An Efficient Boolean Modelling Approach for Genetic Network Inference

Hasini Nakulugamuwa Gamage, M. Chetty, Adrian B. R. Shatte, J. Hallinan
{"title":"An Efficient Boolean Modelling Approach for Genetic Network Inference","authors":"Hasini Nakulugamuwa Gamage, M. Chetty, Adrian B. R. Shatte, J. Hallinan","doi":"10.1109/CIBCB49929.2021.9562881","DOIUrl":null,"url":null,"abstract":"The inference of Gene Regulatory Networks (GRNs) from time series gene expression data is an effective approach for unveiling important underlying gene-gene relationships and dynamics. While various computational models exist for accurate inference of GRNs, many are computationally inefficient, and do not focus on simultaneous inference of both network topology and dynamics. In this paper, we introduce a simple, Boolean network model-based solution for efficient inference of GRNs. First, the microarray expression data are discretized using the average gene expression value as a threshold. This step permits an experimental approach of defining the maximum indegree of a network. Next, regulatory genes, including the self-regulations for each target gene, are inferred using estimated multivariate mutual information-based Min-Redundancy Max-Relevance Criterion, and further accurate inference is performed by a swapping operation. Subsequently, we introduce a new method, combining Boolean network regulation modelling and Pearson correlation coefficient to identify the interaction types (inhibition or activation) of the regulatory genes. This method is utilized for the efficient determination of the optimal regulatory rule, consisting AND, OR, and NOT operators, by defining the accurate application of the NOT operation in conjunction and disjunction Boolean functions. The proposed approach is evaluated using two real gene expression datasets for an Escherichia coli gene regulatory network and a fission yeast cell cycle network. Although the Structural Accuracy is approximately the same as existing methods (MIBNI, REVEAL, Best-Fit, BIBN, and CST), the proposed method outperforms all these methods with respect to efficiency and Dynamic Accuracy.","PeriodicalId":163387,"journal":{"name":"2021 IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology (CIBCB)","volume":"17 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2021 IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology (CIBCB)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/CIBCB49929.2021.9562881","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7

Abstract

The inference of Gene Regulatory Networks (GRNs) from time series gene expression data is an effective approach for unveiling important underlying gene-gene relationships and dynamics. While various computational models exist for accurate inference of GRNs, many are computationally inefficient, and do not focus on simultaneous inference of both network topology and dynamics. In this paper, we introduce a simple, Boolean network model-based solution for efficient inference of GRNs. First, the microarray expression data are discretized using the average gene expression value as a threshold. This step permits an experimental approach of defining the maximum indegree of a network. Next, regulatory genes, including the self-regulations for each target gene, are inferred using estimated multivariate mutual information-based Min-Redundancy Max-Relevance Criterion, and further accurate inference is performed by a swapping operation. Subsequently, we introduce a new method, combining Boolean network regulation modelling and Pearson correlation coefficient to identify the interaction types (inhibition or activation) of the regulatory genes. This method is utilized for the efficient determination of the optimal regulatory rule, consisting AND, OR, and NOT operators, by defining the accurate application of the NOT operation in conjunction and disjunction Boolean functions. The proposed approach is evaluated using two real gene expression datasets for an Escherichia coli gene regulatory network and a fission yeast cell cycle network. Although the Structural Accuracy is approximately the same as existing methods (MIBNI, REVEAL, Best-Fit, BIBN, and CST), the proposed method outperforms all these methods with respect to efficiency and Dynamic Accuracy.
遗传网络推理的一种高效布尔建模方法
从时间序列基因表达数据推断基因调控网络(GRNs)是揭示重要的潜在基因关系和动态的有效方法。虽然存在各种计算模型来精确推断grn,但许多计算效率低下,并且不关注网络拓扑和动态的同时推断。在本文中,我们介绍了一个简单的,基于布尔网络模型的解决方案,用于grn的有效推理。首先,使用平均基因表达值作为阈值对微阵列表达数据进行离散化。这一步允许用实验方法来定义网络的最大程度。其次,利用估计的多元互信息最小冗余最大相关准则推断调控基因,包括每个目标基因的自我调节,并通过交换操作进行进一步的准确推断。随后,我们引入了一种新的方法,结合布尔网络调控模型和Pearson相关系数来识别调控基因的相互作用类型(抑制或激活)。该方法通过定义NOT运算在合取布尔函数和析取布尔函数中的准确应用,有效地确定由AND、OR和NOT运算符组成的最优调节规则。采用大肠杆菌基因调控网络和裂变酵母细胞周期网络的两个真实基因表达数据集对所提出的方法进行了评估。虽然结构精度与现有方法(MIBNI、REVEAL、Best-Fit、BIBN和CST)大致相同,但该方法在效率和动态精度方面优于所有这些方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信