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System Dynamics from Individual Interactions: A process algebra approach to epidemiology

System Dynamics from Individual Interactions: A process algebra approach to epidemiology
个体相互作用的系统动力学:流行病学的过程代数方法
批准号:
EP/E006280/1
负责人:
Carron Shankland
金额:
$43.77万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2007
资助国家:
英国
项目状态:
已结题
起止时间:
2007 至 --

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中文摘要
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英文摘要
Disease can be viewed as a threat or as a tool. Modern society has become vulnerable to wide spreading epidemics, but we also use diseases to control pests in crops as a way of avoiding the use of chemicals. Clearly it is important to be able to understand the way the epidemic works: How much of the population will be infected? Does the behaviour of individuals change the spread of the disease? How long will it take before the disease dies out? What is the most effective way to control the disease?Testing experimentally is not an option: there are ethical problems with infecting people with diseases just to see what happens, therefore we use mathematical models. These help us predict the shape of epidemics and to evaluate methods of control. In this project theoretical computer science techniques known as process algebras will be used to model diseases. The unique benefits of this approach are threefold. Firstly, it is possible to describe the behaviour of individuals directly. Secondly, those individuals can be rigorously combined to give the behaviour of the system as a whole. Thirdly, the system can be formally investigated to establish features of the system dynamics, allowing us to answer the sort of questions posed above. This approach, known as individual-based, is particularly important because in reality we can measure facts about individuals, but our questions about epidemics all come from the population level. The ability to move rigorously between different levels of abstraction (individual to population) when describing disease spread gives us completely new ways of thinking about epidemiology.Our group is the foremost in the world in this work, but we are at the start of a long term research programme. Having built up domain expertise and techniques and tools for describing and investigating simple disease systems in previous work, we are now in a position to consider more complex epidemiological phenomena, the particular modelling features required for these, and further methods of investigation.In this project we will build and investigate process algebra models of specific biological features associated with epidemiology. These are: fluctuating populations (Adding births and deaths), interaction and transmission (If I sneeze on you, will you get my flu? What about the others in the room?), control (How many of the population need to be vaccinated to protect the whole population from the disease?), and contest between individuals (If I don't have enough food will that make me more susceptible to disease?). These features have been chosen as core to the representation of population and epidemiological models and together give a more realistic and rounded model of disease.Exploration of more complex biological systems will require more complex models. Process algebra is expressive enough to describe these systems; however, such descriptions may be clumsy and hard to understand. We will develop new language constructs to allow population models to be more simply expressed, yielding more easily constructed and understood models. Once the model is constructed we have a range of formal techniques to investigate its behaviour, and to compare with other existing models in the literature. We will develop those investigative techniques further, based on the needs of epidemiological systems.Finally, although we will concentrate on epidemiology, the features and techniques developed will be applicable to other areas of biology, and to computer science. For example, instead of viewing an individual as a person or an animal, we could view an individual as a single cell or a complex molecule. In the computer science arena, we can use epidemiological models to think about performance modelling, and also malware (computer viruses, worms etc). This general applicability makes our work particularly exciting.
期刊论文(8)
专著(0)
科研奖励(0)
会议论文
Algebraic Biology
代数生物学
DOI: 10.1007/978-3-540-85101-1_11
发表时间: 2008
期刊:
影响因子: --
作者: [McCaig C]
通讯作者: McCaig C
Using process algebra to develop predator-prey models of within-host parasite dynamics.
使用过程代数开发宿主内寄生虫动力学的捕食者-被捕食者模型。
DOI: 10.1016/j.jtbi.2013.03.001
发表时间: 2013
期刊: Journal of theoretical biology
影响因子: 2
作者: [McCaig C]
通讯作者: McCaig C
FM 2012: Formal Methods - 18th International Symposium, Paris, France, August 27-31, 2012. Proceedings
FM 2012:形式化方法 - 第 18 届国际研讨会,法国巴黎,2012 年 8 月 27-31 日。会议记录
DOI: 10.1007/978-3-642-32759-9_11
发表时间: 2012
期刊:
影响因子: --
作者: [Benkirane S]
通讯作者: Benkirane S
Improving patient outcome by integrating the generic with the personal
  • 批准号:
    EP/K039342/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $156.5万
  • 财政年份:
    2013
  • 负责人:
    Carron Shankland
  • 依托单位:
国内基金
海外基金
β-arrestin2- MFN2-Mitochondrial Dynamics轴调控星形胶质细胞功能对抑郁症进程的影响及机制研究
  • 批准号:
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2023
  • 负责人:
  • 依托单位: