Hi Anbarasu.

To extract just the raw probe intensities (before BG adjustment or 
normalization), how about something like:


cdf <- AffymetrixCdfFile$byChipType(chipType, tags="coreR3,A20071112,EP")
cs <- AffymetrixCelSet$byName("tissues", cdf=cdf)

u <- 1:nbrOfUnits(cdf)
u <- 1:10  # could use line above, but use subset to make it quick

ugcM <- getUnitGroupCellMap(cdf, units=u, retNames=TRUE)
d <- extractMatrix(cs, cells=ugcM$cell)
rownames(d) <- paste(ugcM$unit, ugcM$group, sep=".")

There are of course other possibilities for the rownames if you chose, but here 
is what it would give:

> rownames(d) <- paste(ugcM$unit, ugcM$group, sep=".")
> head(d)
                huex_wta_spleen_A huex_wta_spleen_B huex_wta_spleen_C
2315251.2315252                49                46                30
2315251.2315252                41                48                37
2315251.2315252                68                46                40
2315251.2315252                46                39                32
2315251.2315253                34                26                31
2315251.2315253                30                30                28
                huex_wta_testes_A huex_wta_testes_B huex_wta_testes_C
2315251.2315252               131               111               156
2315251.2315252                96                81               153
2315251.2315252               138               102               146
2315251.2315252                72                49                56
2315251.2315253                45                33                48
2315251.2315253                30                39                31
                huex_wta_thyroid_A huex_wta_thyroid_B huex_wta_thyroid_C
2315251.2315252                 31                 57                 70
2315251.2315252                 49                 40                 63
2315251.2315252                 33                 54                 61
2315251.2315252                 30                 53                 46
2315251.2315253                 29                 53                 35
2315251.2315253                 26                 38                 39


Hope that helps.
Mark

On 2011-02-09, at 3:38 AM, Anbarasu L A wrote:

> Hi All,
> 
> I have been looking at extracting raw data for core transcripts from 
> HuEx-1_0-st-v2 chip type. I have downloaded the custom CDF file provided in 
> http://www.aroma-project.org/node/122. 
> 
> chipType <- "HuEx-1_0-st-v2"
> cdf <- AffymetrixCdfFile$byChipType(chipType, tags="core")
> print(cdf)
> AffymetrixCdfFile:
> Path: annotationData/chipTypes/HuEx-1_0-st-v2
> Filename: HuEx-1_0-st-v2,core.cdf
> Filesize: 32.00MB
> Chip type: HuEx-1_0-st-v2,core
> RAM: 0.00MB
> File format: v4 (binary; XDA)
> Dimension: 2560x2560
> Number of cells: 6553600
> Number of units: 22010
> Cells per unit: 297.76
> Number of QC units: 0
> 
> How can I access these 22010 units (transcripts) and extract un normalized 
> intensity values? If I use: getCellIndices(cdf, unlist=TRUE, useNames=FALSE), 
> I am getting intensity data for 893395 probes. 
> 
> Thanks in advance.
> 
> Best regards,
> Anbarasu 
> 
> 
> 
> 
> 
> -- 
> When reporting problems on aroma.affymetrix, make sure 1) to run the latest 
> version of the package, 2) to report the output of sessionInfo() and 
> traceback(), and 3) to post a complete code example.
>  
>  
> You received this message because you are subscribed to the Google Groups 
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> To post to this group, send email to aroma-affymetrix@googlegroups.com
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------------------------------
Mark Robinson, PhD (Melb)
Epigenetics Laboratory, Garvan
Bioinformatics Division, WEHI
e: mrobin...@wehi.edu.au
e: m.robin...@garvan.org.au
p: +61 (0)3 9345 2628
f: +61 (0)3 9347 0852
------------------------------


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version of the package, 2) to report the output of sessionInfo() and 
traceback(), and 3) to post a complete code example.


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