结合哲加金多项式和 SAT 求解,建立生物系统的特定语境布尔模型

IF 3.6 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS IEEE/ACM Transactions on Computational Biology and Bioinformatics Pub Date : 2024-09-10 DOI:10.1109/TCBB.2024.3456302
Vincent Deman;Marine Ciantar;Laurent Naudin;Philippe Castera;Anne-Sophie Beignon
{"title":"结合哲加金多项式和 SAT 求解,建立生物系统的特定语境布尔模型","authors":"Vincent Deman;Marine Ciantar;Laurent Naudin;Philippe Castera;Anne-Sophie Beignon","doi":"10.1109/TCBB.2024.3456302","DOIUrl":null,"url":null,"abstract":"Large amounts of knowledge regarding biological processes are readily available in the literature and aggregated in diverse databases. Boolean networks are powerful tools to render that knowledge into models that can mimic and simulate biological phenomena at multiple scales. Yet, when a model is required to understand or predict the behavior of a biological system in given conditions, existing information often does not completely match this context. Networks built from only prior knowledge can overlook mechanisms, lack specificity, and just partially recapitulate experimental observations. To address this limitation, context-specific data needs to be integrated. However, the brute-force identification of qualitative rules matching these data becomes infeasible as the number of candidates explodes for increasingly complex systems. Here, we used Zhegalkin polynomials to transform this identification into a binary value assignment for exponentially fewer variables, which we addressed with a state-of-the-art SAT solver. We evaluated our implemented method alongside two widely recognized tools, CellNetOptimizer and Caspo-ts, on both artificial toy models and large-scale models based on experimental data from the HPN-DREAM challenge. Our approach demonstrated benchmark-leading capabilities on networks of significant size and intricate complexity. It thus appears promising for the \n<italic>in silico</i>\n modeling of ever more comprehensive biological systems.","PeriodicalId":13344,"journal":{"name":"IEEE/ACM Transactions on Computational Biology and Bioinformatics","volume":"21 6","pages":"2188-2199"},"PeriodicalIF":3.6000,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10671585","citationCount":"0","resultStr":"{\"title\":\"Combining Zhegalkin Polynomials and SAT Solving for Context-Specific Boolean Modeling of Biological Systems\",\"authors\":\"Vincent Deman;Marine Ciantar;Laurent Naudin;Philippe Castera;Anne-Sophie Beignon\",\"doi\":\"10.1109/TCBB.2024.3456302\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Large amounts of knowledge regarding biological processes are readily available in the literature and aggregated in diverse databases. Boolean networks are powerful tools to render that knowledge into models that can mimic and simulate biological phenomena at multiple scales. Yet, when a model is required to understand or predict the behavior of a biological system in given conditions, existing information often does not completely match this context. Networks built from only prior knowledge can overlook mechanisms, lack specificity, and just partially recapitulate experimental observations. To address this limitation, context-specific data needs to be integrated. However, the brute-force identification of qualitative rules matching these data becomes infeasible as the number of candidates explodes for increasingly complex systems. Here, we used Zhegalkin polynomials to transform this identification into a binary value assignment for exponentially fewer variables, which we addressed with a state-of-the-art SAT solver. We evaluated our implemented method alongside two widely recognized tools, CellNetOptimizer and Caspo-ts, on both artificial toy models and large-scale models based on experimental data from the HPN-DREAM challenge. Our approach demonstrated benchmark-leading capabilities on networks of significant size and intricate complexity. It thus appears promising for the \\n<italic>in silico</i>\\n modeling of ever more comprehensive biological systems.\",\"PeriodicalId\":13344,\"journal\":{\"name\":\"IEEE/ACM Transactions on Computational Biology and Bioinformatics\",\"volume\":\"21 6\",\"pages\":\"2188-2199\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2024-09-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10671585\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IEEE/ACM Transactions on Computational Biology and Bioinformatics\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://ieeexplore.ieee.org/document/10671585/\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE/ACM Transactions on Computational Biology and Bioinformatics","FirstCategoryId":"5","ListUrlMain":"https://ieeexplore.ieee.org/document/10671585/","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

摘要

关于生物过程的大量知识在文献中很容易获得,并汇集在不同的数据库中。布尔网络是将知识转化为模型的强大工具,可以在多个尺度上模拟和模拟生物现象。然而,当需要一个模型来理解或预测给定条件下生物系统的行为时,现有的信息往往不能完全匹配这一背景。仅从先验知识构建的网络可能会忽略机制,缺乏特异性,并且只是部分概括实验观察结果。为了解决这个限制,需要集成特定于上下文的数据。然而,对于日益复杂的系统,随着候选规则数量的爆炸式增长,匹配这些数据的定性规则的暴力识别变得不可行。在这里,我们使用Zhegalkin多项式将这种识别转换为指数较少变量的二进制值赋值,我们使用最先进的SAT求解器来解决这个问题。我们在人工玩具模型和基于HPN-DREAM挑战实验数据的大型模型上,与两种广泛认可的工具CellNetOptimizer和Caspo-ts一起评估了我们的实现方法。我们的方法在规模巨大、复杂的网络上展示了领先基准的能力。因此,它对于更全面的生物系统的计算机建模似乎是有希望的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Combining Zhegalkin Polynomials and SAT Solving for Context-Specific Boolean Modeling of Biological Systems
Large amounts of knowledge regarding biological processes are readily available in the literature and aggregated in diverse databases. Boolean networks are powerful tools to render that knowledge into models that can mimic and simulate biological phenomena at multiple scales. Yet, when a model is required to understand or predict the behavior of a biological system in given conditions, existing information often does not completely match this context. Networks built from only prior knowledge can overlook mechanisms, lack specificity, and just partially recapitulate experimental observations. To address this limitation, context-specific data needs to be integrated. However, the brute-force identification of qualitative rules matching these data becomes infeasible as the number of candidates explodes for increasingly complex systems. Here, we used Zhegalkin polynomials to transform this identification into a binary value assignment for exponentially fewer variables, which we addressed with a state-of-the-art SAT solver. We evaluated our implemented method alongside two widely recognized tools, CellNetOptimizer and Caspo-ts, on both artificial toy models and large-scale models based on experimental data from the HPN-DREAM challenge. Our approach demonstrated benchmark-leading capabilities on networks of significant size and intricate complexity. It thus appears promising for the in silico modeling of ever more comprehensive biological systems.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
7.50
自引率
6.70%
发文量
479
审稿时长
3 months
期刊介绍: IEEE/ACM Transactions on Computational Biology and Bioinformatics emphasizes the algorithmic, mathematical, statistical and computational methods that are central in bioinformatics and computational biology; the development and testing of effective computer programs in bioinformatics; the development of biological databases; and important biological results that are obtained from the use of these methods, programs and databases; the emerging field of Systems Biology, where many forms of data are used to create a computer-based model of a complex biological system
期刊最新文献
Guest Editorial Guest Editorial for the 20th Asia Pacific Bioinformatics Conference iAnOxPep: a machine learning model for the identification of anti-oxidative peptides using ensemble learning. DeepLigType: Predicting Ligand Types of Protein-Ligand Binding Sites Using a Deep Learning Model. Performance Comparison between Deep Neural Network and Machine Learning based Classifiers for Huntington Disease Prediction from Human DNA Sequence. AI-based Computational Methods in Early Drug Discovery and Post Market Drug Assessment: A Survey.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1