Literature DB >> 16972087

Quantitative real-time RT-PCR data analysis: current concepts and the novel "gene expression's CT difference" formula.

Jan H Schefe1, Kerstin E Lehmann, Ivo R Buschmann, Thomas Unger, Heiko Funke-Kaiser.   

Abstract

For quantification of gene-specific mRNA, quantitative real-time RT-PCR has become one of the most frequently used methods over the last few years. This article focuses on the issue of real-time PCR data analysis and its mathematical background, offering a general concept for efficient, fast and precise data analysis superior to the commonly used comparative CT (DeltaDeltaCT) and the standard curve method, as it considers individual amplification efficiencies for every PCR. This concept is based on a novel formula for the calculation of relative gene expression ratios, termed GED (Gene Expression's CT Difference) formula. Prerequisites for this formula, such as real-time PCR kinetics, the concept of PCR efficiency and its determination, are discussed. Additionally, this article offers some technical considerations and information on statistical analysis of real-time PCR data.

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Year:  2006        PMID: 16972087     DOI: 10.1007/s00109-006-0097-6

Source DB:  PubMed          Journal:  J Mol Med (Berl)        ISSN: 0946-2716            Impact factor:   4.599


  29 in total

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

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Journal:  Genome Biol       Date:  2002-06-18       Impact factor: 13.583

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  296 in total

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7.  Quantitative evaluation and selection of reference genes in a rat model of extended liver resection.

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8.  Controlled microenvironments to evaluate chemotactic properties of cultured Müller glia.

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9.  Analyzing the promoters of two CYP9A genes in the silkworm Bombyx mori by dual-luciferase reporter assay.

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10.  DAX-1A (NR0B1A) expression levels are extremely low compared to DAX-1 (NR0B1) in human steroidogenic tissues.

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