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Practical identifiability in the frame of nonlinear mixed effects models: the example of the in vitro erythropoiesis
BACKGROUND: Nonlinear mixed effects models provide a way to mathematically describe experimental data involving a lot of inter-individual heterogeneity. In order to assess their practical identifiability and estimate confidence intervals for their parameters, most mixed effects modelling programs us...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489053/ https://www.ncbi.nlm.nih.gov/pubmed/34607573 http://dx.doi.org/10.1186/s12859-021-04373-4 |
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author | Duchesne, Ronan Guillemin, Anissa Gandrillon, Olivier Crauste, Fabien |
author_facet | Duchesne, Ronan Guillemin, Anissa Gandrillon, Olivier Crauste, Fabien |
author_sort | Duchesne, Ronan |
collection | PubMed |
description | BACKGROUND: Nonlinear mixed effects models provide a way to mathematically describe experimental data involving a lot of inter-individual heterogeneity. In order to assess their practical identifiability and estimate confidence intervals for their parameters, most mixed effects modelling programs use the Fisher Information Matrix. However, in complex nonlinear models, this approach can mask practical unidentifiabilities. RESULTS: Herein we rather propose a multistart approach, and use it to simplify our model by reducing the number of its parameters, in order to make it identifiable. Our model describes several cell populations involved in the in vitro differentiation of chicken erythroid progenitors grown in the same environment. Inter-individual variability observed in cell population counts is explained by variations of the differentiation and proliferation rates between replicates of the experiment. Alternatively, we test a model with varying initial condition. CONCLUSIONS: We conclude by relating experimental variability to precise and identifiable variations between the replicates of the experiment of some model parameters. |
format | Online Article Text |
id | pubmed-8489053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84890532021-10-04 Practical identifiability in the frame of nonlinear mixed effects models: the example of the in vitro erythropoiesis Duchesne, Ronan Guillemin, Anissa Gandrillon, Olivier Crauste, Fabien BMC Bioinformatics Research BACKGROUND: Nonlinear mixed effects models provide a way to mathematically describe experimental data involving a lot of inter-individual heterogeneity. In order to assess their practical identifiability and estimate confidence intervals for their parameters, most mixed effects modelling programs use the Fisher Information Matrix. However, in complex nonlinear models, this approach can mask practical unidentifiabilities. RESULTS: Herein we rather propose a multistart approach, and use it to simplify our model by reducing the number of its parameters, in order to make it identifiable. Our model describes several cell populations involved in the in vitro differentiation of chicken erythroid progenitors grown in the same environment. Inter-individual variability observed in cell population counts is explained by variations of the differentiation and proliferation rates between replicates of the experiment. Alternatively, we test a model with varying initial condition. CONCLUSIONS: We conclude by relating experimental variability to precise and identifiable variations between the replicates of the experiment of some model parameters. BioMed Central 2021-10-04 /pmc/articles/PMC8489053/ /pubmed/34607573 http://dx.doi.org/10.1186/s12859-021-04373-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Duchesne, Ronan Guillemin, Anissa Gandrillon, Olivier Crauste, Fabien Practical identifiability in the frame of nonlinear mixed effects models: the example of the in vitro erythropoiesis |
title | Practical identifiability in the frame of nonlinear mixed effects models: the example of the in vitro erythropoiesis |
title_full | Practical identifiability in the frame of nonlinear mixed effects models: the example of the in vitro erythropoiesis |
title_fullStr | Practical identifiability in the frame of nonlinear mixed effects models: the example of the in vitro erythropoiesis |
title_full_unstemmed | Practical identifiability in the frame of nonlinear mixed effects models: the example of the in vitro erythropoiesis |
title_short | Practical identifiability in the frame of nonlinear mixed effects models: the example of the in vitro erythropoiesis |
title_sort | practical identifiability in the frame of nonlinear mixed effects models: the example of the in vitro erythropoiesis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489053/ https://www.ncbi.nlm.nih.gov/pubmed/34607573 http://dx.doi.org/10.1186/s12859-021-04373-4 |
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