Re: [aroma.affymetrix] Re: Problem creating csU MAT normalization

2011-07-11 Thread Henrik Bengtsson
# Path: probeData/eman,MN,lm/Mm_PromPR_v02 >> # Platform: Affymetrix >> # Chip type: Mm_PromPR_v02 >> # Number of arrays: 24 >> # Names: 0hDNA_1_WAS-KXX-110419-24-681_1, 0hDNA_2_WAS- >> KXX-110419-24-681_2, 0hDNA_3_WAS-KXX-110419-24-681_3, ..., 6hK4_3_WAS- >>

Re: [aroma.affymetrix] Re: Accessing individual probe intensities

2011-07-11 Thread Henrik Bengtsson
Hi. On Sun, Jul 10, 2011 at 11:05 PM, Maria Rodrigo-Domingo wrote: > Hi Henrik, > > Thanks a lot for your reply. > > I am aware that probes/cells are not annotated just like probesets or > transcript clusters, so I just didn't explain my problem properly. I > have already done the analysis at the

Re: [aroma.affymetrix] exon level data.frame dimensions

2011-07-11 Thread Henrik Bengtsson
Hi. On Mon, Jul 11, 2011 at 5:33 AM, Anita wrote: > Dear group, > > I would like to extract a data.frame on the exon level and followed > these commands (see below), surprisingly the data.frame had these > dimensions: > > 326983 249 > > while I expected to have a data.frame with > 1.4 Mill 249 sa

[aroma.affymetrix] exon level data.frame dimensions

2011-07-11 Thread Anita
Dear group, I would like to extract a data.frame on the exon level and followed these commands (see below), surprisingly the data.frame had these dimensions: 326983 249 while I expected to have a data.frame with 1.4 Mill 249 samples Could you please advise me how I can extract the data for all

[aroma.affymetrix] Re: FIRMA: using setMergeGroups() for ExonRmaPlm to define groups

2011-07-11 Thread Marlen Mueller
Hello, Here is an update of my problem : Maybe I was not so clear with my general description: I have an exon tiling array as input (CDF) and did the first 2 steps of the RMA analysis using 6 CEL files which contains the raw intensities (3 flower replicates and 3 leaf replicates). I want to find