 Methodology article
 Open Access
 Published:
Critique of the pairwise method for estimating qPCR amplification efficiency: beware of correlated data!
BMC Bioinformatics volume 21, Article number: 291 (2020)
Abstract
Background
A recently proposed method for estimating qPCR amplification efficiency E analyzes fluorescence intensity ratios from pairs of points deemed to lie in the exponential growth region on the amplification curves for all reactions in a dilution series. This method suffers from a serious problem: The resulting ratios are highly correlated, as they involve multiple use of the raw data, for example, yielding ~ 250 E estimates from ~ 25 intensity readings. The resulting statistics for such estimates are falsely optimistic in their assessment of the estimation precision.
Results
Monte Carlo simulations confirm that the correlated pairs method yields precision estimates that are better than actual by a factor of two or more. This result is further supported by estimating E by both pairwise and C_{q} calibration methods for the 16 replicate datasets from the critiqued work, and then comparing the ensemble statistics for these methods.
Conclusion
Contrary to assertions in the proposing work, the pairwise method does not yield E estimates a factor of 2 more precise than estimates from C_{q} calibration fitting (the standard curve method). On the other hand, the statistically correct direct fit of the data to the model behind the pairwise method can yield E estimates of comparable precision. Ways in which the approach might be improved are discussed briefly.
Background
The goal of quantitative polymerase chain reaction (qPCR) is the quantification of small amounts of a targeted genetic material, either relative to a chosen reference substance [1, 2] or absolute [3,4,5]. The standard approach for the latter is the use of a calibration series obtained by amplifying a set of solutions containing the targeted species at known concentrations designed to encompass that of the unknown. The resulting data — usually fluorescence signal as a function of amplification cycle — are then analyzed to obtain a characteristic cycle marker called C_{q} (quantification cycle), which can be defined in several ways, including threshold signal (either absolute or relative) and first and secondderivative maxima [6,7,8]. Under the assumption that C_{q} falls in the region of exponential growth,
— where y_{0} is the fluorescence signal for N_{0} target molecules in cycle x = 0, and E is the amplification efficiency (1 ≤ E ≤ 2) — a plot of C_{q} vs log (N_{0}) is linear, with slope = − 1/log(E). The location of C_{q} for the unknown on this line thus determines its N_{0}.
To achieve adequate precision in such calibration (or standard curve) procedures, it is generally recommended to record the known curves in replicate, typically triplicate. That generally means 12–18 reactions (and ideally a comparable number of reactions for the unknown, but this is seldom followed). As an alternative to this dataintensive procedure, many workers have sought what might be considered the “holy grail” of qPCR — the estimation of N_{0} from just the curve(s) for the unknown [8]. This requires reliable estimation of E, which must be based on analysis of just the early growth region, because E declines to ~ 1 as the signal plateaus in the largex limit. If trustworthy E estimates can be obtained, then only a single calibration result is needed to relate y_{0} to N_{0} for the unknown, or not even that if information relating fluorescence signal to amplicon size can be trusted [9]. However, for most methods used to estimate E for single reactions (SR), the results are likely to be lowbiased, since E has already declined by the time the signal has risen above background sufficiently to permit its estimation [10].
Recently Panina, et al. (PGDW) have proposed a method for estimating E that might be considered an intermediate to the traditional C_{q} calibration method and the SR methods [11]. In it, signal values deemed to lie in the early growth phase on all the amplification curves in a dilution series are analyzed simultaneously to yield a single estimate of E. This “global” procedure is illustrated in their Fig. 2, part (a) of which is reproduced here in Fig. 1. The dilution factor here is 2, so the 9 points to be analyzed can be fitted to the two parameters y_{0} and E using.
where y_{0} refers to the most concentrated solution (leftmost curve, j = 0), x_{ij} is the ith cycle on the jth curve, and the data are assumed to be backgroundfree (baselined). Rather than do this, PGDW analyzed pairs of values, which might be fitted to.
