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Collaborative Research: Efficient Methods for Identifiability of Dynamic Models

Collaborative Research: Efficient Methods for Identifiability of Dynamic Models
协作研究:动态模型可识别性的有效方法
批准号:
1853525
负责人:
Nicolette Meshkat
金额:
$6.23万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-07-01 至 2022-06-30

项目摘要

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中文摘要
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英文摘要
The goal of the project is to analyze and improve the calibration of dynamic models developed by researchers in biology and other sciences to model real-world processes. Mathematical models are used broadly across biology to understand mechanisms, make predictions, and guide intervention strategies. To do so, the model parameters often must be calibrated using data; the estimated parameters can have significant implications for reliability of insights generated from the model and data. This raises the important question of whether the calibration process is well posed, i.e. is it possible to uniquely estimate model parameters from a given type or set of data? Identifiability analysis is the study of these issues, and this project will improve and expand the currently available set of algebraic identifiability methods to set them on a firmer theoretical basis and address new types of models used broadly in many biological settings. Beyond academia, the algorithms to be developed will allow researchers to successfully link models and experiments to generate model-based insights that improve real-world treatment strategies. Training will be provided to two Ph.D. students working on research for this project. The training component will also include interdisciplinary course development as well as a conference with tutorial lectures and problem sessions to educate industrial and academic participants in the theory, algorithms, and software developed in this project. This project is supported jointly by the Division of Mathematical Sciences Mathematical Biology and Division of Computing and Communication Foundations Algorithmic Foundations programs.More specifically, the investigators will develop, analyze, and implement symbolic and symbolic-numeric algorithms that perform identifiability analysis of dynamic models (including ordinary differential (ODE), delay, and difference equation models) that appear in biology and other sciences. Using these algorithms, they will also carry out identifiability analysis for a range of models drawn from cellular signaling and physiology applications. The proposed algorithms will be based on differential-difference algebra, which connects to identifiability in the common case of rational ODEs/delay/difference equations by applying differential-difference elimination algorithms to the model equations. Such symbolic methods for ODE models have proven to be productive in the area of parameter identifiability. The proposed methods would allow a large class of models to be analyzed for structural identifiability, allowing one to assess which parameters can be estimated and tailor experiment design to answer the questions of interest for treatment strategies and mechanistic insights. For the first time, rigorously justified and analyzed efficient algorithms will be available for identifiability problems in delay and difference equation models. Certified and more efficient algorithms will appear for global identifiability problems in ODE models. To carry out the proposed research, new advances in the algebraic theory of differential/difference equations will be made.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
期刊论文(2)
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会议论文
DOI: 10.1137/18m1204826
发表时间: 2019-01-01
期刊: SIAM JOURNAL ON APPLIED MATHEMATICS
影响因子: 1.9
作者: [Gross, Elizabeth, Harrington, Heather, Shiu, Anne]
通讯作者: Shiu, Anne
DOI: 10.1007/s00285-020-01477-y
发表时间: 2020-03-02
期刊: JOURNAL OF MATHEMATICAL BIOLOGY
影响因子: 1.9
作者: [Gross, Elizabeth, Harrington, Heather, Shiu, Anne]
通讯作者: Shiu, Anne
国内基金
海外基金
Research on Quantum Field Theory without a Lagrangian Description
  • 批准号:
    24ZR1403900
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    SATOSHI NAWATA
  • 依托单位:
Cell Research
Cell Research
Cell Research (细胞研究)