Standardisation of data from real-time quantitative PCR methods – evaluation of outliers and comparison of calibration curves
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Open Access
- 7 December 2005
- journal article
- Published by Springer Nature in BMC Biotechnology
- Vol. 5 (1) , 31
- https://doi.org/10.1186/1472-6750-5-31
Abstract
Background: As real-time quantitative PCR (RT-QPCR) is increasingly being relied upon for the enforcement of legislation and regulations dependent upon the trace detection of DNA, focus has increased on the quality issues related to the technique. Recent work has focused on the identification of factors that contribute towards significant measurement uncertainty in the real-time quantitative PCR technique, through investigation of the experimental design and operating procedure. However, measurement uncertainty contributions made during the data analysis procedure have not been studied in detail. This paper presents two additional approaches for standardising data analysis through the novel application of statistical methods to RT-QPCR, in order to minimise potential uncertainty in results. Results: Experimental data was generated in order to develop the two aspects of data handling and analysis that can contribute towards measurement uncertainty in results. This paper describes preliminary aspects in standardising data through the application of statistical techniques to the area of RT-QPCR. The first aspect concerns the statistical identification and subsequent handling of outlying values arising from RT-QPCR, and discusses the implementation of ISO guidelines in relation to acceptance or rejection of outlying values. The second aspect relates to the development of an objective statistical test for the comparison of calibration curves. Conclusion: The preliminary statistical tests for outlying values and comparisons between calibration curves can be applied using basic functions found in standard spreadsheet software. These two aspects emphasise that the comparability of results arising from RT-QPCR needs further refinement and development at the data-handling phase. The implementation of standardised approaches to data analysis should further help minimise variation due to subjective judgements. The aspects described in this paper will help contribute towards the development of a set of best practice guidelines regarding standardising handling and interpretation of data arising from RT-QPCR experiments.Keywords
This publication has 36 references indexed in Scilit:
- Accurate and Robust Quantification of Circulating Fetal and Total DNA in Maternal Plasma from 5 to 41 Weeks of GestationClinical Chemistry, 2005
- Cloned plasmid DNA fragments as calibrators for controlling GMOs: different real-time duplex quantitative PCR methodsAnalytical and Bioanalytical Chemistry, 2003
- Development of a novel quantitative real-time RT-PCR assay for the simultaneous detection of all serotypes of Foot-and-mouth disease virusArchiv für die gesamte Virusforschung, 2003
- Methodology for detecting trace amounts of microchimeric DNA from peripheral murine white blood cells by real-time PCRBiological Procedures Online, 2003
- Novel techniques for the efficient reduction of data generated by charge-coupled device detectorsReview of Scientific Instruments, 2000
- Quantification of insulin-like growth factor-1 (IGF-1) mRNA: Development and validation of an internally standardised competitive reverse transcription-polymerase chain reactionExperimental and Clinical Endocrinology & Diabetes, 1998
- Real time quantitative PCR.Genome Research, 1996
- ANCOVA for nonparallel slopes: the Johnson-Neyman techniqueInternational Journal of Bio-Medical Computing, 1994
- Procedures for Detecting Outlying Observations in SamplesTechnometrics, 1969
- On the Kolmogorov-Smirnov Test for Normality with Mean and Variance UnknownJournal of the American Statistical Association, 1967