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Lloyd, Bryony
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20
@lloyd-bryony-4067
Last seen 10.4 years ago
Hi,
I was hoping that someone might be able to suggest a way forward with
some siRNA array data I have been asked to analyse. There are 3 cell
lines, each hybridised using triplicate samples onto Agilent two
colour arrays:
CL, CL_knockdown and CL_scrambled.
Only one siRNA that has been used against the target.
I have analysed the data with Limma, using CL_scrambled as the ref in
the design matrix. Unfortunately there are a substantial number of
differentially expressed genes between the CL and CL_scrambled which
will potentially confound the experiment.
Is there a recommended way to minimise the effect of potential off
target effects, is this a possibility?
Possibly contrasting (CL_knockdown) - ( CL) ?
Remove the intersection of differentially expressed genes between CLvs
CL_scrambled and CL-knockdown vs CL_scrambled ?
I'd appreciate any advice that you can give.
Bryony
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