Literature DB >> 19057902

A quantitative approach for polymerase chain reactions based on a hidden Markov model.

Nadia Lalam1.   

Abstract

Polymerase chain reaction (PCR) is a major DNA amplification technology from molecular biology. The quantitative analysis of PCR aims at determining the initial amount of the DNA molecules from the observation of typically several PCR amplifications curves. The mainstream observation scheme of the DNA amplification during PCR involves fluorescence intensity measurements. Under the classical assumption that the measured fluorescence intensity is proportional to the amount of present DNA molecules, and under the assumption that these measurements are corrupted by an additive Gaussian noise, we analyze a single amplification curve using a hidden Markov model (HMM). The unknown parameters of the HMM may be separated into two parts. On the one hand, the parameters from the amplification process are the initial number of the DNA molecules and the replication efficiency, which is the probability of one molecule to be duplicated. On the other hand, the parameters from the observational scheme are the scale parameter allowing to convert the fluorescence intensity into the number of DNA molecules and the mean and variance characterizing the Gaussian noise. We use the maximum likelihood estimation procedure to infer the unknown parameters of the model from the exponential phase of a single amplification curve, the main parameter of interest for quantitative PCR being the initial amount of the DNA molecules. An illustrative example is provided.

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Year:  2008        PMID: 19057902     DOI: 10.1007/s00285-008-0238-3

Source DB:  PubMed          Journal:  J Math Biol        ISSN: 0303-6812            Impact factor:   2.259


  30 in total

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4.  Sigmoidal curve-fitting redefines quantitative real-time PCR with the prospective of developing automated high-throughput applications.

Authors:  R G Rutledge
Journal:  Nucleic Acids Res       Date:  2004-12-15       Impact factor: 16.971

5.  Random variation and concentration effects in PCR.

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6.  Use of the recursion formula of the Gompertz function for the quantitation of PCR-amplified templates.

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8.  A computer program for the estimation of protein and nucleic acid sequence diversity in random point mutagenesis libraries.

Authors:  Michael J Volles; Peter T Lansbury
Journal:  Nucleic Acids Res       Date:  2005-06-29       Impact factor: 16.971

9.  Evaluation of absolute quantitation by nonlinear regression in probe-based real-time PCR.

Authors:  Rasmus Goll; Trine Olsen; Guanglin Cui; Jon Florholmen
Journal:  BMC Bioinformatics       Date:  2006-03-03       Impact factor: 3.169

10.  Model based analysis of real-time PCR data from DNA binding dye protocols.

Authors:  Mariano J Alvarez; Guillermo J Vila-Ortiz; Mariano C Salibe; Osvaldo L Podhajcer; Fernando J Pitossi
Journal:  BMC Bioinformatics       Date:  2007-03-09       Impact factor: 3.169

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  1 in total

1.  Modeling bias and variation in the stochastic processes of small RNA sequencing.

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Journal:  Nucleic Acids Res       Date:  2017-06-20       Impact factor: 16.971

  1 in total

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