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A Probabilistic Model for Cell Population Phenotyping Using HCS Data

High Content Screening (HCS) platforms allow screening living cells under a wide range of experimental conditions and give access to a whole panel of cellular responses to a specific treatment. The outcome is a series of cell population images. Within these images, the heterogeneity of cellular resp...

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Autores principales: Pauwels, Edouard, Surdez, Didier, Stoll, Gautier, Lescure, Aurianne, Del Nery, Elaine, Delattre, Olivier, Stoven, Véronique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3426525/
https://www.ncbi.nlm.nih.gov/pubmed/22927936
http://dx.doi.org/10.1371/journal.pone.0042715
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author Pauwels, Edouard
Surdez, Didier
Stoll, Gautier
Lescure, Aurianne
Del Nery, Elaine
Delattre, Olivier
Stoven, Véronique
author_facet Pauwels, Edouard
Surdez, Didier
Stoll, Gautier
Lescure, Aurianne
Del Nery, Elaine
Delattre, Olivier
Stoven, Véronique
author_sort Pauwels, Edouard
collection PubMed
description High Content Screening (HCS) platforms allow screening living cells under a wide range of experimental conditions and give access to a whole panel of cellular responses to a specific treatment. The outcome is a series of cell population images. Within these images, the heterogeneity of cellular response to the same treatment leads to a whole range of observed values for the recorded cellular features. Consequently, it is difficult to compare and interpret experiments. Moreover, the definition of phenotypic classes at a cell population level remains an open question, although this would ease experiments analyses. In the present work, we tackle these two questions. The input of the method is a series of cell population images for which segmentation and cellular phenotype classification has already been performed. We propose a probabilistic model to represent and later compare cell populations. The model is able to fully exploit the HCS-specific information: “dependence structure of population descriptors” and “within-population variability”. The experiments we carried out illustrate how our model accounts for this specific information, as well as the fact that the model benefits from considering them. We underline that these features allow richer HCS data analysis than simpler methods based on single cellular feature values averaged over each well. We validate an HCS data analysis method based on control experiments. It accounts for HCS specificities that were not taken into account by previous methods but have a sound biological meaning. Biological validation of previously unknown outputs of the method constitutes a future line of work.
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spelling pubmed-34265252012-08-27 A Probabilistic Model for Cell Population Phenotyping Using HCS Data Pauwels, Edouard Surdez, Didier Stoll, Gautier Lescure, Aurianne Del Nery, Elaine Delattre, Olivier Stoven, Véronique PLoS One Research Article High Content Screening (HCS) platforms allow screening living cells under a wide range of experimental conditions and give access to a whole panel of cellular responses to a specific treatment. The outcome is a series of cell population images. Within these images, the heterogeneity of cellular response to the same treatment leads to a whole range of observed values for the recorded cellular features. Consequently, it is difficult to compare and interpret experiments. Moreover, the definition of phenotypic classes at a cell population level remains an open question, although this would ease experiments analyses. In the present work, we tackle these two questions. The input of the method is a series of cell population images for which segmentation and cellular phenotype classification has already been performed. We propose a probabilistic model to represent and later compare cell populations. The model is able to fully exploit the HCS-specific information: “dependence structure of population descriptors” and “within-population variability”. The experiments we carried out illustrate how our model accounts for this specific information, as well as the fact that the model benefits from considering them. We underline that these features allow richer HCS data analysis than simpler methods based on single cellular feature values averaged over each well. We validate an HCS data analysis method based on control experiments. It accounts for HCS specificities that were not taken into account by previous methods but have a sound biological meaning. Biological validation of previously unknown outputs of the method constitutes a future line of work. Public Library of Science 2012-08-23 /pmc/articles/PMC3426525/ /pubmed/22927936 http://dx.doi.org/10.1371/journal.pone.0042715 Text en © 2012 Pauwels et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pauwels, Edouard
Surdez, Didier
Stoll, Gautier
Lescure, Aurianne
Del Nery, Elaine
Delattre, Olivier
Stoven, Véronique
A Probabilistic Model for Cell Population Phenotyping Using HCS Data
title A Probabilistic Model for Cell Population Phenotyping Using HCS Data
title_full A Probabilistic Model for Cell Population Phenotyping Using HCS Data
title_fullStr A Probabilistic Model for Cell Population Phenotyping Using HCS Data
title_full_unstemmed A Probabilistic Model for Cell Population Phenotyping Using HCS Data
title_short A Probabilistic Model for Cell Population Phenotyping Using HCS Data
title_sort probabilistic model for cell population phenotyping using hcs data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3426525/
https://www.ncbi.nlm.nih.gov/pubmed/22927936
http://dx.doi.org/10.1371/journal.pone.0042715
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