In this case there would now be \( \left(\begin{array}{c}9\\ {}2\end{array}\right) \) = 36 pairs. However, PGDW chose to take ratios to eliminate y_{0}, estimating E from
where y_{j} and y_{i} are the signals of the pair, having cycle numbers x = j and i, respectively, and D2 and D1 are the dilution factors (powers of 2). Because of the factor in the denominator, pairs having the same cycle number must be excluded, reducing the number of pairs in this case from 36 to 31.
There is a fundamental statistical problem with this pairwise approach: The 36 (31) data values are not independent, rather are correlated, since many of them involve the same members of the initial 9 points, which are reasonably assumed to be independent. The problem here might be recognized more easily through the following example: Suppose we just want the average of 9 values. Recognizing that the standard error (SE) (standard deviation in the mean in this case) is proportional to \( 1/\sqrt{n} \), why not just take each value 4 times and thereby reduce the SE by a factor of 2? This might seem silly, but the use of pairwise differences or ratios is just a more complex version of the same idea. In short, the full information in the data set is contained in the original 9 points, and there is no way of manufacturing more information through any scheme that generates more apparent observations. Since most of the statistical tests employed by PGDW assume independent data, they too are unreliable when applied to these pairwise estimates.
qPCR fluorescence data are expected to have roughly constant noise in the baseline and early growth regions [10], and PGDW found this for their data. Calling this random data error σ_{y}, fits to Eq. 2 can properly use unweighted nonlinear LS (NLS). For the differences in Eq. 3, the same would hold for independent data, but now with variance = 2σ_{y}^{2} from error propagation [12]. Calculations for the 36differences model give a predicted SE for E smaller than that for the direct 9point model by a factor of 1.9, close to the factor 2 for the averages analogy given above. Again, this is for independent difference values, so it represents the apparent precision gain, but will not hold for the correlated actual differences.
The E_{ij} estimates from Eq. 4 have varying precision, requiring weighting for the averages and normalized residuals for assessing outliers. Neglecting this can drastically affect both the residuals analysis and the normality tests, even apart from the correlation problems. To get the weights, we apply error propagation to a modified version of Eq. 4,
The weights w_{ij} for averaging the E_{ij} are proportional to \( {\sigma}_{E_{ij}}^{2} \), with σ_{Z} = σ_{E}/E. Recognizing that the E estimates are narrowly distributed, this gives approximately
which heavily favors ratios obtained for large cycle differences. The normalized residuals are obtained by dividing \( \left({E}_{ij}\overline{E}\right) \) by \( {\sigma}_{E_{ij}} \).
These statistical flaws do not necessarily mean that the method of PGDW is of no value, just that the resulting statistics cannot be trusted. One test that compares the methods on equal footing is their performance in ensemble statistics, which can be done here, thanks to the 16 replicate 6concentration datasets collected by PGDW. Such ensemblebased statistics remain valid, though limited in precision for just 16 replicates. However, if the pairwise method is to be employed, its proper (and much easier) implementation is through direct fitting to Eq. 2. In what follows, I use Monte Carlo simulations to confirm that this direct fitting approach is better than the pairwise method. I also find that the C_{q} calibration results in PGDW are not optimal, rather can be improved significantly through better methods of estimating C_{q} [7]. Further, pairwise E estimates tend to be lowbiased for the same reason as found in [10].
Results
Figure 2 shows results obtained by fitting the data in Fig. 1 to the model of Eq. 2. The residuals are systematic, leading to an estimate of 10.7 for the data error. This systematic error becomes even clearer if the cycles are all dropped by 1 unit, giving Chisq = 40.83 (s_{y} = 2.4) and E = 1.854(19) (where figures in parentheses are in terms of final digits, meaning 1.854 ± 0.019 here). Alternatively, 12 points fall in the growth zone 20–180 adopted by PGDW and give E = 1.747(27) and s_{y} = 6.7. These results show the sensitivity to the selection of the growth zone and are consistent with a main finding of ref. [10], that when growth has proceeded far enough above background to be analyzed, E is already declining significantly.
