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Quality-Controlled Sputum Analysis by Flow Cytometry
Published on: August 9, 2021
Overview of clinical flow cytometry data analysis: recent advances and future challenges
Carlos E Pedreira1, Elaine S Costa, Quentin Lecrevisse
1COPPE - Engineering Graduate Program and Faculty of Medicine, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
Trends in Biotechnology
|June 11, 2013
Summary
Technological advances in flow cytometry (FC) generate complex data. This review covers new analysis and visualization tools for more objective interpretation of FC data in research and diagnostics.
Area of Science:
- Biomedical research
- Clinical diagnostics
- Data science
Background:
- Recent decades have seen major technological advancements in flow cytometry (FC) instrumentation and reagents.
- These advances enable simultaneous analysis of more parameters per cell at increased speeds.
- This leads to the generation of large, complex datasets with information on millions of cells and tens of parameters.
Purpose of the Study:
- To review current data analysis and visualization strategies for flow cytometry (FC) data.
- To highlight methods that improve the objectivity and robustness of FC data interpretation.
- To address the challenges posed by increasingly complex FC datasets.
Main Methods:
- Review of conventional and newly developed data analysis algorithms.
- Examination of visualization techniques for high-dimensional flow cytometry data.
- Synthesis of strategies for interpreting complex FC datasets.
Main Results:
- Identification of a growing need for advanced data analysis tools in FC.
- Overview of emerging algorithms and software for handling large-scale FC data.
- Discussion of strategies for objective and robust interpretation of FC results.
Conclusions:
- New data analysis and visualization tools are essential for managing complex flow cytometry data.
- These tools facilitate more objective and robust interpretation of FC data.
- The reviewed strategies are applicable to both biomedical research and clinical diagnostic settings.
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