Dear community,
I am a newbie in Affy analysis with Bioconcuctor and, while 3'UTR arrays analysis results quite straightforward (normalisation, DE, enrichment analysis...), I am struggling when analysing mouse transcriptome array (MTA) data. I have some questions I would really appreciate to be answered by the community:
- When I read the cel files, it tells me the annotation of the
HTAFeatureSet
(why is it called HTA when it should be MTA?) object ispd.mta.1.0
. However, there's no pd.mta.1.0ENTREZID function to fetch the Entrez Ids from the probeset names once I normalise the raw data. How could I get that function? - What's the difference between normalisation with
target="probeset"
andtarget="core"
? - When I use
featureFilter
function from gene filter package, it gives me null results. It seems it doesn't find any Entrez Id. How could I solve this?
I would just like to read the files, get the probesets for the exons only (ignoring splicing variants), then aggregate the probes by probesets (per gene) and then do DE analysis across 3 samples, but the oligo vignette from bioconductor is not enough to understand how to do it.
No, I didn't, but I need to use bioconductor (I can write code in python and R, so programming is not an issue)