[BioC] print layout for Agilent data?
Jianping Jin
jjin at email.unc.edu
Tue Oct 30 15:50:02 CET 2007
Thanks Sean.
Here back to my original questions. Reading in data with "read.maimages"
had no problems (see below)
> RG$genes[1:5,]
Row Col Start Sequence ProbeUID ControlType ProbeName
GeneName
1 1 1 0 0 1 GE_BrightCorner
GE_BrightCorner
2 1 2 0 1 1 DarkCorner
DarkCorner
3 1 3 0 1 1 DarkCorner
DarkCorner
4 1 4 0 1 1 DarkCorner
DarkCorner
5 1 5 0 1 1 DarkCorner
DarkCorner
SystematicName Description
1 GE_BrightCorner
2 DarkCorner
3 DarkCorner
4 DarkCorner
5 DarkCorner
But when I was trying the normalizeWithinArrays function I got an error:
Error in switch (method, loess= {: Layout argument not specified).
As you can see the RG file has already taken in the Row and Col
information. There is no Block column however, as Agilent array has not
designed as different blocks. That may be the reason of the error. I wanted
to know how people handle this situation in order to carry out loess
normalization for each array. Do we need to add a "Block" column into
RG$genes or specify gene layout format?
best,
JJ-
--On Tuesday, October 30, 2007 10:12 AM -0400 Sean Davis
<sdavis2 at mail.nih.gov> wrote:
> Jianping Jin wrote:
>> Hi John,
>>
>> This is my first to handle the Agilent 4x44k arrays. Yes you are right.
>> My collaborator ran 9 chips and sent me 36 separate files. For
>> "read.maimages" they should serve as individual data files to read in
>> just like regular arrays. Am I right? Is there any other file(s) which
>> need to be read in?
>
> That should do it.
>
> Sean
##################################
Jianping Jin Ph.D.
Bioinformatics scientist
Center for Bioinformatics
Room 3133 Bioinformatics building
CB# 7104
University of Chapel Hill
Chapel Hill, NC 27599
Phone: (919)843-6105
FAX: (919)843-3103
E-Mail: jjin at email.unc.edu
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