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Identification of models of heterogeneous cell populations from population snapshot data
BACKGROUND: Most of the modeling performed in the area of systems biology aims at achieving a quantitative description of the intracellular pathways within a "typical cell". However, in many biologically important situations even clonal cell populations can show a heterogeneous response. T...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114742/ https://www.ncbi.nlm.nih.gov/pubmed/21527025 http://dx.doi.org/10.1186/1471-2105-12-125 |
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author | Hasenauer, Jan Waldherr, Steffen Doszczak, Malgorzata Radde, Nicole Scheurich, Peter Allgöwer, Frank |
author_facet | Hasenauer, Jan Waldherr, Steffen Doszczak, Malgorzata Radde, Nicole Scheurich, Peter Allgöwer, Frank |
author_sort | Hasenauer, Jan |
collection | PubMed |
description | BACKGROUND: Most of the modeling performed in the area of systems biology aims at achieving a quantitative description of the intracellular pathways within a "typical cell". However, in many biologically important situations even clonal cell populations can show a heterogeneous response. These situations require study of cell-to-cell variability and the development of models for heterogeneous cell populations. RESULTS: In this paper we consider cell populations in which the dynamics of every single cell is captured by a parameter dependent differential equation. Differences among cells are modeled by differences in parameters which are subject to a probability density. A novel Bayesian approach is presented to infer this probability density from population snapshot data, such as flow cytometric analysis, which do not provide single cell time series data. The presented approach can deal with sparse and noisy measurement data. Furthermore, it is appealing from an application point of view as in contrast to other methods the uncertainty of the resulting parameter distribution can directly be assessed. CONCLUSIONS: The proposed method is evaluated using artificial experimental data from a model of the tumor necrosis factor signaling network. We demonstrate that the methods are computationally efficient and yield good estimation result even for sparse data sets. |
format | Online Article Text |
id | pubmed-3114742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31147422011-06-15 Identification of models of heterogeneous cell populations from population snapshot data Hasenauer, Jan Waldherr, Steffen Doszczak, Malgorzata Radde, Nicole Scheurich, Peter Allgöwer, Frank BMC Bioinformatics Methodology Article BACKGROUND: Most of the modeling performed in the area of systems biology aims at achieving a quantitative description of the intracellular pathways within a "typical cell". However, in many biologically important situations even clonal cell populations can show a heterogeneous response. These situations require study of cell-to-cell variability and the development of models for heterogeneous cell populations. RESULTS: In this paper we consider cell populations in which the dynamics of every single cell is captured by a parameter dependent differential equation. Differences among cells are modeled by differences in parameters which are subject to a probability density. A novel Bayesian approach is presented to infer this probability density from population snapshot data, such as flow cytometric analysis, which do not provide single cell time series data. The presented approach can deal with sparse and noisy measurement data. Furthermore, it is appealing from an application point of view as in contrast to other methods the uncertainty of the resulting parameter distribution can directly be assessed. CONCLUSIONS: The proposed method is evaluated using artificial experimental data from a model of the tumor necrosis factor signaling network. We demonstrate that the methods are computationally efficient and yield good estimation result even for sparse data sets. BioMed Central 2011-04-28 /pmc/articles/PMC3114742/ /pubmed/21527025 http://dx.doi.org/10.1186/1471-2105-12-125 Text en Copyright ©2011 Hasenauer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Hasenauer, Jan Waldherr, Steffen Doszczak, Malgorzata Radde, Nicole Scheurich, Peter Allgöwer, Frank Identification of models of heterogeneous cell populations from population snapshot data |
title | Identification of models of heterogeneous cell populations from population snapshot data |
title_full | Identification of models of heterogeneous cell populations from population snapshot data |
title_fullStr | Identification of models of heterogeneous cell populations from population snapshot data |
title_full_unstemmed | Identification of models of heterogeneous cell populations from population snapshot data |
title_short | Identification of models of heterogeneous cell populations from population snapshot data |
title_sort | identification of models of heterogeneous cell populations from population snapshot data |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114742/ https://www.ncbi.nlm.nih.gov/pubmed/21527025 http://dx.doi.org/10.1186/1471-2105-12-125 |
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