Relative transcript quantification by quantitative PCR: roughly right or precisely wrong?

BMC Mol Biol. 2005 Apr 26:6:10. doi: 10.1186/1471-2199-6-10.

Abstract

Background: When estimating relative transcript abundances by quantitative real-time PCR (Q-PCR) we found that the results can vary dramatically depending on the method chosen for data analysis.

Results: Analyses of Q-PCR results from a salmon louse starvation experiment show that, even with apparently good raw data, different analytical approaches 12 may lead to opposing biological conclusions.

Conclusion: The results emphasise the importance of being cautious when analysing Q-PCR data and indicate that uncritical routine application of an analytical method will eventually result in incorrect conclusions. We do not know the extent of, or have a universal solution to this problem. However, we strongly recommend caution when analysing Q-PCR results e.g. by using two or more analytical approaches to validate conclusions. In our view a common effort should be made to standardise methods for analysis and validation of Q-PCR results.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Copepoda / chemistry
  • Gene Expression Profiling / methods*
  • Polymerase Chain Reaction / methods*
  • Reproducibility of Results
  • Research Design*
  • Reverse Transcription
  • Sensitivity and Specificity