Re: [aroma.affymetrix] Re: How to extract raw probe intensity from .CEL file

2011-08-09 Thread Mark Robinson

How about grabbing the intensities according to their index:

raw=extractMatrix(cs,cells=df$cell,verbose=verbose)

Then you'll have them matched up to the 'df' data.frame.

(Different numbers for your chip, of course)
> dim(df)
[1] 844550 16
> dim(raw)
[1] 844550 33


Mark

On Aug 10, 2011, at 12:31 AM, hsingjun cheung wrote:

> Hi Mark:
> 
> My idea is how we could know the intensity for each probe ? Using
> these command:
> library(aroma.affymetrix)
> cs <- AffymetrixCelSet$byName("KN01M013", chipType="HG-U133_Plus_2")
> raw=extractMatrix(cs,verbose=verbose)
> 
> I can see 'raw' is a list of intensities, but I don't know which probe
> ids they correspond to.  Hope this clarifies. Thanks
> 
> On Aug 9, 6:03 am, Mark Robinson  wrote:
>> 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
>> 11  7892501 expression sense  4 1
>> 7892501
>> 21  7892501 expression sense  4 1
>> 7892501
>> 31  7892501 expression sense  4 1
>> 7892501
>> 41  7892501 expression sense  4 1
>> 7892501
>> 52  7892502 expression sense  4 1
>> 7892502
>> 62  7892502 expression sense  4 1
>> 7892502
>>  groupDirection groupNbrOfAtomscell   x   y pbase tbase indexPos
>> atom
>> 1  sense   4  116371 870 110 C G
>> 00
>> 2  sense   4  943979  28 899 A T
>> 11
>> 3  sense   4  493089 638 469 T A
>> 22
>> 4  sense   4  907039 888 863 A T
>> 33
>> 5  sense   4 1033309 108 984 T A
>> 00
>> 6  sense   4  653512 411 622 T A
>> 11
>> 
>> 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  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
>> 
>>>  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  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
>> 
>  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")` = ,  :
>> 
>> [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(sta

Re: [aroma.affymetrix] Re: How to extract raw probe intensity from .CEL file

2011-08-09 Thread Pierre Neuvial
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/40e3950e52d73c1f/772e387a3163db56

Pierre

On Tue, Aug 9, 2011 at 4:34 AM, hsingjun cheung
 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  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$byName("KN01M013",chipType="HG-U133_Plus_2")
>>
>> should work.
>>
>> Best,
>>
>> Pierre
>>
>> On Mon, Aug 8, 2011 at 5:29 PM, hsingjun cheung
>>
>>
>>
>>
>>
>>
>>
>>  wrote:
>> > Hello:
>>
>> > I searched the group but got no results ... So I want to know, how to
>> > extract the raw probe intensity from .CEL file?
>>
>> > The file structure on my computer is like:
>>
>> > ~/experiemnt/
>> >             annotationData/
>> >                         chipTypes/
>> >                                HG-U133_Plus_2/
>> >                                           HG-U133_Plus_2.cdf
>> > ~/experiment/
>> >               rawData/
>> >                       KN01M013/
>> >                               HG-U133_Plus_2/
>> >                                                    KN01M013.CEL
>>
>> > The .cdf file is downloaded 
>> > fromhttp://www.aroma-project.org/chipTypes/HG-U133_Plus_2
>>
>> > When I run R under ~ directory:
>> > library(aroma.affymetrix)
>> >  csR <- AffymetrixCelSet$byName("KN01M013",chipType="HG-U133_Plus_2")
>>
>> > I got error msg:
>>
>> > Error in list(`AffymetrixCelSet$byName("KN01M013", chipType = "HG-
>> > U133_Plus_2")` = ,  :
>>
>> > [2011-08-08 11:24:05] Exception: Could not locate a file for this chip
>> > type: HG-U133_Plus_2
>> >  at throw(Exception(...))
>> >  at throw.default("Could not locate a file for this chip type: ",
>> > paste(c(chipT
>> >  at throw("Could not locate a file for this chip type: ",
>> > paste(c(chipType, tag
>> >  at method(static, ...)
>> >  at AffymetrixCdfFile$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.
>>
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>
> --
> 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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>

-- 
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.


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