I have some mean amount of DNA from my ChIP assay (A), and some mean amount from the IgG (B).
Call fold enrichment C. C=A/B
I have standard deviations for both A and B. However, If I calculate the standard deviation for C according to basic propagation of error rules for sample quotients, my standard deviation becomes impossibly large.
I'm looking for a different way to calculate a standard deviation, standard error, relative error or confidence interval for fold enrichment (C). I've heard that jackknife resampling or bootstrapping a CI may be my best bet, but both of those methods seem silly given that I have only 3 technical replicates (n).
Many thanks for your help!