Standardized determination of real-time PCR efficiency from a single reaction set-up

Nucleic Acids Res. 2003 Oct 15;31(20):e122. doi: 10.1093/nar/gng122.

Abstract

We propose a computing method for the estimation of real-time PCR amplification efficiency. It is based on a statistic delimitation of the beginning of exponentially behaving observations in real-time PCR kinetics. PCR ground fluorescence phase, non-exponential and plateau phase were excluded from the calculation process by separate mathematical algorithms. We validated the method on experimental data on multiple targets obtained on the LightCycler platform. The developed method yields results of higher accuracy than the currently used method of serial dilutions for amplification efficiency estimation. The single reaction set-up estimation is sensitive to differences in starting concentrations of the target sequence in samples. Furthermore, it resists the subjective influence of researchers, and the estimation can therefore be fully instrumentalized.

MeSH terms

  • Algorithms
  • Animals
  • Benzothiazoles
  • Cattle
  • DNA / chemistry
  • DNA / genetics
  • Diamines
  • Fluorescence
  • Genes, sry / genetics
  • Organic Chemicals / chemistry
  • Plasmids / genetics
  • Polymerase Chain Reaction / instrumentation
  • Polymerase Chain Reaction / methods*
  • Polymerase Chain Reaction / standards*
  • Quinolines
  • Reference Standards
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Benzothiazoles
  • Diamines
  • Organic Chemicals
  • Quinolines
  • SYBR Green I
  • DNA