Re-annotation of probes for an Affy custom microarray
1
0
Entering edit mode
@ariel-grostern-4705
Last seen 9.6 years ago
Hello, I have a custom Affy Genechip that was designed using a draft version of a bacterial genome. We now have the finished version of the genome sequence available, so I would like to re-annotate the microarray probes to reflect the new genome sequence and gene numbering system. This problem appears to be something that many groups deal with on a regular basis, and I know that Affy constantly updates its annotation. Therefore, I was wondering if anyone could guide me in how I can go about re-annotating my array probes? Perhaps you have a pipeline that would be easily adapted to my probes and genome sequence? I know the basic sequence of events: map probes to new gene set->take list of exact matches->re-group probes->create CDF, but I don't know how to actually achieve these steps. Thank you for any help or points you can provide. Ariel Grostern post-doctoral researcher Alvarez-Cohen Lab Civil and Environmental Engineering UC Berkeley arielDOTgrosternATberkeleyDOTedu [[alternative HTML version deleted]]
Annotation cdf affy Annotation cdf affy • 1.1k views
ADD COMMENT
0
Entering edit mode
Laurent Gautier ★ 2.3k
@laurent-gautier-29
Last seen 9.6 years ago
Hi, The package altcdfenvs was written for such use-cases. Best, L. On 2011-06-21 01:19, Ariel Grostern wrote: > Hello, > > I have a custom Affy Genechip that was designed using a draft version of a bacterial genome. We now have the finished version of the genome sequence available, so I would like to re-annotate the microarray probes to reflect the new genome sequence and gene numbering system. > > This problem appears to be something that many groups deal with on a regular basis, and I know that Affy constantly updates its annotation. > > Therefore, I was wondering if anyone could guide me in how I can go about re-annotating my array probes? Perhaps you have a pipeline that would be easily adapted to my probes and genome sequence? I know the basic sequence of events: map probes to new gene set->take list of exact matches->re-group probes->create CDF, but I don't know how to actually achieve these steps. > > Thank you for any help or points you can provide. > > Ariel Grostern > > post-doctoral researcher > Alvarez-Cohen Lab > Civil and Environmental Engineering > UC Berkeley > arielDOTgrosternATberkeleyDOTedu > > [[alternative HTML version deleted]] > > _______________________________________________ > Bioconductor mailing list > Bioconductor at r-project.org > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor
ADD COMMENT

Login before adding your answer.

Traffic: 1130 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6