPIs, with an average area under the receiver operating characteristic curve of 0.95 and an average area under the precision-recall curve of 0.73. Tested on condition-specific EPIPs, EPIP correctly identified 99.26% of them. Compared with two recently developed methods, EPIP outperforms them with a better accuracy.
引用
收藏
页码:3877 / 3883
页数:7
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