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Automated in-silico detection of cell populations in flow cytometry readouts and its application to leukemia disease monitoring

BACKGROUND: Identification of minor cell populations, e.g. leukemic blasts within blood samples, has become increasingly important in therapeutic disease monitoring. Modern flow cytometers enable researchers to reliably measure six and more variables, describing cellular size, granularity and expres...

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Autores principales: Toedling, Joern, Rhein, Peter, Ratei, Richard, Karawajew, Leonid, Spang, Rainer
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1501051/
https://www.ncbi.nlm.nih.gov/pubmed/16753055
http://dx.doi.org/10.1186/1471-2105-7-282
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author Toedling, Joern
Rhein, Peter
Ratei, Richard
Karawajew, Leonid
Spang, Rainer
author_facet Toedling, Joern
Rhein, Peter
Ratei, Richard
Karawajew, Leonid
Spang, Rainer
author_sort Toedling, Joern
collection PubMed
description BACKGROUND: Identification of minor cell populations, e.g. leukemic blasts within blood samples, has become increasingly important in therapeutic disease monitoring. Modern flow cytometers enable researchers to reliably measure six and more variables, describing cellular size, granularity and expression of cell-surface and intracellular proteins, for thousands of cells per second. Currently, analysis of cytometry readouts relies on visual inspection and manual gating of one- or two-dimensional projections of the data. This procedure, however, is labor-intensive and misses potential characteristic patterns in higher dimensions. RESULTS: Leukemic samples from patients with acute lymphoblastic leukemia at initial diagnosis and during induction therapy have been investigated by 4-color flow cytometry. We have utilized multivariate classification techniques, Support Vector Machines (SVM), to automate leukemic cell detection in cytometry. Classifiers were built on conventionally diagnosed training data. We assessed the detection accuracy on independent test data and analyzed marker expression of incongruently classified cells. SVM classification can recover manually gated leukemic cells with 99.78% sensitivity and 98.87% specificity. CONCLUSION: Multivariate classification techniques allow for automating cell population detection in cytometry readouts for diagnostic purposes. They potentially reduce time, costs and arbitrariness associated with these procedures. Due to their multivariate classification rules, they also allow for the reliable detection of small cell populations.
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spelling pubmed-15010512006-07-14 Automated in-silico detection of cell populations in flow cytometry readouts and its application to leukemia disease monitoring Toedling, Joern Rhein, Peter Ratei, Richard Karawajew, Leonid Spang, Rainer BMC Bioinformatics Research Article BACKGROUND: Identification of minor cell populations, e.g. leukemic blasts within blood samples, has become increasingly important in therapeutic disease monitoring. Modern flow cytometers enable researchers to reliably measure six and more variables, describing cellular size, granularity and expression of cell-surface and intracellular proteins, for thousands of cells per second. Currently, analysis of cytometry readouts relies on visual inspection and manual gating of one- or two-dimensional projections of the data. This procedure, however, is labor-intensive and misses potential characteristic patterns in higher dimensions. RESULTS: Leukemic samples from patients with acute lymphoblastic leukemia at initial diagnosis and during induction therapy have been investigated by 4-color flow cytometry. We have utilized multivariate classification techniques, Support Vector Machines (SVM), to automate leukemic cell detection in cytometry. Classifiers were built on conventionally diagnosed training data. We assessed the detection accuracy on independent test data and analyzed marker expression of incongruently classified cells. SVM classification can recover manually gated leukemic cells with 99.78% sensitivity and 98.87% specificity. CONCLUSION: Multivariate classification techniques allow for automating cell population detection in cytometry readouts for diagnostic purposes. They potentially reduce time, costs and arbitrariness associated with these procedures. Due to their multivariate classification rules, they also allow for the reliable detection of small cell populations. BioMed Central 2006-06-05 /pmc/articles/PMC1501051/ /pubmed/16753055 http://dx.doi.org/10.1186/1471-2105-7-282 Text en Copyright © 2006 Toedling 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 Research Article
Toedling, Joern
Rhein, Peter
Ratei, Richard
Karawajew, Leonid
Spang, Rainer
Automated in-silico detection of cell populations in flow cytometry readouts and its application to leukemia disease monitoring
title Automated in-silico detection of cell populations in flow cytometry readouts and its application to leukemia disease monitoring
title_full Automated in-silico detection of cell populations in flow cytometry readouts and its application to leukemia disease monitoring
title_fullStr Automated in-silico detection of cell populations in flow cytometry readouts and its application to leukemia disease monitoring
title_full_unstemmed Automated in-silico detection of cell populations in flow cytometry readouts and its application to leukemia disease monitoring
title_short Automated in-silico detection of cell populations in flow cytometry readouts and its application to leukemia disease monitoring
title_sort automated in-silico detection of cell populations in flow cytometry readouts and its application to leukemia disease monitoring
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1501051/
https://www.ncbi.nlm.nih.gov/pubmed/16753055
http://dx.doi.org/10.1186/1471-2105-7-282
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