A fixed-point algorithm for estimating amplification efficiency from a polymerase chain reaction dilution series

dc.contributor.authorJones, Michael Emlyn
dc.contributor.authorMayne, George C
dc.contributor.authorWang, Tingting
dc.contributor.authorWatson, David Ian
dc.contributor.authorHussey, Damian James
dc.descriptionThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en
dc.description.abstractBackground The polymerase chain reaction amplifies and quantifies small amounts of DNA. It is a cyclic process, during each cycle of which each strand of template DNA is copied with probability approaching one: the amount of DNA approximately doubles and this amount can be estimated fluorimetrically each cycle, producing a set of fluorescence values hereafter referred to as the amplification curve. Commonly the biological question of relevance is one of the ratio of DNA concentrations in two samples: a ratio that is deduced by comparing the two amplification curves, usually by way of a plot of fluorescence against cycle number. Central to this analysis is measuring the extent to which one amplification curve is shifted relative to the other, a measurement often accomplished by defining a threshold or quantification cycle, Cq, for each curve: the fractional cycle number at which fluorescence reaches some threshold or at which some other criterion (maximum slope, maximum rate of change of slope) is satisfied. We propose an alternative where position is measured relative to a reference curve; position equates to the cycle shift which maximizes the correlation between the reference and the observed fluorescence sequence. A key parameter of the reference curve is obtained by fixed-point convergence. Results We consider the analysis of dilution series constructed for the estimation of qPCR amplification efficiency. The estimate of amplification efficiency is based on the slope of the regression line when the Cq is plotted against the logarithm of dilution. We compare the approach to three commonly used methods for determining Cq; each is applied to publicly accessible calibration data sets, and to ten from our own laboratory. As in the established literature we judge their relative merits both from the standard deviation of the slope of the calibration curve, and from the variance in Cq for replicate fluorescence curves. Conclusions The approach does not require modification of experimental protocols, and can be applied retrospectively to existing data. We recommend that it be added to the methodological toolkit with which laboratories interpret their real-time PCR data. Keywords: qPCR; Fixed-point; Amplification efficiencyen
dc.identifier.citationJones, ME, Mayne, GC, Wang, T, Watson DI & Hussey, DJ.: A fixed-point algorithm for estimating amplification efficiency from a polymerase chain reaction dilution series. BMC Bioinformatics 2014 15:372.en
dc.publisherBioMed Centralen
dc.rights© 2014 Jones et al.; licensee BioMed Central Ltd.en
dc.rights.holderJones et al.; licensee BioMed Central Ltd.en
dc.titleA fixed-point algorithm for estimating amplification efficiency from a polymerase chain reaction dilution seriesen
local.contributor.authorOrcidLookupHussey, Damian James: https://orcid.org/0000-0002-6121-6740en_US
local.contributor.authorOrcidLookupWatson, David Ian: https://orcid.org/0000-0002-7683-2693en_US
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