Relative expression software tool (REST(C)) for group-wise comparison and statistical analysis of relative expression results in real-time PCR
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Open Access
- 1 May 2002
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 30 (9), 36e-36
- https://doi.org/10.1093/nar/30.9.e36
Abstract
Real-time reverse transcription followed by polymerase chain reaction (RT-PCR) is the most suitable method for the detection and quantification of mRNA. It offers high sensitivity, good reproducibility and a wide quantification range. Today, relative expression is increasingly used, where the expression of a target gene is standardised by a non-regulated reference gene. Several mathematical algorithms have been developed to compute an expression ratio, based on real-time PCR efficiency and the crossing point deviation of an unknown sample versus a control. But all published equations and available models for the calculation of relative expression ratio allow only for the determination of a single transcription difference between one control and one sample. Therefore a new software tool was established, named REST (relative expression software tool), which compares two groups, with up to 16 data points in a sample and 16 in a control group, for reference and up to four target genes. The mathematical model used is based on the PCR efficiencies and the mean crossing point deviation between the sample and control group. Subsequently, the expression ratio results of the four investigated transcripts are tested for significance by a randomisation test. Herein, development and application of REST is explained and the usefulness of relative expression in real-time PCR using REST is discussed. The latest software version of REST and examples for the correct use can be downloaded at http://www.wzw.tum.de/gene-quantification/.Keywords
This publication has 19 references indexed in Scilit:
- A new mathematical model for relative quantification in real-time RT-PCRNucleic Acids Research, 2001
- The PCR plateau phase – towards an understanding of its limitationsBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 2000
- Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assaysJournal of Molecular Endocrinology, 2000
- Evaluation of RNA Isolation Methods and Reference Genes for RT-PCR Analyses of Rare Target RNAcclm, 2000
- Analysis of gene expression in single oocytes and embryos by real-time rapid cycle fluorescence monitored RT-PCR.Molecular Human Reproduction, 1999
- Housekeeping genes as internal standards: use and limitsJournal of Biotechnology, 1999
- Developments in Quantitative PCRcclm, 1998
- Quantification of inRNA by Polymerase Chain Reaction (PCR) Using an Internal Standard and a Nonradioactive Detection MethodPublished by Springer Nature ,1997
- Kinetic PCR Analysis: Real-time Monitoring of DNA Amplification ReactionsNature Biotechnology, 1993
- Nitric oxide stimulates auto-ADP-ribosylation of glyceraldehyde-3-phosphate dehydrogenase.Proceedings of the National Academy of Sciences, 1992