4.6 Article

Differential methods for assessing sensitivity in biological models

Journal

PLOS COMPUTATIONAL BIOLOGY
Volume 18, Issue 6, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pcbi.1009598

Keywords

-

Funding

  1. NIH [T32HG002536]
  2. USPHS [HG006139, GMS141798]
  3. National Science Foundation [OAC-1835443, SII2029670, ECCS-2029670, OAC2103804, PHY-2021825]
  4. U.S. Agency for International Development through Penn State [S002283-USAID]
  5. Advanced Research Projects Agency-Energy (ARPA-E), U.S. Department of Energy [DE-AR0001211, DE-AR0001222]
  6. Research Council of Norway [308817]
  7. United States Air Force Research Laboratory
  8. U.S. Air Force Artificial Intelligence Accelerator [FA8750-192-1000]

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Differential sensitivity analysis is crucial in parameter fitting, uncertainty understanding, and result forecasting. This paper introduces various differential sensitivity methods and evaluates their value in typical biological models. Through case studies, it demonstrates the advantages of differential sensitivity analysis over traditional methods and compares the speed, accuracy, and ease of use of different methods. The forward mode automatic differentiation is found to have the fastest computational time, while the complex perturbation method is the simplest and most generalizable.
Differential sensitivity analysis is indispensable in fitting parameters, understanding uncertainty, and forecasting the results of both thought and lab experiments. Although there are many methods currently available for performing differential sensitivity analysis of biological models, it can be difficult to determine which method is best suited for a particular model. In this paper, we explain a variety of differential sensitivity methods and assess their value in some typical biological models. First, we explain the mathematical basis for three numerical methods: adjoint sensitivity analysis, complex perturbation sensitivity analysis, and forward mode sensitivity analysis. We then carry out four instructive case studies. (a) The CARRGO model for tumor-immune interaction highlights the additional information that differential sensitivity analysis provides beyond traditional naive sensitivity methods, (b) the deterministic SIR model demonstrates the value of using second-order sensitivity in refining model predictions, (c) the stochastic SIR model shows how differential sensitivity can be attacked in stochastic modeling, and (d) a discrete birth-death-migration model illustrates how the complex perturbation method of differential sensitivity can be generalized to a broader range of biological models. Finally, we compare the speed, accuracy, and ease of use of these methods. We find that forward mode automatic differentiation has the quickest computational time, while the complex perturbation method is the simplest to implement and the most generalizable. Author summary Over the past few decades, mathematical modeling has become an indispensable tool in the biologist's toolbox. From deterministic to stochastic to statistical models, computational modeling is ubiquitous in almost every field of biology. Because model parameter estimates are often noisy or depend on poorly understood interactions, it is crucial to examine how both quantitative and qualitative predictions change as parameter estimates change, especially as the number of parameters increases. Sensitivity analysis is the process of understanding how a model's behavior depends on parameter values. Sensitivity analysis simultaneously quantifies prediction certainty and clarifies the underlying biological mechanisms that drive computational models. While sensitivity analysis is universally recognized to be an important step in modeling, it is often unclear how to best leverage the available differential sensitivity methods. In this manuscript we explain and compare various differential sensitivity methods in the hope that best practices will be widely adopted. We stress the relative advantages of existing software and their limitations. We also present a new numerical technique for computing differential sensitivity.

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