Some probe sets on microarrays cross-hybridise (hybridise to several target genes). If all possible targets were included this could skew the analysis in the favour of the cross-hybridising targets, however if only one is selected (at random?) or if the probe sets are left out entirely you might miss something important.
Is there any general concensus on how to deal with this problem?
I had read about these recently actually, I think I will try them out. I hadn't noticed before that they supply both gene-centric and transcript-centric CDFs, that's nice.