Standardization procedure for flow cytometry data harmonization in prospective multicenter studies.

Le Lann, Lucas;Jouve, Pierre-Emmanuel;Alarcón-Riquelme, Marta;Jamin, Christophe;Lauwerys, Bernard;et.al.
(2020) Scientific Reports — Vol. 10, n° 1, p. 11567 [1-8[ (2020)

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Authors
  • Le Lann, Lucas
    Author
  • Jouve, Pierre-Emmanuel
    Author
  • Alarcón-Riquelme, Martaorcid-logo
    Author
  • Jamin, Christopheorcid-logo
    Author
  • De Groof, AurélieUCLouvain
    Collaborator
  • Ducreux, JulieUCLouvain
    Collaborator
  • Lauwerys, BernardUCLouvain
    Collaborator
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Abstract
One of the most challenging objective for clinical cytometry in prospective multicenter immunomonitoring trials is to compare frequencies, absolute numbers of leukocyte populations and further the mean fluorescence intensities of cell markers, especially when the data are generated from different instruments. Here, we describe an innovative standardization workflow to compare all data to carry out any large-scale, prospective multicentric flow cytometry analysis whatever the duration, the number or type of instruments required for the realization of such projects.
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Citations

Le Lann, L., Jouve, P.-E., Alarcón-Riquelme, M., Jamin, C., & Pers, J.-O. (2020). Standardization procedure for flow cytometry data harmonization in prospective multicenter studies. Scientific Reports, 10(1), 11567 [1-8[. https://doi.org/10.1038/s41598-020-68468-3 (Original work published 2020)