Hi,
Thanks for reading, I would like to ask you for your opinion. I would like perform a methylation analysis comparing two groups of samples with a determined number of probes/genes, not using all the probes available in the array (this gene list comes from a literature search). My questions are:
- Should probe selection be done before the contrast? Reduce the number of probes to a few hundreds/thousands before any comparison.
- Should probe selection be done after the contrast? Use all the probes and do a heatmap, for example, only with selected probes.
- What statistical consequences any of this selections would have?
- Does anybody know how to perform the probe selection in a workflow using minfi/limma, for example? I am asking this because the annotation of the probes is done after performing the contrasts.
Any help will be much appreciated. Thanks
IOM
Hi Andrew,
Thanks very much for your response. As you say, reducing the number is not appropriate and I would expect those genes to be differentially methylated using all probes if they truly were (without the reduction), is that correct? Thanks
IOM
That is correct, yes.
Cheers
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