Be-1DCNN: a neural network model for chromatin loop prediction based on bagging ensemble learning.

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Briefings in Functional Genomics Pub Date : 2023-11-10 DOI:10.1093/bfgp/elad015
Hao Wu, Bing Zhou, Haoru Zhou, Pengyu Zhang, Meili Wang
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Abstract

The chromatin loops in the three-dimensional (3D) structure of chromosomes are essential for the regulation of gene expression. Despite the fact that high-throughput chromatin capture techniques can identify the 3D structure of chromosomes, chromatin loop detection utilizing biological experiments is arduous and time-consuming. Therefore, a computational method is required to detect chromatin loops. Deep neural networks can form complex representations of Hi-C data and provide the possibility of processing biological datasets. Therefore, we propose a bagging ensemble one-dimensional convolutional neural network (Be-1DCNN) to detect chromatin loops from genome-wide Hi-C maps. First, to obtain accurate and reliable chromatin loops in genome-wide contact maps, the bagging ensemble learning method is utilized to synthesize the prediction results of multiple 1DCNN models. Second, each 1DCNN model consists of three 1D convolutional layers for extracting high-dimensional features from input samples and one dense layer for producing the prediction results. Finally, the prediction results of Be-1DCNN are compared to those of the existing models. The experimental results indicate that Be-1DCNN predicts high-quality chromatin loops and outperforms the state-of-the-art methods using the same evaluation metrics. The source code of Be-1DCNN is available for free at https://github.com/HaoWuLab-Bioinformatics/Be1DCNN.

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Be-1DCNN:基于bagging集成学习的染色质环预测神经网络模型。
染色体三维(3D)结构中的染色质环对基因表达的调控至关重要。尽管高通量染色质捕获技术可以识别染色体的三维结构,但利用生物学实验进行染色质环检测是艰巨而耗时的。因此,需要一种计算方法来检测染色质环。深度神经网络可以形成Hi-C数据的复杂表示,并提供处理生物数据集的可能性。因此,我们提出了一个bagging ensemble一维卷积神经网络(Be-1DCNN)来检测全基因组Hi-C图谱中的染色质环。首先,为了获得准确可靠的全基因组接触图谱中的染色质环,利用bagging集成学习方法对多个1DCNN模型的预测结果进行综合。其次,每个1DCNN模型由三个用于从输入样本中提取高维特征的1D卷积层和一个用于生成预测结果的致密层组成。最后,将Be-1DCNN的预测结果与现有模型的预测结果进行了比较。实验结果表明,Be-1DCNN预测高质量的染色质环,并且使用相同的评估指标优于最先进的方法。Be-1DCNN的源代码可在https://github.com/HaoWuLab-Bioinformatics/Be1DCNN上免费获得。
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来源期刊
Briefings in Functional Genomics
Briefings in Functional Genomics BIOTECHNOLOGY & APPLIED MICROBIOLOGY-GENETICS & HEREDITY
CiteScore
6.30
自引率
2.50%
发文量
37
审稿时长
6-12 weeks
期刊介绍: Briefings in Functional Genomics publishes high quality peer reviewed articles that focus on the use, development or exploitation of genomic approaches, and their application to all areas of biological research. As well as exploring thematic areas where these techniques and protocols are being used, articles review the impact that these approaches have had, or are likely to have, on their field. Subjects covered by the Journal include but are not restricted to: the identification and functional characterisation of coding and non-coding features in genomes, microarray technologies, gene expression profiling, next generation sequencing, pharmacogenomics, phenomics, SNP technologies, transgenic systems, mutation screens and genotyping. Articles range in scope and depth from the introductory level to specific details of protocols and analyses, encompassing bacterial, fungal, plant, animal and human data. The editorial board welcome the submission of review articles for publication. Essential criteria for the publication of papers is that they do not contain primary data, and that they are high quality, clearly written review articles which provide a balanced, highly informative and up to date perspective to researchers in the field of functional genomics.
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