Using a custom CDF file
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Nathan Haigh ▴ 120
@nathan-haigh-2307
Last seen 9.6 years ago
I'm using the xspecies [1] approach of hybridising gDNA to the Affy ATH1 chip. Using these, one masks out low intensity probes and creates a new CDF file - this is done several times using a different intensity threshold. I then want to analyse RNA hybs to the ATH1 chip using each of these different CDF files. Is it possible, for example, to tell ReadAffy() to use a certain CDF file? If so, I could write a nice R script to do all the processing etc. Or do I have to make a CDF package? If so, how/when do I specify the CDF file to use? I'm new to R/Bioconductor, so would appreciate any help towards this. Cheers Nathan [1] http://affymetrix.arabidopsis.info/xspecies/
cdf cdf • 1.5k views
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@james-w-macdonald-5106
Last seen 2 hours ago
United States
Hi Nathan, Nathan Haigh wrote: > I'm using the xspecies [1] approach of hybridising gDNA to the Affy ATH1 > chip. Using these, one masks out low intensity probes and creates a new > CDF file - this is done several times using a different intensity > threshold. I then want to analyse RNA hybs to the ATH1 chip using each > of these different CDF files. > > Is it possible, for example, to tell ReadAffy() to use a certain CDF > file? If so, I could write a nice R script to do all the processing etc. > Or do I have to make a CDF package? If so, how/when do I specify the CDF > file to use? ReadAffy() doesn't use a cdf file. Rather, it uses either a cdf package or a cdf environment, both of which are created using the makecdfenv package. It would be simple to either make a series of cdf packages or cdfenvs and then use ReadAffy() using the 'cdfname' argument to point to each of the different packages in turn. There are tradeoffs to using either approach. If you build the packages, you have to install which requires extra work on both Windows and MacOS. However, the packages are more persistent than the envs which only exist for the current working session unless you save() them somewhere and load() them prior to running an analysis. Best, Jim > > I'm new to R/Bioconductor, so would appreciate any help towards this. > > Cheers > Nathan > > [1] http://affymetrix.arabidopsis.info/xspecies/ > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor
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James W. MacDonald wrote: > Hi Nathan, > > Nathan Haigh wrote: >> I'm using the xspecies [1] approach of hybridising gDNA to the Affy ATH1 >> chip. Using these, one masks out low intensity probes and creates a new >> CDF file - this is done several times using a different intensity >> threshold. I then want to analyse RNA hybs to the ATH1 chip using each >> of these different CDF files. >> >> Is it possible, for example, to tell ReadAffy() to use a certain CDF >> file? If so, I could write a nice R script to do all the processing etc. >> Or do I have to make a CDF package? If so, how/when do I specify the CDF >> file to use? > > ReadAffy() doesn't use a cdf file. Rather, it uses either a cdf > package or a cdf environment, both of which are created using the > makecdfenv package. It would be simple to either make a series of cdf > packages or cdfenvs and then use ReadAffy() using the 'cdfname' > argument to point to each of the different packages in turn. > > There are tradeoffs to using either approach. If you build the > packages, you have to install which requires extra work on both > Windows and MacOS. However, the packages are more persistent than the > envs which only exist for the current working session unless you > save() them somewhere and load() them prior to running an analysis. > > Best, > > Jim > Thanks for the clear help - I think the envs will be most suitable for my purpose - I'll give it a go soon. Cheers Nathan
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