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.
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Tel Aviv Univ, Blavatnik Sch Comp Sci, IL-69978 Tel Aviv, Israel
Tel Aviv Univ, Sackler Sch Med, Dept Human Mol Genet & Biochem, IL-69978 Tel Aviv, IsraelTel Aviv Univ, Blavatnik Sch Comp Sci, IL-69978 Tel Aviv, Israel
Hait, Tom Aharon
Elkon, Ran
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Tel Aviv Univ, Sackler Sch Med, Dept Human Mol Genet & Biochem, IL-69978 Tel Aviv, Israel
Tel Aviv Univ, Sagol Sch Neurosci, IL-69978 Tel Aviv, IsraelTel Aviv Univ, Blavatnik Sch Comp Sci, IL-69978 Tel Aviv, Israel
Elkon, Ran
Shamir, Ron
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Tel Aviv Univ, Blavatnik Sch Comp Sci, IL-69978 Tel Aviv, IsraelTel Aviv Univ, Blavatnik Sch Comp Sci, IL-69978 Tel Aviv, Israel
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Computational Biology Department, School of Computer Science, Carnegie MellonMachine Learning Department, School of Computer Science, Carnegie Mellon University
Yang Yang
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Barnabs Pczos
Jian Ma
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Computational Biology Department, School of Computer Science, Carnegie MellonMachine Learning Department, School of Computer Science, Carnegie Mellon University