细胞信号动力学的离散建模工具箱。

IF 1.4 4区 生物学 Q4 CELL BIOLOGY
Yasmin Z Paterson, David Shorthouse, Markus W Pleijzier, Nir Piterman, Claus Bendtsen, Benjamin A Hall, Jasmin Fisher
{"title":"细胞信号动力学的离散建模工具箱。","authors":"Yasmin Z Paterson, David Shorthouse, Markus W Pleijzier, Nir Piterman, Claus Bendtsen, Benjamin A Hall, Jasmin Fisher","doi":"10.1039/c8ib00026c","DOIUrl":null,"url":null,"abstract":"<p><p>In an age where the volume of data regarding biological systems exceeds our ability to analyse it, many researchers are looking towards systems biology and computational modelling to help unravel the complexities of gene and protein regulatory networks. In particular, the use of discrete modelling allows generation of signalling networks in the absence of full quantitative descriptions of systems, which are necessary for ordinary differential equation (ODE) models. In order to make such techniques more accessible to mainstream researchers, tools such as the BioModelAnalyzer (BMA) have been developed to provide a user-friendly graphical interface for discrete modelling of biological systems. Here we use the BMA to build a library of discrete target functions of known canonical molecular interactions, translated from ordinary differential equations (ODEs). We then show that these BMA target functions can be used to reconstruct complex networks, which can correctly predict many known genetic perturbations. This new library supports the accessibility ethos behind the creation of BMA, providing a toolbox for the construction of complex cell signalling models without the need for extensive experience in computer programming or mathematical modelling, and allows for construction and simulation of complex biological systems with only small amounts of quantitative data.</p>","PeriodicalId":80,"journal":{"name":"Integrative Biology","volume":"10 6","pages":"370-382"},"PeriodicalIF":1.4000,"publicationDate":"2018-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A toolbox for discrete modelling of cell signalling dynamics.\",\"authors\":\"Yasmin Z Paterson, David Shorthouse, Markus W Pleijzier, Nir Piterman, Claus Bendtsen, Benjamin A Hall, Jasmin Fisher\",\"doi\":\"10.1039/c8ib00026c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In an age where the volume of data regarding biological systems exceeds our ability to analyse it, many researchers are looking towards systems biology and computational modelling to help unravel the complexities of gene and protein regulatory networks. In particular, the use of discrete modelling allows generation of signalling networks in the absence of full quantitative descriptions of systems, which are necessary for ordinary differential equation (ODE) models. In order to make such techniques more accessible to mainstream researchers, tools such as the BioModelAnalyzer (BMA) have been developed to provide a user-friendly graphical interface for discrete modelling of biological systems. Here we use the BMA to build a library of discrete target functions of known canonical molecular interactions, translated from ordinary differential equations (ODEs). We then show that these BMA target functions can be used to reconstruct complex networks, which can correctly predict many known genetic perturbations. This new library supports the accessibility ethos behind the creation of BMA, providing a toolbox for the construction of complex cell signalling models without the need for extensive experience in computer programming or mathematical modelling, and allows for construction and simulation of complex biological systems with only small amounts of quantitative data.</p>\",\"PeriodicalId\":80,\"journal\":{\"name\":\"Integrative Biology\",\"volume\":\"10 6\",\"pages\":\"370-382\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2018-06-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Integrative Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1039/c8ib00026c\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Integrative Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1039/c8ib00026c","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

在一个关于生物系统的数据量超过我们分析能力的时代,许多研究人员正在寻求系统生物学和计算建模来帮助解开基因和蛋白质调节网络的复杂性。特别是,离散建模的使用允许在没有系统的完整定量描述的情况下生成信号网络,这是常微分方程(ODE)模型所必需的。为了使主流研究人员更容易获得这些技术,已经开发出诸如生物模型分析仪(BMA)之类的工具,为生物系统的离散建模提供用户友好的图形界面。在这里,我们使用BMA建立了一个已知典型分子相互作用的离散目标函数库,这些函数是由常微分方程(ode)转换而来的。然后,我们证明这些BMA目标函数可以用来重建复杂的网络,它可以正确地预测许多已知的遗传扰动。这个新的图书馆支持创建BMA背后的可访问性精神,提供一个工具箱,用于构建复杂的细胞信号模型,而不需要在计算机编程或数学建模方面的丰富经验,并允许构建和模拟复杂的生物系统,只有少量的定量数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A toolbox for discrete modelling of cell signalling dynamics.

In an age where the volume of data regarding biological systems exceeds our ability to analyse it, many researchers are looking towards systems biology and computational modelling to help unravel the complexities of gene and protein regulatory networks. In particular, the use of discrete modelling allows generation of signalling networks in the absence of full quantitative descriptions of systems, which are necessary for ordinary differential equation (ODE) models. In order to make such techniques more accessible to mainstream researchers, tools such as the BioModelAnalyzer (BMA) have been developed to provide a user-friendly graphical interface for discrete modelling of biological systems. Here we use the BMA to build a library of discrete target functions of known canonical molecular interactions, translated from ordinary differential equations (ODEs). We then show that these BMA target functions can be used to reconstruct complex networks, which can correctly predict many known genetic perturbations. This new library supports the accessibility ethos behind the creation of BMA, providing a toolbox for the construction of complex cell signalling models without the need for extensive experience in computer programming or mathematical modelling, and allows for construction and simulation of complex biological systems with only small amounts of quantitative data.

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
Integrative Biology
Integrative Biology 生物-细胞生物学
CiteScore
4.90
自引率
0.00%
发文量
15
审稿时长
1 months
期刊介绍: Integrative Biology publishes original biological research based on innovative experimental and theoretical methodologies that answer biological questions. The journal is multi- and inter-disciplinary, calling upon expertise and technologies from the physical sciences, engineering, computation, imaging, and mathematics to address critical questions in biological systems. Research using experimental or computational quantitative technologies to characterise biological systems at the molecular, cellular, tissue and population levels is welcomed. Of particular interest are submissions contributing to quantitative understanding of how component properties at one level in the dimensional scale (nano to micro) determine system behaviour at a higher level of complexity. Studies of synthetic systems, whether used to elucidate fundamental principles of biological function or as the basis for novel applications are also of interest.
×
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:604180095
Book学术官方微信