Monte Carlo simulations were done on a 9point model resembling the second mentioned above, having E = 1.85 and σ_{y} = 2.4. For each generated data set, random normal error of magnitude σ_{y} was added to the 9 exact intensity values of the model, and these randomized data were then fitted directly to Eq. 2. Next the 36 differences were calculated and analyzed with the model of Eq. 3. Histogrammed results for E are shown in Fig. 3, with fits of the counts to the normal distribution. The Chisq (χ^{2}) value is consistent with expectations for the ν = 27 statistical degrees of freedom in the case of the 9point model, but greatly exceeds ν (28) for the pairs, showing that the E estimates from the pairs analysis are not normally distributed [13]. The σ value for the 9point model agrees with predictions, while that for the pairs exceeds predictions for independent data by more than a factor of 2 and the 9point results by 13%. Results for the ratios approach of Eq. 4 used by PGDW are similar to those for differences (see Supplementary Information, SI). These findings show that the parametric SEs and setbyby set statistics from pairs analysis greatly overestimate precision, while the actual precision is nominally worse than for the simpler direct analysis.
All 16 6reaction replicate sets from PGDW were analyzed by all three of these approaches, using the 20–180 RFU growth window employed by PGDW. The results (Fig. 4) follow expectations from the results of the MC simulations. The numbers of points range from 22 to 25, resulting in 231–300 differences analyzed by Eq. 3 and 211–277 by Eq. 4. The large number of differences leads to the vastly optimistic error bars and the excessive Chisq values (cf ν = 15) for these methods. The postSEs from these weighted means can be converted to effective SDs for each replicate set by multiplying by \( \sqrt{16} \), giving 0.0180, 0.0204, and 0.0189. Unweighted averaging gives 0.0201, 0.0228, and 0.0215. Since sampling estimates of SDs have relative SD = (2ν)^{1/2}(18%), all of these SDs can be considered statistically consistent. They are also all about a factor of 2 larger than reported by PGDW.
Before addressing this difference, I consider the other method of assessing the AE: calibration (standard curve) fitting of C_{q} vs. log(N_{0}). Figure 5 shows such fits of all C_{q}s reported by PGDW and those estimated from their data using the methods of ref. [7]. All of the latter gave χ^{2} values smaller than those from PGDW, with lowest for Cy0. The SI describes the procedures from [7] in detail, including modifications that gave even better Cy0 values (χ^{2} = 1.27). These were used to generate 6point standard curves for each of the 16 replicate sets. The E estimates from these are displayed in Fig. 6, where they show a clear decline with increasing dataset number, information not evident from the results in Fig. 4. Although the slope is statistically significant, it must be an artifact of the experiments. Accordingly, simple averaging yields E = 1.8008(91) for PGDW and 1.7956(52) for my results; the singleset SDs are larger by the factor 4, giving 0.0363 and 0.0207. The latter value agrees with results given earlier for analysis with Eqs. 2–4.
I turn now to a closer examination of the pairwise results of PGDW. The numbers of ratios analyzed by my routine are close to the numbers reported in their Table S8, but not identical. For example, for the first 4 replicate sets, my analysis included 254, 254, 257, and 256 values, while they report 258, 258, 244, and 241. PGDW deleted ~ 15 values from each set, judging them to be outliers. However, as shown in Fig. 7, with proper weighting, these values are ipso facto insignificant. Thus, the values in the designated outlier zone have average weight two orders of magnitude smaller than the overall maximum weight. I have examined the distributions of weighted residuals by binning these and fitting the resulting histograms to the normal distribution. Viewed collectively, the 7 sets I have analyzed are not convincingly normal, which is not surprising, considering the correlated nature of the data. Still, they are not radically nonnormal, as the χ^{2} values of these fits are consistent with probabilities ranging from 1 to 50% (see Supplementary information).
