Exploiting sequence-based features for predicting enhancer-promoter interactions.

TL;DR: This work demonstrates that sequence‐based features alone can reliably predict enhancer‐promoter interactions genome‐wide, which could potentially facilitate the discovery of important sequence determinants for long‐range gene regulation.

Abstract: Motivation A large number of distal enhancers and proximal promoters form enhancer-promoter interactions to regulate target genes in the human genome. Although recent high-throughput genome-wide mapping approaches have allowed us to more comprehensively recognize potential enhancer-promoter interactions, it is still largely unknown whether sequence-based features alone are sufficient to predict such interactions. Results Here, we develop a new computational method (named PEP) to predict enhancer-promoter interactions based on sequence-based features only, when the locations of putative enhancers and promoters in a particular cell type are given. The two modules in PEP (PEP-Motif and PEP-Word) use different but complementary feature extraction strategies to exploit sequence-based information. The results across six different cell types demonstrate that our method is effective in predicting enhancer-promoter interactions as compared to the state-of-the-art methods that use functional genomic signals. Our work demonstrates that sequence-based features alone can reliably predict enhancer-promoter interactions genome-wide, which could potentially facilitate the discovery of important sequence determinants for long-range gene regulation. Availability and implementation The source code of PEP is available at: https://github.com/ma-compbio/PEP . Contact jianma@cs.cmu.edu. Supplementary information Supplementary data are available at Bioinformatics online.