Integrating hgu133a and hgu133a2
1
0
Entering edit mode
Chintanu ▴ 310
@chintanu-2646
Last seen 9.6 years ago
Hi, I'm trying to combine hgu133a and hgu133a2 for a single downstream analysis. It is my first attempt, and have recently come across the idea of the mixture CDF environment. As I try to move on down this road considering that this is perhaps "the" option I have, eventually I could only sense that something is going not in the right direction (as follows). Any suggestions and advice would indeed be valuable. Thanks. Chintanu > sessionInfo() R version 2.7.0 (2008-04-22) i386-pc-mingw32 locale: attached base packages: [1] splines tools stats graphics grDevices utils datasets methods base other attached packages: [1] hgu133acdf_2.2.0 hgu133aprobe_2.2.0 hgu133a2probe_2.2.0 hgu133a2cdf_2.2.0 matchprobes_1.12.0 MergeMaid_2.12.0 MASS_7.2-41 [8] survival_2.34-1 affy_1.18.0 preprocessCore_1.2.0 affyio_1.8.0 Biobase_2.0.0 > cdfName(Data_A) # Data_A is ReadAffy () of a set of CEL files [1] "HG-U133A" > cdfName(Data_B) # Data_B is ReadAffy () of another set of CEL files [1] "HG-U133A_2" > comBatch <- combineAffyBatch(list(Data_A, Data_B), c("hgu133aprobe", "hgu133a2probe"), newcdf = "hgu133aa2") package:hgu133aprobe hgu133aprobe package:hgu133a2probe hgu133a2probe 241837 unique probes in common > Data_C=comBatch$dat > hgu133aa2cdf=comBatch$cdf > "@"(Data_C, "cdfName", "hgu133aa2cdf") [1] "hgu133aa2" > "@"(Data_C, "cdfName") [1] "hgu133aa2" > class (Data_C) # Same for Data_A and Data_B [1] "AffyBatch" attr(,"package") [1] "affy" > summary (Data_C) Length Class Mode 20 AffyBatch S4 > summary (Data_B) Length Class Mode 6 AffyBatch S4 > summary (Data_A) Length Class Mode 14 AffyBatch S4 > show (Data_A) AffyBatch object size of arrays=712x712 features (8 kb) cdf=HG-U133A (22283 affyids) number of samples=14 number of genes=22283 annotation=hgu133a notes= > show (Data_B) AffyBatch object size of arrays=732x732 features (8 kb) cdf=HG-U133A_2 (22277 affyids) number of samples=6 number of genes=22277 annotation=hgu133a2 notes= > show (Data_C) AffyBatch object size of arrays=0x0 features (8 kb) cdf=hgu133aa2 (??? affyids) number of samples=20 Error in getCdfInfo(object) : Could not obtain CDF environment, problems encountered: Specified environment does not contain hgu133aa2 Library - package hgu133aa2cdf not installed Data for package affy did not contain hgu133aa2cdf Bioconductor - hgu133aa2cdf not available In addition: Warning message: missing cdf environment! in show(AffyBatch) [[alternative HTML version deleted]]
hgu133a2 hgu133a cdf affy hgu133a2 hgu133a cdf affy • 1.0k views
ADD COMMENT
0
Entering edit mode
Chintanu ▴ 310
@chintanu-2646
Last seen 9.6 years ago
Hi All, I'm repeating my earlier post below, as it didn't bring any reply. If you have worked in the mixture CDF environment, I would appreciate if you could give me some direction, please. -------- I'm trying to combine hgu133a and hgu133a2 for a single downstream analysis. It is my first attempt, and have recently come across the idea of the mixture CDF environment. As I try to move on down this road considering that this is perhaps "the" option I have, eventually I could only sense that something is going not in the right direction (as follows). Any suggestions and advice would indeed be valuable. Thanks. Chintanu > sessionInfo() R version 2.7.0 (2008-04-22) i386-pc-mingw32 locale: attached base packages: [1] splines tools stats graphics grDevices utils datasets methods base other attached packages: [1] hgu133acdf_2.2.0 hgu133aprobe_2.2.0 hgu133a2probe_2.2.0 hgu133a2cdf_2.2.0 matchprobes_1.12.0 MergeMaid_2.12.0 MASS_7.2-41 [8] survival_2.34-1 affy_1.18.0 preprocessCore_1.2.0 affyio_1.8.0 Biobase_2.0.0 > cdfName(Data_A) # Data_A is ReadAffy () of a set of CEL files [1] "HG-U133A" > cdfName(Data_B) # Data_B is ReadAffy () of another set of CEL files [1] "HG-U133A_2" > comBatch <- combineAffyBatch(list(Data_A, Data_B), c("hgu133aprobe", "hgu133a2probe"), newcdf = "hgu133aa2") package:hgu133aprobe hgu133aprobe package:hgu133a2probe hgu133a2probe 241837 unique probes in common > Data_C=comBatch$dat > hgu133aa2cdf=comBatch$cdf > "@"(Data_C, "cdfName", "hgu133aa2cdf") [1] "hgu133aa2" > "@"(Data_C, "cdfName") [1] "hgu133aa2" > class (Data_C) # Same for Data_A and Data_B [1] "AffyBatch" attr(,"package") [1] "affy" > summary (Data_C) Length Class Mode 20 AffyBatch S4 > summary (Data_B) Length Class Mode 6 AffyBatch S4 > summary (Data_A) Length Class Mode 14 AffyBatch S4 > show (Data_A) AffyBatch object size of arrays=712x712 features (8 kb) cdf=HG-U133A (22283 affyids) number of samples=14 number of genes=22283 annotation=hgu133a notes= > show (Data_B) AffyBatch object size of arrays=732x732 features (8 kb) cdf=HG-U133A_2 (22277 affyids) number of samples=6 number of genes=22277 annotation=hgu133a2 notes= > show (Data_C) AffyBatch object size of arrays=0x0 features (8 kb) cdf=hgu133aa2 (??? affyids) number of samples=20 Error in getCdfInfo(object) : Could not obtain CDF environment, problems encountered: Specified environment does not contain hgu133aa2 Library - package hgu133aa2cdf not installed Data for package affy did not contain hgu133aa2cdf Bioconductor - hgu133aa2cdf not available In addition: Warning message: missing cdf environment! in show(AffyBatch) [[alternative HTML version deleted]]
ADD COMMENT
0
Entering edit mode
Hi Chintanu, Probably the reason it does not get a reply is because the issue has been discussed many times and searching the mailing list archive will allow you to read all of those discussions and decide what you want to do. My view is that you should not do it this way, but rather normalize similar things and then use appropriate statistical models to integrate the resulting data sets. But others have other opinions and there are many suggestions. Robert Chintanu wrote: > Hi All, > > I'm repeating my earlier post below, as it didn't bring any reply. > If you have worked in the mixture CDF environment, I would appreciate if you > could give me some direction, please. > > -------- > I'm trying to combine hgu133a and hgu133a2 for a single downstream analysis. > It is my first attempt, and have recently come across the idea of the > mixture CDF environment. As I try to move on down this road considering that > this is perhaps "the" option I have, eventually I could only sense that > something is going not in the right direction (as follows). > > Any suggestions and advice would indeed be valuable. > > Thanks. > > Chintanu > > > >> sessionInfo() > R version 2.7.0 (2008-04-22) > i386-pc-mingw32 > > locale: > > attached base packages: > [1] splines tools stats graphics grDevices utils datasets > methods base > > other attached packages: > [1] hgu133acdf_2.2.0 hgu133aprobe_2.2.0 hgu133a2probe_2.2.0 > hgu133a2cdf_2.2.0 matchprobes_1.12.0 MergeMaid_2.12.0 MASS_7.2-41 > [8] survival_2.34-1 affy_1.18.0 preprocessCore_1.2.0 > affyio_1.8.0 Biobase_2.0.0 > > >> cdfName(Data_A) # Data_A is ReadAffy () of a > set of CEL files > [1] "HG-U133A" > >> cdfName(Data_B) # Data_B is ReadAffy () of > another set of CEL files > [1] "HG-U133A_2" > > >> comBatch <- combineAffyBatch(list(Data_A, Data_B), c("hgu133aprobe", > "hgu133a2probe"), > newcdf = "hgu133aa2") > package:hgu133aprobe hgu133aprobe > package:hgu133a2probe hgu133a2probe > 241837 unique probes in common > >> Data_C=comBatch$dat >> hgu133aa2cdf=comBatch$cdf > >> "@"(Data_C, "cdfName", "hgu133aa2cdf") > [1] "hgu133aa2" >> "@"(Data_C, "cdfName") > [1] "hgu133aa2" > > >> class (Data_C) # Same for Data_A and Data_B > [1] "AffyBatch" > attr(,"package") > [1] "affy" > > > >> summary (Data_C) > Length Class Mode > 20 AffyBatch S4 > >> summary (Data_B) > Length Class Mode > 6 AffyBatch S4 > >> summary (Data_A) > Length Class Mode > 14 AffyBatch S4 > > >> show (Data_A) > AffyBatch object > size of arrays=712x712 features (8 kb) > cdf=HG-U133A (22283 affyids) > number of samples=14 > number of genes=22283 > annotation=hgu133a > notes= > >> show (Data_B) > AffyBatch object > size of arrays=732x732 features (8 kb) > cdf=HG-U133A_2 (22277 affyids) > number of samples=6 > number of genes=22277 > annotation=hgu133a2 > notes= > > >> show (Data_C) > AffyBatch object > size of arrays=0x0 features (8 kb) > cdf=hgu133aa2 (??? affyids) > number of samples=20 > Error in getCdfInfo(object) : > Could not obtain CDF environment, problems encountered: > Specified environment does not contain hgu133aa2 > Library - package hgu133aa2cdf not installed > Data for package affy did not contain hgu133aa2cdf > Bioconductor - hgu133aa2cdf not available > In addition: Warning message: > missing cdf environment! in show(AffyBatch) > > [[alternative HTML version deleted]] > > _______________________________________________ > 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 > -- Robert Gentleman, PhD Program in Computational Biology Division of Public Health Sciences Fred Hutchinson Cancer Research Center 1100 Fairview Ave. N, M2-B876 PO Box 19024 Seattle, Washington 98109-1024 206-667-7700 rgentlem at fhcrc.org
ADD REPLY

Login before adding your answer.

Traffic: 554 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