Comparison of my E estimates with those in Table S7 from [11] shows general agreement, except for the additional values from my routine. Thus, the statistical properties of my estimates must be essentially the same as those of PGDW. With proper weighting, the estimates for each replicate set appear more precise than without. For example, weighted averaging for the A1–6 set gives E = 1.7838(48), while unweighted averaging gives 1.8070(106), where the errors are the SEs. These would be the correct quantities for predicting the precision of estimation for the method, if the data were independent; and they appear to be what PGDW obtained from their MC resampling method. However, as already noted, these SEs are falsely optimistic because of the correlated data problem.
Conclusion
A detailed examination of the pairwise method of estimating AE from Panina, et al. [11] shows that the appearance of improved precision for the method is a spurious result of the inherent correlation of the data. When implemented in a statistically correct way, by direct fitting of the fluorescence data to Eq. 2, the method can yield E estimates of precision comparable to that obtained by the standard curve approach. However, in the present tests, the latter revealed a trend toward smaller E with the increasing number of the replicate dataset, a trend not evident from the Eq. 2 analysis.
Comparing the average E from C_{q} calibration [1.7956(52)] with that from Eq. 2 in Fig. 4 [1.7761(45)], we see that the latter is about two combined SEs lower than the former, thus marginally biased. It is possible that the simple exponential growth assumption in Eq. 2 could be replaced by a more realistic growth model, like the logistic model [16, 17],
in which E declines naturally in the growth region from its value E_{0} in the baseline region. This might permit expansion of the range of fitted points with little bias.
The case against the pairwise method presented here has been made partly on its performance in comparisons of ensemble statistics. In fact it is not unusual for the latter to show somewhat larger dispersion than expected on the basis of statistics for the individual values. Thus, e.g., in Fig. 4 the Eq. 2 results, which come from a statistically correct treatment, still give a χ^{2} value of 39.4 in the weighted average, as compared with the expected ν = 15. Similarly, the χ^{2} values for the fits in Fig. 6 are both about 25. Excessively large χ^{2} values can come from inadequacies in the fit model or from sources of variability other than random noise in the data, as must be responsible for the unphysical decline in E with dataset in Fig. 6. In fact, Spiess and I made just this argument in suggesting that excess ensemble dispersion might stem from imprecision in the volumetric methods used to prepare samples [7].
Methods
The leastsquares (LS) and Monte Carlo (MC) calculations employed procedures similar to those described in several previous works on qPCR analysis [7, 10, 15, 18]. For the former, the KaleidaGraph program and FORTRAN codes were employed. FORTRAN codes were used for the MC simulations, with typically 4 × 10^{4} data sets in a run. C_{q} estimates were obtained from the data of PGDW using the LL7 model as described in [7]; although these data have been baselined, a sloping baseline was included in the fit model to compensate for possible systematic errors from this baselining [10].
It is instructive to note that some correlated data, like differences obtained from the fluorescence data shown in Fig. 1, can be analyzed by LS methods that take the correlation into account. Differences can be represented by a linear transformation of the original data, with the transformation matrix L having mostly zeroes, with one value of + 1 and one of − 1 in each row [19, 20]. If the original data are independent and of constant uncertainty, then the difference values must be weighted by a matrix W = (L L^{T})^{− 1}. In order to obtain this inverse matrix, the determinant of (L L^{T}) must be nonzero. When this procedure is tried in the present case, this determinant = 0 when the number of differences exceeds 8 — a clear “tilt” from the attempt to exceed the information content in the original data. However, the correlated procedure succeeds when any 8 differences that sample all 9 points are fitted to Eq. 3, while a single one of the 9 values is fitted to Eq. 2. And it yields results for the parameters and their SEs that are identical to those from the direct fit of all points to Eq. 2. (There is no correlation problem if no data point is used more than once in generating the pairs; but that would mean only 4 pairs for 9 points, hence reduced precision.)
Availability of data and materials
All data analyzed here are either available from already published sources or were generated in Monte Carlo simulations. All results are displayed in the paper and provided in numerical tables in the Supplementary Information.
Abbreviations
 qPCR:

