Computational Models of Infectious Disease Threats

传染病威胁的计算模型

基本信息

项目摘要

DESCRIPTION (provided by applicant): Microbial threats, including bioterrorism and naturally emerging infectious diseases, pose a serious challenge to national security in the United States and to health worldwide. This proposal describes the creation of a center for computational modeling of infectious diseases at the Johns Hopkins Bloomberg School of Public Health, with the collaboration of key experts at the Brookings Institution, the National Aeronautic and Space Administration, the University of Maryland, and Imperial College (London). The overarching aim of this project is to integrate the most advanced and powerful techniques of epidemiological data analysis with those of computer simulation (agent-based modeling) to produce a unified computational epidemiology that is scientifically sound, highly visual and user-friendly, and responsive to biosecurity and public health policy requirements. Data analysis will be guided by the insight that epidemic patterns over space and time can be approached as nearly decomposable systems, in which frequency components of the incidence signal can be isolated and studied. Wavelet transforms, and empiric mode decomposition using Hilbert-Huang Transforms, will be used to sift nonlinear, nonstationary epidemiological data, allowing frequency band patterns to be defined. Isolated frequency modes will then be associated with external forcing (weather, social contact patterns) and internal dynamics (Kermack-McKendrick predator-prey models). Results of the epidemiological data decomposition analysis, along with the knowledge of infectious disease experts, will instruct the creation and development of agent-based models. Such models feature populations of mobile individuals in artificial societies that interact locally with other individuals. Features of the basic model include variable social network structures, individual susceptibility and immunity, incubation periods, transmission rates, contact rates, and other selectable parameters. After the agent-based model is calibrated to generate epidemic patterns consistent with real world epidemiology, preventive strategies including vaccination, contact tracing, isolation, quarantine, and other public health measures will be systematically introduced and their impact evaluated. Methods will be developed for assessing the utility of individual models, and for making decisions based on combined results from more than one model. Infectious diseases to be studied initially include smallpox, SARS, dengue, West Nile, and unknown but hypothetically plausible agents. As part of a Cooperative Agreement, the Center will work with other research groups, a bioinformatics core group, and the NIGMS to develop data sets, software and methods, agent-based models, and visualization tools. In an infectious disease epidemic emergency the Center will redirect its activities to serve the nation's security, as guided by the NIGMS.
描述(由申请人提供):微生物威胁,包括生物恐怖主义和自然出现的传染病,对美国国家安全和全球卫生构成了严重的挑战。 该提案描述了约翰·霍普金斯彭博公共卫生学院的传染病计算模型中心的建立,并在布鲁金斯机构,国家航空航天局,马里兰大学和帝国学院(伦敦)的主要专家合作,国家航空航天和太空管理局的合作。 该项目的总体目的是将流行病学数据分析的最先进,最有力的技术与计算机模拟(基于代理的建模)的技术整合在一起,以生成统一的计算流行病学,该计算流行病学在科学上是合理的,高度的视觉和用户友好的,并且对生物安全和公共卫生政策的响应有反应。 数据分析将以这样的见解为指导,即可以作为几乎可分解的系统接近时间和时间的流行模式,其中可以隔离和研究入射率信号的频率成分。 小波变换和使用Hilbert-huang变换的经验模式分解将用于筛选非线性,非组织的流行病学数据,从而允许定义频段模式。 然后,孤立的频率模式将与外部强迫(天气,社交接触模式)和内部动力学(Kermack-Mckendrick Predator-Prey模型)相关联。 流行病学数据分解分析的结果以及传染病专家的知识将指导基于代理的模型的创建和开发。 这样的模型以人工社会中的流动人群人群为特色,这些人工社会与其他人在本地互动。 基本模型的特征包括可变的社交网络结构,个人敏感性和免疫力,孵化期,传输率,接触率和其他可选参数。 在对基于代理的模型进行校准以产生与现实世界流行病学一致的流行病模式之后,将系统地介绍包括疫苗接种,接触跟踪,隔离,隔离,隔离和其他公共卫生措施在内的预防性策略及其影响。 将开发方法来评估单个模型的实用性,并根据多个模型的综合结果做出决策。 最初要研究的传染病包括天花,SARS,登革热,西尼罗河以及未知但假设合理的药物。 作为合作协议的一部分,该中心将与其他研究小组,生物信息学核心小组以及开发数据集,软件和方法,基于代理的模型和可视化工具的NIGMS合作。 在传染病流行紧急情况下,该中心将重新定向其活动以服务于国家安全的活动,并在Nigms的指导下。

