EPIPDLF:用于预测增强子-启动子相互作用的预训练深度学习框架。

Zhichao Xiao, Yan Li, Yijie Ding, Liang Yu
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引用次数: 0

摘要

动机:增强子和启动子作为DNA调控元件,在多种生物过程中的基因表达、体内平衡和疾病发展中起着关键作用。随着研究的深入,已经发现远端增强子可能与附近的启动子结合来调节靶基因的表达。这一发现对加深我们对各种生物机制的理解具有重要意义。近年来,许多高通量湿实验室技术已经创建,以检测增强子和启动子之间可能的相互作用。然而,这些实验方法往往耗时且昂贵。结果:为了解决这个问题,我们创建了一种创新的深度学习方法EPIPDLF,它利用先进的深度学习技术以可解释的方式仅基于基因组序列来预测epi。六个基准数据集的比较评估表明,EPIPDLF在EPI预测中始终表现出卓越的性能。此外,通过结合可解释的分析机制,我们的模型能够阐明学习特征,帮助识别和重要序列的生物学分析。可用性:源代码和数据可从:https://github.com/xzc196/EPIPDLF获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EPIPDLF: a pretrained deep learning framework for predicting enhancer-promoter interactions.

Motivation: Enhancers and promoters, as regulatory DNA elements, play pivotal roles in gene expression, homeostasis, and disease development across various biological processes. With advancing research, it has been uncovered that distal enhancers may engage with nearby promoters to modulate the expression of target genes. This discovery holds significant implications for deepening our comprehension of various biological mechanisms. In recent years, numerous high-throughput wet-lab techniques have been created to detect possible interactions between enhancers and promoters. However, these experimental methods are often time-intensive and costly.

Results: To tackle this issue, we have created an innovative deep learning approach, EPIPDLF, which utilizes advanced deep learning techniques to predict EPIs based solely on genomic sequences in an interpretable manner. Comparative evaluations across six benchmark datasets demonstrate that EPIPDLF consistently exhibits superior performance in EPI prediction. Additionally, by incorporating interpretable analysis mechanisms, our model enables the elucidation of learned features, aiding in the identification and biological analysis of important sequences.

Availability and implementation: The source code and data are available at: https://github.com/xzc196/EPIPDLF.

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