[BioC] Working with low abundance probesets !!
sharonanandhi at gmail.com
Thu Dec 1 14:50:12 CET 2005
I am working with the Affy data set for which the max fold change is
around 1.7. Most of the probesets have a fold change between 1.2 and
1.5. I have done the standard data analysis procedure reccommanded by
many people in Bioconductor (starting with RMA extraction, difference
between 2-groups, t-test, p-val & corrected p-val etc). After doing
this, I have got only 20 significant genes, which has no biological
significance with the experiment. Now, I am thinking of trying other
measures instead of difference between groups. What kinds of measures
I should try?
Is there any method addressing the issue of detecting low abundance
probesets in Bioconductor?
Thanks in Advance.
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