Will ddPCR replace qPCR technology?
Amplification efficiency higher than 100% would mean that in each qPCR cycle, more than two copies of the target sequence have been generated.
Is this possible?
How to present the ratio data?
Which are the most probable reasons for a false positive result and how to address the issue?
Researchers often wonder which statistical tests they should use with their qPCR data. Most frequently these questions arise when analysing gene expression data.
The scandal has led to the human community in the EU benefiting from the better labeling of foods!
Concise overview over the current situation.