[aroma.affymetrix] Re: SNPs affecting EXon splicing detection

2009-06-11 Thread sabrina
Hi, Mark: for the Unit_id, does it have to be Ensembl gene ID like ENSMUSG? Lots of genes do not have ensembl assignment from Affy annotation file. There are lots of missing annotaions, and I still have not found any good way to deal with it. Do you have any suggestions? Thanks Sabrina On

[aroma.affymetrix] Re: SNPs affecting EXon splicing detection

2009-06-11 Thread Mark Robinson
Hi Sabrina. The Unit_ID can be any transcript cluster identifier of your choice. The easiest may be to use the Affymetrix transcript cluster identifier itself ... available from: http://www.affymetrix.com/analysis/downloads/current_exon/MoEx-1_0-st-v1.mm9.probeset.csv.zip See the

[aroma.affymetrix] Re: SNPs affecting EXon splicing detection

2009-06-09 Thread sabrina
Thanks , Mark! Can you show me /walk me through how to get a new snp-free CDF ? I finally got the right version of snp and probe mapping so I am ready to try it out! Sabrina On Jun 6, 3:14 am, Mark Robinson mrobin...@wehi.edu.au wrote: Hi Sabrina. Comments below. On 06/06/2009, at 1:57 AM,

[aroma.affymetrix] Re: SNPs affecting EXon splicing detection

2009-06-09 Thread Mark Robinson
Hi Sabrina. How about you try and create a 'flat' file like the one described at: http://groups.google.com/group/aroma-affymetrix/web/creating-cdf-files-from-scratch Presumably, you will be comfortable with the Exon Array's 'probetab' file by now and possibly the Affymetrix annotation CSV

[aroma.affymetrix] Re: SNPs affecting EXon splicing detection

2009-06-06 Thread Mark Robinson
Hi Sabrina. Comments below. On 06/06/2009, at 1:57 AM, sabrina wrote: Hi, Mark: I finally found the SNP data set that is suitable for my case. As I understand, aroma used RMA to estimate gene level and exon level intensities. After I estimate gene level (transcript level), I can use

[aroma.affymetrix] Re: SNPs affecting EXon splicing detection

2009-04-30 Thread Mark Robinson
Hi Sabrina. I have not had to deal with this myself, but I do know that it exists and I can at least suggest a possible route to exclude affected exons. Presumably, there is a database (dbSNP?) that tells you the genome locations of each SNP for your strains. There is also a probe.tab