Absolute quantification of real-time PCR data with stage signal difference analysis
Chuanbo Liu, Jin Wang

TL;DR
This paper introduces a novel qPCR quantification method that monitors fluorescence changes at each thermal cycle stage to accurately determine nucleic acid amounts, avoiding traditional efficiency assumptions.
Contribution
It develops a new absolute quantification approach by directly calculating PCR efficiency changes from fluorescence signals during thermal cycles.
Findings
Efficiency change during PCR is complex and non-monotonic.
The new method accurately quantifies nucleic acids without efficiency modeling.
Classical threshold methods are supplemented by this more precise approach.
Abstract
Real-time PCR, or Real-time Quantitative PCR (qPCR) is an effective approach to quantify nucleic acid samples. Given the complicated reaction system along with thermal cycles, there has been long-term confusion on accurately calculating the initial nucleic acid amounts from the fluorescence signals. Although many improved algorithms had been proposed, the classical threshold method is still the primary choice in the routine application. In this study, we will first illustrate the origin of the linear relationship between the threshold value and logarithm of the initial nucleic acid amount by reconstructing the PCR reaction process with stochastic simulations. We then develop a new method for the absolute quantification of nucleic acid samples with qPCR. By monitoring the fluorescence signal changes in every stage of the thermal cycle, we are able to calculate a representation of the…
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Taxonomy
TopicsMolecular Biology Techniques and Applications · Gene expression and cancer classification · Biosensors and Analytical Detection
