Perhaps something like this is what you want (note: different chip to
what you are using)?

df <- readDataFrame(getCdf(cs), verbose=-80)
[...snip...]
head(df)
 unit unitName   unitType unitDirection unitNbrOfAtoms group groupName
1    1  7892501 expression         sense              4     1
7892501
2    1  7892501 expression         sense              4     1
7892501
3    1  7892501 expression         sense              4     1
7892501
4    1  7892501 expression         sense              4     1
7892501
5    2  7892502 expression         sense              4     1
7892502
6    2  7892502 expression         sense              4     1
7892502
 groupDirection groupNbrOfAtoms    cell   x   y pbase tbase indexPos
atom
1          sense               4  116371 870 110     C     G
0    0
2          sense               4  943979  28 899     A     T
1    1
3          sense               4  493089 638 469     T     A
2    2
4          sense               4  907039 888 863     A     T
3    3
5          sense               4 1033309 108 984     T     A
0    0
6          sense               4  653512 411 622     T     A
1    1

I'm not sure what object you have in mind when it comes to a probe-
intensity pair, but this should give you all the info you might want
(e.g. cell index, x/y physical location).

HTH,
Mark


On Aug 9, 5:45 pm, Pierre Neuvial <pie...@stat.berkeley.edu> wrote:
> Hi,
>
> Have you tried using extractAffyBatch, which is documented 
> here:http://aroma-project.org/howtos/extractAffyBatch?
> As far as I understand you will need the Bioconductor annotation
> package corresponding to your chip type to be installed, ie
>
>  source("http://www.bioconductor.org/biocLite.R";)
>  biocLite("hgu133plus2cdf")
>
> This is discussed in this 
> thread:http://groups.google.com/group/aroma-affymetrix/browse_thread/thread/...
>
> Pierre
>
> On Tue, Aug 9, 2011 at 4:34 AM, hsingjun cheung
>
>
>
>
>
>
>
> <hsingjun.ch...@gmail.com> wrote:
> > Hi Pierre:
>
> > Thanks. These functions work now. Do you know how to extract the raw
> > intensity for each probe ?
>
> > On Aug 8, 5:48 pm, Pierre Neuvial <pie...@stat.berkeley.edu> wrote:
> >> Hi,
>
> >> The 'annotationData' directory should be directly in your working
> >> directory, as explained in the page "Setup: Location of annotation
> >> data files":http://aroma-project.org/node/66
>
> >> In your case, you need to change the current directory to ~/experiment/ by
>
> >> setwd("~/experiment/")
>
> >> (or by starting your R session from this directory).  Then your command
>
> >> csR <- AffymetrixCelSet$byName("KN01M013",chipType="HG-U133_Plus_2")
>
> >> should work.
>
> >> Best,
>
> >> Pierre
>
> >> On Mon, Aug 8, 2011 at 5:29 PM, hsingjun cheung
>
> >> <hsingjun.ch...@gmail.com> wrote:
> >> > Hello:
>
> >> > I searched the group but got no results ... So I want to know, how to
> >> > extract the raw probe intensity from .CEL file?
>
> >> > The file structure on my computer is like:
>
> >> > ~/experiemnt/
> >> >             annotationData/
> >> >                         chipTypes/
> >> >                                HG-U133_Plus_2/
> >> >                                           HG-U133_Plus_2.cdf
> >> > ~/experiment/
> >> >               rawData/
> >> >                       KN01M013/
> >> >                               HG-U133_Plus_2/
> >> >                                                    KN01M013.CEL
>
> >> > The .cdf file is downloaded 
> >> > fromhttp://www.aroma-project.org/chipTypes/HG-U133_Plus_2
>
> >> > When I run R under ~ directory:
> >> > library(aroma.affymetrix)
> >> >  csR <- AffymetrixCelSet$byName("KN01M013",chipType="HG-U133_Plus_2")
>
> >> > I got error msg:
>
> >> > Error in list(`AffymetrixCelSet$byName("KN01M013", chipType = "HG-
> >> > U133_Plus_2")` = <environment>,  :
>
> >> > [2011-08-08 11:24:05] Exception: Could not locate a file for this chip
> >> > type: HG-U133_Plus_2
> >> >  at throw(Exception(...))
> >> >  at throw.default("Could not locate a file for this chip type: ",
> >> > paste(c(chipT
> >> >  at throw("Could not locate a file for this chip type: ",
> >> > paste(c(chipType, tag
> >> >  at method(static, ...)
> >> >  at AffymetrixCdfFile$byChipType(chipType)
> >> >  at method(static, ...)
> >> >  at AffymetrixCelSet$byName("KN01M013", chipType = "HG-U133_Plus_2")
>
> >> > Could anyone help me figure how this error happened ? And how to do
> >> > it  ( extract raw probe intensity ) in a right way ? Thanks
>
> >> > --
> >> > 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 "aroma.affymetrix" group with 
> >> > websitehttp://www.aroma-project.org/.
> >> > To post to this group, send email to aroma-affymetrix@googlegroups.com
> >> > To unsubscribe and other options, go 
> >> > tohttp://www.aroma-project.org/forum/
>
> > --
> > 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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-- 
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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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