EPIMR: Prediction of Enhancer-Promoter Interactions by Multi-Scale ResNet on Image Representation

被引:0
|
作者
Meng, Qiaozhen [1 ]
Lyu, Yinuo [2 ]
Peng, Xiaoqing [3 ,4 ]
Xu, Junhai [1 ]
Tang, Jijun [5 ]
Guo, Fei [6 ]
机构
[1] Tianjin Univ, Coll Intelligence & Comp, Sch Comp Sci & Technol, Tianjin 300350, Peoples R China
[2] Aeronaut Informat Serv Ctr Civil Aviat Adm China A, Beijing 100015, Peoples R China
[3] Cent South Univ, Ctr Med Genet, Changsha 410038, Peoples R China
[4] Cent South Univ, Sch Life Sci, Hunan Key Lab Med Genet, Changsha 410038, Peoples R China
[5] Chinese Acad Sci, Shenzhen Inst Adv Technol, Shenzhen 518000, Peoples R China
[6] Cent South Univ, Sch Comp Sci & Engn, Changsha 410083, Peoples R China
来源
BIG DATA MINING AND ANALYTICS | 2024年 / 7卷 / 03期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
enhancer-promoter interactions; Hilbert Curve; multi-scale residual neural network (ResNet); GENOME; ARCHITECTURE; PRINCIPLES; SEQUENCE;
D O I
10.26599/BDMA.2024.9020018
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Prediction of enhancer-promoter interactions (EPIs) is key to regulating gene expression and diagnosing genetic diseases. Due to limited resolution, biological experiments perform not as well as expected while precisely identifying specific interactions, giving rise to computational biology approaches. Many EPI predictors have been developed, but their prediction accuracy still needs to be enhanced. Here, we design a new model named EPIMR to identify enhancer-promoter interactions. First, Hilbert Curve is utilized to represent sequences to images to preserve the position and spatial information. Second, a multi-scale residual neural network (ResNet) is used to learn the distinguishing features of different abstraction levels. Finally, matching heuristics are adopted to concatenate the learned features of enhancers and promoters, which pays attention to their potential interaction information. Experimental results on six cell lines indicate that EPIMR performs better than existing methods, with higher area under the precision-recall curve (AUPR) and area under the receiver operating characteristic (AUROC) results on benchmark and under-sampling datasets. Furthermore, our model is pre-trained on all cell lines, which improves not only the transferability of cross-cell line prediction, but also cell line-specific prediction ability. In conclusion, our method serves as a valuable technical tool for predicting enhancer-promoter interactions, contributing to the understanding of gene transcription mechanisms. Our code and results are available at https://github.com/guofei-tju/EPIMR.
引用
收藏
页码:668 / 681
页数:14
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