Quantitative polymerase chain reaction
 y and y_{0} :

Fluorescence signal above baseline at cycle x and at cycle 0
 AE and E :

Amplification efficiency
 C _{ q } :

Quantification cycle
 N _{0} :

Initial number of target molecules in sample
 FDM and SDM:

Cycles where y reaches its maximal first and second derivatives, respectively
 Cy0:

Intersection of a straight line tangent to the curve at the FDM with the baselinecorrected xaxis
 C _{ r } :

Threshold defined as a fraction of plateau level y_{max}
 LS:

Least squares
 χ ^{2} :

Chisquare
 w _{ i } :

Statistical weight for ith data point
 σ^{2} and σ :

Variance and standard deviation
 “Chisq” in KaleidaGraph fit results:

χ^{2} when w_{i} = 1/σ_{i}^{2}), sum of squared residuals otherwise
 ν :

Statistical degrees of freedom, = # of data points  # of adjustable parameters
 SD:

Standard deviation
 SE:

Parameter standard error
 SI:

Supplementary Information
References
 1.
Pfaffl MW. A new mathematical model for relative quantification in realtime RTPCR. Nucleic Acids Res. 2001;29:e45.
 2.
Tellinghuisen J. Using nonlinear least squares to assess relative expression and its uncertainty in realtime qPCR studies. Anal Biochem. 2016;496:1–3.
 3.
Bustin SA. Absolute quantification of mRNA using realtime reverse transcription polymerase chain reaction assays. J Mol Endocrinol. 2000;25:169–93.
 4.
Rutledge RG, Cote C. Mathematics of quantitative kinetic PCR and the application of standard curves. Nucleic Acids Res. 2003;31:e93.
 5.
Larionov A, Krause A, Miller W. A standard curve based method for relative real time PCR data processing. BMC Bioinformatics. 2005;6:62.
 6.
Svec D, Tichopad A, Novosadova V, Pfaffl MW, Kubista M. How good is a PCR efficiency estimate: recommendations for precise and robust qPCR efficiency estimates. Biomol Detect Quantification. 2015;3:9–16.
 7.
Tellinghuisen J, Spiess AN. qPCR data analysis: better results through iconoclasm. Biomol Detect Quantification. 2019;17:100084.
 8.
Ruijter JM, Pfaffl MW, Zhao S, Spiess AN, Boggy G, Blom J, Rutledge RG, Sisti D, Lievens A, De Preter K, Derveaux S, Hellemans J, Vandesompele J. Evaluation of qPCR curve analysis methods for reliable biomarker discovery: bias, resolution, precision, and implications. Methods. 2013;59:32–46.
 9.
Rutledge RG. Sigmoidal curvefitting redefines quantitative realtime PCR with the prospective of developing automated highthroughput applications. Nucleic Acids Res. 2004;32:e178.
 10.
Tellinghuisen J, Spiess AN. Bias and imprecision in analysis of realtime quantitative polymerase chain reaction data. Anal Chem. 2015;87:8925–31.
 11.
Panina Y, Germond A, David BG, Watanabe TM. Pairwise efficiency: a new mathematical approach to qPCR data analysis increases the precision of the calibration curve assay. BMC Bioinformatics. 2019;20:295.
 12.
Tellinghuisen J. Statistical error propagation. J Phys Chem A. 2001;105:3917–21.
 13.
Tellinghuisen J. Understanding least squares through Monte Carlo calculations. J Chem Educ. 2005;82:157–66.
 14.
Tellinghuisen J. Leastsquares analysis of data with uncertainty in y and x: algorithms in Excel and KaleidaGraph. J Chem Educ. 2018;95:970–7.
 15.
Tellinghuisen J, Spiess AN. Comparing realtime quantitative polymerase chain reaction analysis methods for precision, linearity, and accuracy of estimating amplification efficiency. Anal Biochem. 2014;449:76–82.
 16.
Chervoneva I, Li YY, Iglewicz B, Waldman S, Hyslop T. Relative quantification based on logistic models for individual polymerase chain reactions. Stat Med. 2007;26:5596–611.
 17.
Rutledge R, Stewart D. A kineticbased sigmoidal model for the polymerase chain reaction and its application to highcapacity quantitative realtime PCR. BMC Biotechnol. 2008;8:47.
 18.
Tellinghuisen J, Spiess AN. Statistical uncertainty and its propagation in the analysis of quantitative polymerase chain reaction data: comparison of methods. Anal Biochem. 2014;464:94–102.
 19.
Tellinghuisen J. A study of statistical error in isothermal titration calorimetry. Anal Biochem. 2003;321:79–88.
 20.
Tellinghuisen J. Fitting correlated data: a critique of the Guggenheim method and other difference techniques. J Phys Chem A. 2003;107:8779–83.
Funding
This work was not supported by any external source of funds.
Author information
Affiliations
Contributions
This work was prepared by a single author. The author(s) read and approved the final manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
Not applicable. This work involved statistical data analysis only.
Consent for publication
Not applicable. This work involved statistical data analysis only.
Competing interests
I declare no competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Additional file 1: Figure S1.
Histogrammed results for E estimated using pairs ratio method of Eq. 4, with fits to the normal distribution. Table S1.C_{q} estimates for all 96 reactions from [11] using methods from [7]. Tables S2S4. Results obtained analyzing data from [11] using Eqs. 2–4. Figure S2. Variance analysis of Cy0calibrationbased E estimates and their SEs. Figure S3. Fitted normal distributions for histogrammed normalized residuals from weighted averages of pairwise ratio E estimates for two of 16 replicate datasets.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
About this article
Cite this article
Tellinghuisen, J. Critique of the pairwise method for estimating qPCR amplification efficiency: beware of correlated data!. BMC Bioinformatics 21, 291 (2020). https://doi.org/10.1186/s12859020036044
Received:
Accepted:
Published:
Keywords
 qPCR
 Amplification efficiency
 Data analysis
 Weighted least squares
 Statistical errors
 Calibration
 Correlated data