Impact of smoothing on parameter estimation in quantitative DNA amplification experiments
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Impact of smoothing on parameter estimation in quantitative DNA amplification experiments. / Spiess, Andrej-Nikolai; Deutschmann, Claudia; Burdukiewicz, Michał; Himmelreich, Ralf; Klat, Katharina; Schierack, Peter; Rödiger, Stefan.
In: CLIN CHEM, Vol. 61, No. 2, 02.2015, p. 379-88.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Impact of smoothing on parameter estimation in quantitative DNA amplification experiments
AU - Spiess, Andrej-Nikolai
AU - Deutschmann, Claudia
AU - Burdukiewicz, Michał
AU - Himmelreich, Ralf
AU - Klat, Katharina
AU - Schierack, Peter
AU - Rödiger, Stefan
N1 - © 2014 American Association for Clinical Chemistry.
PY - 2015/2
Y1 - 2015/2
N2 - BACKGROUND: Quantification cycle (Cq) and amplification efficiency (AE) are parameters mathematically extracted from raw data to characterize quantitative PCR (qPCR) reactions and quantify the copy number in a sample. Little attention has been paid to the effects of preprocessing and the use of smoothing or filtering approaches to compensate for noisy data. Existing algorithms largely are taken for granted, and it is unclear which of the various methods is most informative. We investigated the effect of smoothing and filtering algorithms on amplification curve data.METHODS: We obtained published high-replicate qPCR data sets from standard block thermocyclers and other cycler platforms and statistically evaluated the impact of smoothing on Cq and AE.RESULTS: Our results indicate that selected smoothing algorithms affect estimates of Cq and AE considerably. The commonly used moving average filter performed worst in all qPCR scenarios. The Savitzky-Golay smoother, cubic splines, and Whittaker smoother resulted overall in the least bias in our setting and exhibited low sensitivity to differences in qPCR AE, whereas other smoothers, such as running mean, introduced an AE-dependent bias.CONCLUSIONS: The selection of a smoothing algorithm is an important step in developing data analysis pipelines for real-time PCR experiments. We offer guidelines for selection of an appropriate smoothing algorithm in diagnostic qPCR applications. The findings of our study were implemented in the R packages chipPCR and qpcR as a basis for the implementation of an analytical strategy.
AB - BACKGROUND: Quantification cycle (Cq) and amplification efficiency (AE) are parameters mathematically extracted from raw data to characterize quantitative PCR (qPCR) reactions and quantify the copy number in a sample. Little attention has been paid to the effects of preprocessing and the use of smoothing or filtering approaches to compensate for noisy data. Existing algorithms largely are taken for granted, and it is unclear which of the various methods is most informative. We investigated the effect of smoothing and filtering algorithms on amplification curve data.METHODS: We obtained published high-replicate qPCR data sets from standard block thermocyclers and other cycler platforms and statistically evaluated the impact of smoothing on Cq and AE.RESULTS: Our results indicate that selected smoothing algorithms affect estimates of Cq and AE considerably. The commonly used moving average filter performed worst in all qPCR scenarios. The Savitzky-Golay smoother, cubic splines, and Whittaker smoother resulted overall in the least bias in our setting and exhibited low sensitivity to differences in qPCR AE, whereas other smoothers, such as running mean, introduced an AE-dependent bias.CONCLUSIONS: The selection of a smoothing algorithm is an important step in developing data analysis pipelines for real-time PCR experiments. We offer guidelines for selection of an appropriate smoothing algorithm in diagnostic qPCR applications. The findings of our study were implemented in the R packages chipPCR and qpcR as a basis for the implementation of an analytical strategy.
KW - Algorithms
KW - DNA
KW - Monte Carlo Method
KW - Real-Time Polymerase Chain Reaction
KW - Regression Analysis
U2 - 10.1373/clinchem.2014.230656
DO - 10.1373/clinchem.2014.230656
M3 - SCORING: Journal article
C2 - 25477537
VL - 61
SP - 379
EP - 388
JO - CLIN CHEM
JF - CLIN CHEM
SN - 0009-9147
IS - 2
ER -