Stochastic processes defining sensitivity and variability of internally calibrated quantitative NASBA‐based viral load assays

For quantitative assessment of virus particles in patient plasma samples various assays are commercially available. Typical performance characteristics for such assays are sensitivity, precision and the range of linearity. In order to assess these properties it is common practice to divide the range...

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Veröffentlicht in:Nucleic acids research 2002-12, Vol.30 (24), p.e137-e137
Hauptverfasser: Weusten, Jos J. A. M., Wouters, Pieter A. W. M., van Zuijlen, Martien C. A., van de Wiel, Paul A.
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container_end_page e137
container_issue 24
container_start_page e137
container_title Nucleic acids research
container_volume 30
creator Weusten, Jos J. A. M.
Wouters, Pieter A. W. M.
van Zuijlen, Martien C. A.
van de Wiel, Paul A.
description For quantitative assessment of virus particles in patient plasma samples various assays are commercially available. Typical performance characteristics for such assays are sensitivity, precision and the range of linearity. In order to assess these properties it is common practice to divide the range of inputs into subranges in order to apply different statistical models to evaluate these properties separately. We developed a general statistical model for internally calibrated amplification based viral load assays that combines these statistical properties in one powerful analysis. Based on the model an unambiguous definition of the lower limit of the linear range can be given. The proposed method of analysis was illustrated by a successful application to data generated by the NucliSens EasyQ HIV‐1 assay.
doi_str_mv 10.1093/nar/gnf137
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subjects HIV-1 - genetics
Humans
Models, Statistical
NAR Methods Online
Reference Standards
RNA, Viral - blood
RNA, Viral - genetics
RNA, Viral - standards
Sensitivity and Specificity
Stochastic Processes
Viral Load - methods
Viral Load - standards
Viral Load - statistics & numerical data
title Stochastic processes defining sensitivity and variability of internally calibrated quantitative NASBA‐based viral load assays
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