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  Institute of Cell and Molecular Science
Flow Cytometry Core Facility equipment, images used with permission by BD
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Rare event analysis

 

For the identification of small populations of cells (<5%) it is important to ensure that sufficient events are recorded to provide precision. A simple calculation, r = (100/CV) 2 where r is the number of events meeting the required criterion, can be used to   determine that size of the database that will provide a given precision.

This calculation has been used to construct a table [PDF 44KB] which can be used as a guide in all cases of rare event analysis.

Publications.

KD Henseleit, AP Wheeler, G Warnes, KM Braun. Complementary Whole mount Visualization and Flow Cytometry Strategies. Progenitor Cells : Methods & Protocols. Methods in Molecular Biology Vol 916. Eds KA Mace, KM Braun. ISBN 978-1-61779-979-2, 2012.

MG Valorani, A Germani, WR Otto, L Harper, A Biddle, CP Khoo, WR Lin, MI Hawa, P Tropel, MP Patrizi, P Pozzilli, MR Alison. Hypoxia increases Sca-1/CD44 co-expression in murine mesenchymal stem cells and enhances their adipogenic differentiation potential. Cell Tissue Res, DOI 10.1007/s00441-010-0982-8 2010.

CP Khoo, MG Valorani, M Brittan, MR Alison, G Warnes, U Johansson, M Hawa, P Pozzilli. Characterization of endothelial progenitor cells in the NOD mouse as a source for cell therapies. Diabetes Metab Res Rev 25(1): 89-93, 2009.

 
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by Gary Warnes. © Queen Mary, University of London 2007
Institute of Cell and Molecular Science, The Blizard Building, Barts and The London School of Medicine and Dentistry, 4 Newark Street, London E1 2AT, UK Tel: +44 (0)20 7882 2483, Fax: +44 (0)20 7882 2200