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dc.contributor.authorHasenauer, Jande
dc.contributor.authorWaldherr, Steffende
dc.contributor.authorDoszczak, Malgorzatade
dc.contributor.authorRadde, Nicolede
dc.contributor.authorScheurich, Peterde
dc.contributor.authorAllgöwer, Frankde
dc.date.accessioned2014-09-24de
dc.date.accessioned2016-03-31T07:54:47Z-
dc.date.available2014-09-24de
dc.date.available2016-03-31T07:54:47Z-
dc.date.issued2011de
dc.identifier.other414813421de
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-95447de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/2353-
dc.identifier.urihttp://dx.doi.org/10.18419/opus-2336-
dc.description.abstractBackground: 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.en
dc.language.isoende
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.subject.classificationParameterschätzung , Zellpopulation , Heterogenitätde
dc.subject.ddc570de
dc.subject.otherparameter estimation , cell population , heterogeneityen
dc.titleIdentification of models of heterogeneous cell populations from population snapshot dataen
dc.typearticlede
dc.date.updated2014-09-24de
ubs.fakultaetFakultät Energie-, Verfahrens- und Biotechnikde
ubs.fakultaetFakultät Konstruktions-, Produktions- und Fahrzeugtechnikde
ubs.institutInstitut für Zellbiologie und Immunologiede
ubs.institutInstitut für Systemtheorie und Regelungstechnikde
ubs.opusid9544de
ubs.publikation.sourceBMC bioinformatics 12 (2011), Nr. 125. URL http://dx.doi.org./10.1186/1471-2105-12-125de
ubs.publikation.typZeitschriftenartikelde
Enthalten in den Sammlungen:04 Fakultät Energie-, Verfahrens- und Biotechnik

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