Gene regulatory network inference based on novel ensemble method.

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Briefings in Functional Genomics Pub Date : 2024-12-06 DOI:10.1093/bfgp/elae036
Bin Yang, Jing Li, Xiang Li, Sanrong Liu
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Abstract

Gene regulatory networks (GRNs) contribute toward understanding the function of genes and the development of cancer or the impact of key genes on diseases. Hence, this study proposes an ensemble method based on 13 basic classification methods and a flexible neural tree (FNT) to improve GRN identification accuracy. The primary classification methods contain ridge classification, stochastic gradient descent, Gaussian process classification, Bernoulli Naive Bayes, adaptive boosting, gradient boosting decision tree, hist gradient boosting classification, eXtreme gradient boosting (XGBoost), multilayer perceptron, light gradient boosting machine, random forest, support vector machine, and k-nearest neighbor algorithm, which are regarded as the input variable set of FNT model. Additionally, a hybrid evolutionary algorithm based on a gene programming variant and particle swarm optimization is developed to search for the optimal FNT model. Experiments on three simulation datasets and three real single-cell RNA-seq datasets demonstrate that the proposed ensemble feature outperforms 13 supervised algorithms, seven unsupervised algorithms (ARACNE, CLR, GENIE3, MRNET, PCACMI, GENECI, and EPCACMI) and four single cell-specific methods (SCODE, BiRGRN, LEAP, and BiGBoost) based on the area under the receiver operating characteristic curve, area under the precision-recall curve, and F1 metrics.

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基于新型集合方法的基因调控网络推断。
基因调控网络(GRN)有助于了解基因的功能、癌症的发展或关键基因对疾病的影响。因此,本研究提出了一种基于 13 种基本分类方法和灵活神经树(FNT)的集合方法,以提高 GRN 识别的准确性。主要分类方法包括脊分类、随机梯度下降、高斯过程分类、伯努利-奈维贝叶斯、自适应提升、梯度提升决策树、直方图梯度提升分类、极端梯度提升(XGBoost)、多层感知器、光梯度提升机、随机森林、支持向量机和 k 近邻算法,这些方法被视为 FNT 模型的输入变量集。此外,还开发了一种基于基因编程变体和粒子群优化的混合进化算法,用于搜索最佳 FNT 模型。在三个模拟数据集和三个真实单细胞RNA-seq数据集上的实验表明,根据接收者操作特征曲线下面积、精度-召回曲线下面积和F1指标,所提出的集合特征优于13种监督算法、7种无监督算法(ARACNE、CLR、GENIE3、MRNET、PCACMI、GENECI和EPCACMI)和4种单细胞特定方法(SCODE、BiRGRN、LEAP和BiGBoost)。
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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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