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Variance in multiplex suspension array assays: intraplex method improves reliability

BACKGROUND: Flow cytometry based suspended microarray assays are susceptible to many sources of variance; multi-well replication and inter-instrument reproducibility is uncertain. METHOD AND RESULTS: An "intraplex" method was developed in order to minimize differences in sample readings be...

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Detalles Bibliográficos
Autor principal: Hanley, Brian
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2000462/
https://www.ncbi.nlm.nih.gov/pubmed/17727693
http://dx.doi.org/10.1186/1742-4682-4-32
Descripción
Sumario:BACKGROUND: Flow cytometry based suspended microarray assays are susceptible to many sources of variance; multi-well replication and inter-instrument reproducibility is uncertain. METHOD AND RESULTS: An "intraplex" method was developed in order to minimize differences in sample readings between instruments. A full intraplex assay consists of a set m of microparticle set classifications assaying for the same analyte, with each of the m classifier sets having different sensitivity to analyte, and n classifier sets replicating each of the m levels of sensitivity, where m > 1 (generally m > 4 would be used). CONCLUSION: The intraplex method can compensate adequately for the sources of variance that have been identified in suspended microarray assays. It requires no changes to current equipment in use, and is a superior method of constructing precision assays. Additionally, Luminex(® )users may want to consider the evidence that shows that despite calibration to the same standard, two instruments may not give similar results for all concentrations of analytes.