Automated analysis of high-throughput flow cytometry data from hematopoietic stem cell experiments
Flow cytometry (FCM) is a technology that allows the rapid quantification of physical and chemical properties of up to millions of cells in a sample. It is a technology commonly used in drug discovery, health research, medical diagnosis and treatment, and vaccine development. Recent technological a...
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ndltd-UBC-oai-circle.library.ubc.ca-2429-219302018-01-05T17:24:09Z Automated analysis of high-throughput flow cytometry data from hematopoietic stem cell experiments Cortes, Sérgio Adrián Flow cytometry (FCM) is a technology that allows the rapid quantification of physical and chemical properties of up to millions of cells in a sample. It is a technology commonly used in drug discovery, health research, medical diagnosis and treatment, and vaccine development. Recent technological advancements in optics and reagents allow the quantification of up to 21 parameters per cell and advancements in robotics allow the use of FCM as a high-throughput technology. Lagging in the development of FCM technologies is the data analysis component. Conventional analysis of FCM data is labour intensive, subjective, hard to reproduce, error prone and not standardized. Indeed, the traditional analysis represents one of the main bottlenecks for the future adoption of recent technological advancements in biomedical research and the clinical environment. Here, an analysis framework developed for the automated analysis of FCM data derived from hematopoietic stem cell (HSC) transplant experiments using data generated in the Terry Fox Laboratory is presented. The data analysis pipeline developed aims to simplify approaches to analyze such data and generated automated tools for accurate analysis and quality control. The tool presented achieves equivalent results when compared to the traditional analysis, but avoids the traditional need for continuous user interaction. Incorporated into the analysis pipeline, is a model to predict the repopulation outcome from the HSC transplant experiments. Because HSC purification strategies are typically below 50%, more than half of the mice transplanted with a single cell will not be repopulated. The repopulation prediction model showed a performance of correctly identifying 81% of the mice that did not showed a positive engraftment, while keeping the incorrect misclassification of positive engraftments below 5%. Science, Faculty of Graduate 2010-03-16T14:04:32Z 2010-03-16T14:04:32Z 2009 2010-05 Text Thesis/Dissertation http://hdl.handle.net/2429/21930 eng Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ University of British Columbia |
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English |
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description |
Flow cytometry (FCM) is a technology that allows the rapid quantification of physical and chemical properties of up to millions of cells in a sample. It is a technology commonly used in drug discovery, health research, medical diagnosis and treatment, and vaccine development. Recent technological advancements in optics and reagents allow the quantification of up to 21 parameters per cell and advancements in robotics allow the use of FCM as a high-throughput technology. Lagging in the development of FCM technologies is the data analysis component. Conventional analysis of FCM data is labour intensive, subjective, hard to reproduce, error prone and not standardized. Indeed, the traditional analysis represents one of the main bottlenecks for the future adoption of recent technological advancements in biomedical research and the clinical environment.
Here, an analysis framework developed for the automated analysis of FCM data derived from hematopoietic stem cell (HSC) transplant experiments using data generated in the Terry Fox Laboratory is presented. The data analysis pipeline developed aims to simplify approaches to analyze such data and generated automated tools for accurate analysis and quality control. The tool presented achieves equivalent results when compared to the traditional analysis, but avoids the traditional need for continuous user interaction.
Incorporated into the analysis pipeline, is a model to predict the repopulation outcome from the HSC transplant experiments. Because HSC purification strategies are typically below 50%, more than half of the mice transplanted with a single cell will not be repopulated. The repopulation prediction model showed a performance of correctly identifying 81% of the mice that did not showed a positive engraftment, while keeping the incorrect misclassification of positive engraftments below 5%. === Science, Faculty of === Graduate |
author |
Cortes, Sérgio Adrián |
spellingShingle |
Cortes, Sérgio Adrián Automated analysis of high-throughput flow cytometry data from hematopoietic stem cell experiments |
author_facet |
Cortes, Sérgio Adrián |
author_sort |
Cortes, Sérgio Adrián |
title |
Automated analysis of high-throughput flow cytometry data from hematopoietic stem cell experiments |
title_short |
Automated analysis of high-throughput flow cytometry data from hematopoietic stem cell experiments |
title_full |
Automated analysis of high-throughput flow cytometry data from hematopoietic stem cell experiments |
title_fullStr |
Automated analysis of high-throughput flow cytometry data from hematopoietic stem cell experiments |
title_full_unstemmed |
Automated analysis of high-throughput flow cytometry data from hematopoietic stem cell experiments |
title_sort |
automated analysis of high-throughput flow cytometry data from hematopoietic stem cell experiments |
publisher |
University of British Columbia |
publishDate |
2010 |
url |
http://hdl.handle.net/2429/21930 |
work_keys_str_mv |
AT cortessergioadrian automatedanalysisofhighthroughputflowcytometrydatafromhematopoieticstemcellexperiments |
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1718582360948080640 |