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A novel data fusion method for the effective analysis of multiple panels of flow cytometry data

Multicolour flow cytometry (MFC) is used to measure multiple cellular markers at the single-cell level. Cellular markers may be coloured with different panels of fluorescently-labelled antibodies to enable cell identification or the detection of activated cells in pre-defined, ‘gated’ specific cell...

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Autores principales: Tinnevelt, Gerjen H., van Staveren, Selma, Wouters, Kristiaan, Wijnands, Erwin, Verboven, Kenneth, Folcarelli, Rita, Koenderman, Leo, Buydens, Lutgarde M. C., Jansen, Jeroen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494873/
https://www.ncbi.nlm.nih.gov/pubmed/31043667
http://dx.doi.org/10.1038/s41598-019-43166-x
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author Tinnevelt, Gerjen H.
van Staveren, Selma
Wouters, Kristiaan
Wijnands, Erwin
Verboven, Kenneth
Folcarelli, Rita
Koenderman, Leo
Buydens, Lutgarde M. C.
Jansen, Jeroen J.
author_facet Tinnevelt, Gerjen H.
van Staveren, Selma
Wouters, Kristiaan
Wijnands, Erwin
Verboven, Kenneth
Folcarelli, Rita
Koenderman, Leo
Buydens, Lutgarde M. C.
Jansen, Jeroen J.
author_sort Tinnevelt, Gerjen H.
collection PubMed
description Multicolour flow cytometry (MFC) is used to measure multiple cellular markers at the single-cell level. Cellular markers may be coloured with different panels of fluorescently-labelled antibodies to enable cell identification or the detection of activated cells in pre-defined, ‘gated’ specific cell subsets. The number of markers that can be used per measurement is technologically limited however, requiring every panel to be analysed in a separate aliquot measurement. The combined analyses of these dedicated panels may enhance the predictive ability of these measurements and could enrich the interpretation of the immunological information. Here we introduce a fusion method for MFC data, based on DAMACY (Discriminant Analysis of Multi-Aspect Cytometry data), which can combine information from complementary panels. This approach leads to both enhanced predictions and clearer interpretations in comparison with the analysis of separate measurements. We illustrate this method using two datasets: the response of neutrophils evoked by a systemic endotoxin challenge and the activated immune status of the innate cells, T cells and B cells in obese versus lean individuals. The data fusion approach was able to detect cells that do not individually show a difference between clinical phenotypes but do play a role in combination with other cells.
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spelling pubmed-64948732019-05-17 A novel data fusion method for the effective analysis of multiple panels of flow cytometry data Tinnevelt, Gerjen H. van Staveren, Selma Wouters, Kristiaan Wijnands, Erwin Verboven, Kenneth Folcarelli, Rita Koenderman, Leo Buydens, Lutgarde M. C. Jansen, Jeroen J. Sci Rep Article Multicolour flow cytometry (MFC) is used to measure multiple cellular markers at the single-cell level. Cellular markers may be coloured with different panels of fluorescently-labelled antibodies to enable cell identification or the detection of activated cells in pre-defined, ‘gated’ specific cell subsets. The number of markers that can be used per measurement is technologically limited however, requiring every panel to be analysed in a separate aliquot measurement. The combined analyses of these dedicated panels may enhance the predictive ability of these measurements and could enrich the interpretation of the immunological information. Here we introduce a fusion method for MFC data, based on DAMACY (Discriminant Analysis of Multi-Aspect Cytometry data), which can combine information from complementary panels. This approach leads to both enhanced predictions and clearer interpretations in comparison with the analysis of separate measurements. We illustrate this method using two datasets: the response of neutrophils evoked by a systemic endotoxin challenge and the activated immune status of the innate cells, T cells and B cells in obese versus lean individuals. The data fusion approach was able to detect cells that do not individually show a difference between clinical phenotypes but do play a role in combination with other cells. Nature Publishing Group UK 2019-05-01 /pmc/articles/PMC6494873/ /pubmed/31043667 http://dx.doi.org/10.1038/s41598-019-43166-x Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tinnevelt, Gerjen H.
van Staveren, Selma
Wouters, Kristiaan
Wijnands, Erwin
Verboven, Kenneth
Folcarelli, Rita
Koenderman, Leo
Buydens, Lutgarde M. C.
Jansen, Jeroen J.
A novel data fusion method for the effective analysis of multiple panels of flow cytometry data
title A novel data fusion method for the effective analysis of multiple panels of flow cytometry data
title_full A novel data fusion method for the effective analysis of multiple panels of flow cytometry data
title_fullStr A novel data fusion method for the effective analysis of multiple panels of flow cytometry data
title_full_unstemmed A novel data fusion method for the effective analysis of multiple panels of flow cytometry data
title_short A novel data fusion method for the effective analysis of multiple panels of flow cytometry data
title_sort novel data fusion method for the effective analysis of multiple panels of flow cytometry data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494873/
https://www.ncbi.nlm.nih.gov/pubmed/31043667
http://dx.doi.org/10.1038/s41598-019-43166-x
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