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Exploiting intrinsic fluctuations to identify model parameters

Parameterisation of kinetic models plays a central role in computational systems biology. Besides the lack of experimental data of high enough quality, some of the biggest challenges here are identification issues. Model parameters can be structurally non‐identifiable because of functional relations...

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Autores principales: Zimmer, Christoph, Sahle, Sven, Pahle, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Institution of Engineering and Technology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687306/
https://www.ncbi.nlm.nih.gov/pubmed/26672148
http://dx.doi.org/10.1049/iet-syb.2014.0010
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author Zimmer, Christoph
Sahle, Sven
Pahle, Jürgen
author_facet Zimmer, Christoph
Sahle, Sven
Pahle, Jürgen
author_sort Zimmer, Christoph
collection PubMed
description Parameterisation of kinetic models plays a central role in computational systems biology. Besides the lack of experimental data of high enough quality, some of the biggest challenges here are identification issues. Model parameters can be structurally non‐identifiable because of functional relationships. Noise in measured data is usually considered to be a nuisance for parameter estimation. However, it turns out that intrinsic fluctuations in particle numbers can make parameters identifiable that were previously non‐identifiable. The authors present a method to identify model parameters that are structurally non‐identifiable in a deterministic framework. The method takes time course recordings of biochemical systems in steady state or transient state as input. Often a functional relationship between parameters presents itself by a one‐dimensional manifold in parameter space containing parameter sets of optimal goodness. Although the system's behaviour cannot be distinguished on this manifold in a deterministic framework it might be distinguishable in a stochastic modelling framework. Their method exploits this by using an objective function that includes a measure for fluctuations in particle numbers. They show on three example models, immigration‐death, gene expression and Epo‐EpoReceptor interaction, that this resolves the non‐identifiability even in the case of measurement noise with known amplitude. The method is applied to partially observed recordings of biochemical systems with measurement noise. It is simple to implement and it is usually very fast to compute. This optimisation can be realised in a classical or Bayesian fashion.
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spelling pubmed-86873062022-02-16 Exploiting intrinsic fluctuations to identify model parameters Zimmer, Christoph Sahle, Sven Pahle, Jürgen IET Syst Biol Article Parameterisation of kinetic models plays a central role in computational systems biology. Besides the lack of experimental data of high enough quality, some of the biggest challenges here are identification issues. Model parameters can be structurally non‐identifiable because of functional relationships. Noise in measured data is usually considered to be a nuisance for parameter estimation. However, it turns out that intrinsic fluctuations in particle numbers can make parameters identifiable that were previously non‐identifiable. The authors present a method to identify model parameters that are structurally non‐identifiable in a deterministic framework. The method takes time course recordings of biochemical systems in steady state or transient state as input. Often a functional relationship between parameters presents itself by a one‐dimensional manifold in parameter space containing parameter sets of optimal goodness. Although the system's behaviour cannot be distinguished on this manifold in a deterministic framework it might be distinguishable in a stochastic modelling framework. Their method exploits this by using an objective function that includes a measure for fluctuations in particle numbers. They show on three example models, immigration‐death, gene expression and Epo‐EpoReceptor interaction, that this resolves the non‐identifiability even in the case of measurement noise with known amplitude. The method is applied to partially observed recordings of biochemical systems with measurement noise. It is simple to implement and it is usually very fast to compute. This optimisation can be realised in a classical or Bayesian fashion. The Institution of Engineering and Technology 2015-04-01 /pmc/articles/PMC8687306/ /pubmed/26672148 http://dx.doi.org/10.1049/iet-syb.2014.0010 Text en © 2020 The Institution of Engineering and Technology https://creativecommons.org/licenses/by/3.0/This is an open access article published by the IET under the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) )
spellingShingle Article
Zimmer, Christoph
Sahle, Sven
Pahle, Jürgen
Exploiting intrinsic fluctuations to identify model parameters
title Exploiting intrinsic fluctuations to identify model parameters
title_full Exploiting intrinsic fluctuations to identify model parameters
title_fullStr Exploiting intrinsic fluctuations to identify model parameters
title_full_unstemmed Exploiting intrinsic fluctuations to identify model parameters
title_short Exploiting intrinsic fluctuations to identify model parameters
title_sort exploiting intrinsic fluctuations to identify model parameters
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687306/
https://www.ncbi.nlm.nih.gov/pubmed/26672148
http://dx.doi.org/10.1049/iet-syb.2014.0010
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