Abstract

A powerful way of gaining insight into biological systems is by creating a nonlinear differential equation model, which usually contains many unknown parameters. Such a model is called structurally identifiable if it is possible to determine the values of its parameters from measurements of the model outputs. Structural identifiability is a prerequisite for parameter estimation, and should be assessed before exploiting a model. However, this analysis is seldom performed due to the high computational cost involved in the necessary symbolic calculations, which quickly becomes prohibitive as the problem size increases. In this paper we show how to analyse the structural identifiability of a very general class of nonlinear models by extending methods originally developed for studying observability. We present results about models whose identifiability had not been previously determined, report unidentifiabilities that had not been found before, and show how to modify those unidentifiable models to make them identifiable. This method helps prevent problems caused by lack of identifiability analysis, which can compromise the success of tasks such as experiment design, parameter estimation, and model-based optimization. The procedure is called STRIKE-GOLDD (STRuctural Identifiability taKen as Extended-Generalized Observability with Lie Derivatives and Decomposition), and it is implemented in a MATLAB toolbox which is available as open source software. The broad applicability of this approach facilitates the analysis of the increasingly complex models used in systems biology and other areas.

Highlights

  • Mathematical modelling has become a fundamental tool in present day biology [1], and system identification is one of the key tasks of this process [2]

  • Advances in computing power have facilitated the development of increasingly larger dynamic models of biological processes, which usually have many unknown parameters

  • We developed a PLOS Computational Biology | DOI:10.1371/journal.pcbi

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Summary

Introduction

Mathematical modelling has become a fundamental tool in present day biology [1], and system identification is one of the key tasks of this process [2]. While the related concept of practical identifiability refers to quantifying the uncertainty in parameter values when estimated from noisy measurements, structural identifiability does not take into account limitations caused by the quality or availability of experimental data. It is, a necessary (a priori) condition for practical identifiability, which, in turn, is a prerequisite for model calibration, known as parameter estimation [5]. In real applications structural identifiability is seldom checked before performing parameter estimation [9]. This is at least partly due to the computational complexity of the problem: structural identifiability methods generally require symbolic manipulations, which can quickly give rise to long expressions as the system size increases [10]

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