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Updated: Apr 29, 2026

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA
Published on: January 22, 2018
Considerations for accurate gene expression measurement by reverse transcription quantitative PCR when analysing
Rebecca Sanders1, Deborah J Mason, Carole A Foy
1Molecular & Cell Biology, LGC, Queens Road, Teddington, TW11 0LY, UK, rebecca.sanders@lgcgroup.com.
Abstract:
Reverse transcription quantitative PCR is an established, simple and effective method for RNA measurement. However, technical standardisation challenges combined with frequent insufficient experimental detail render replication of many published findings challenging. Consequently, without adequate consideration of experimental standardisation, such findings may be sufficient for a given publication but cannot be translated to wider clinical application. This article builds on earlier standardisation work and the MIQE guidelines, discussing processes that need consideration for accurate, reproducible analysis when dealing with patient samples. By applying considerations common to the science of measurement (metrology), one can maximise the impact of gene expression studies, increasing the likelihood of their translation to clinical tools.