项目成果

期刊论文数量(26)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Antiviral medications for pregnant women for pandemic and seasonal influenza: an economic computer model.
  • DOI:
    10.1097/aog.0b013e3181bdbfed
  • 发表时间:
    2009-11
  • 期刊:
  • 影响因子:
    7.2
  • 作者:
    Lee BY;Bailey RR;Wiringa AE;Assi TM;Beigi RH
  • 通讯作者:
    Beigi RH
The impact of heterogeneous transmission on the establishment and spread of antimalarial drug resistance.
  • DOI:
    10.1016/j.jtbi.2013.09.022
  • 发表时间:
    2014-01-07
  • 期刊:
  • 影响因子:
    2
  • 作者:
    Klein, Eili Y.
  • 通讯作者:
    Klein, Eili Y.
The potential economic value of a Staphylococcus aureus vaccine for neonates.
新生儿金黄色葡萄球菌疫苗的潜在经济价值。
  • DOI:
    10.1016/j.vaccine.2010.04.069
  • 发表时间:
    2010
  • 期刊:
  • 影响因子:
    5.5
  • 作者:
    Lee,BruceY;Ufberg,PaulJ;Bailey,RachelR;Wiringa,AnnE;Smith,KennethJ;Nowalk,AndrewJ;Higgins,Conor;Wateska,AngelaR;Muder,RobertR
  • 通讯作者:
    Muder,RobertR
Hospital-community interactions foster coexistence between methicillin-resistant strains of Staphylococcus aureus.
  • DOI:
    10.1371/journal.ppat.1003134
  • 发表时间:
    2013-02
  • 期刊:
  • 影响因子:
    6.7
  • 作者:
    Kouyos R;Klein E;Grenfell B
  • 通讯作者:
    Grenfell B
Local spatial and temporal processes of influenza in Pennsylvania, USA: 2003-2009.
  • DOI:
    10.1371/journal.pone.0034245
  • 发表时间:
    2012
  • 期刊:
  • 影响因子:
    3.7
  • 作者:
    Stark JH;Sharma R;Ostroff S;Cummings DA;Ermentrout B;Stebbins S;Burke DS;Wisniewski SR
  • 通讯作者:
    Wisniewski SR
{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

DONALD SCOTT BURKE其他文献

DONALD SCOTT BURKE的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('DONALD SCOTT BURKE', 18)}}的其他基金

Development of a Novel, Sensitive ZIKV-Specific Sero-diagnostic Assay Utilizing Biologically Inspired Synthetic Molecules
利用受生物学启发的合成分子开发新型、灵敏的 ZIKV 特异性血清诊断检测方法
  • 批准号:
    9215750
  • 财政年份:
    2016
  • 资助金额:
    $ 5.83万
  • 项目类别:
Computational Models of Infectious Disease Threats
传染病威胁的计算模型
  • 批准号:
    8513350
  • 财政年份:
    2009
  • 资助金额:
    $ 5.83万
  • 项目类别:
Computational Models of Infectious Disease Threats
传染病威胁的计算模型
  • 批准号:
    8291264
  • 财政年份:
    2009
  • 资助金额:
    $ 5.83万
  • 项目类别:
Computational Models of Infectious Disease Threats
传染病威胁的计算模型
  • 批准号:
    8126337
  • 财政年份:
    2009
  • 资助金额:
    $ 5.83万
  • 项目类别:
Center for Immunology of Emerging Infectious Diseases
新发传染病免疫学中心
  • 批准号:
    7936201
  • 财政年份:
    2009
  • 资助金额:
    $ 5.83万
  • 项目类别:
Computational Models of Infectious Disease Threats
传染病威胁的计算模型
  • 批准号:
    8757566
  • 财政年份:
    2009
  • 资助金额:
    $ 5.83万
  • 项目类别:
Computational Models of Infectious Disease Threats
传染病威胁的计算模型
  • 批准号:
    7908072
  • 财政年份:
    2009
  • 资助金额:
    $ 5.83万
  • 项目类别:
Computational Models of Infectious Disease Threats
传染病威胁的计算模型
  • 批准号:
    9515001
  • 财政年份:
    2009
  • 资助金额:
    $ 5.83万
  • 项目类别:
Center for Immunology of Emerging Infectious Diseases
新发传染病免疫学中心
  • 批准号:
    7663373
  • 财政年份:
    2009
  • 资助金额:
    $ 5.83万
  • 项目类别:
Computational Models of Infectious Disease Threats
传染病威胁的计算模型
  • 批准号:
    7908082
  • 财政年份:
    2009
  • 资助金额:
    $ 5.83万
  • 项目类别:

相似海外基金

Children's National Hospital Site Consortium - Adolescent Medicine Trials Network for HIV/AIDS Interventions (ATN) Operations and Collaborations Center (UM2 Clinical Trial Optional)
国家儿童医院基地联盟 - HIV/艾滋病干预青少年医学试验网络 (ATN) 运营和合作中心(UM2 临床试验可选)
  • 批准号:
    10599559
  • 财政年份:
    2022
  • 资助金额:
    $ 5.83万
  • 项目类别:
A technology-based psychosocial intervention to support social engagement and well-being in adults aging with HIV
基于技术的社会心理干预,支持艾滋病毒感染者的社会参与和福祉
  • 批准号:
    10481052
  • 财政年份:
    2022
  • 资助金额:
    $ 5.83万
  • 项目类别:
A Gene Drive Therapy for HIV: single-administration intervention for high-risk groups
HIV基因驱动疗法:针对高危人群的单次给药干预
  • 批准号:
    10404422
  • 财政年份:
    2021
  • 资助金额:
    $ 5.83万
  • 项目类别:
A Gene Drive Therapy for HIV: single-administration intervention for high-risk groups
HIV基因驱动疗法:针对高危人群的单次给药干预
  • 批准号:
    10597282
  • 财政年份:
    2020
  • 资助金额:
    $ 5.83万
  • 项目类别:
A Gene Drive Therapy for HIV: single-administration intervention for high-risk groups
HIV基因驱动疗法:针对高危人群的单次给药干预
  • 批准号:
    10377987
  • 财政年份:
    2020
  • 资助金额:
    $ 5.83万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了