[BioC] print layout for Agilent data?
Sean Davis
sdavis2 at mail.nih.gov
Tue Oct 30 17:03:25 CET 2007
Jianping Jin wrote:
> Great Sean! You solved my problem.
>
> Do you know an easy way to remove all Agilent control spots, including
> empty, negative and positive controls from a gene list to be analyzed.
I believe the controltype column contains these information. You can
just remove probes with controltype!=0, if I recall correctly.
> --On Tuesday, October 30, 2007 10:54 AM -0400 Sean Davis
> <sdavis2 at mail.nih.gov> wrote:
>
>> Jianping Jin wrote:
>>> 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).
>>
>> Reading the help for normalizeWithinArrays, you might notice that the
>> default method is "printtiploess". That is fine, except that you need
>> to specify the layout by hand. However, Agilent does not use "print
>> tips" or blocks, so printtiploess is not appropriate for Agilent arrays.
>> I think if you specify method="loess", you will probably find that
>> things work just fine.
>>
>> Sean
>
>
>
> ##################################
> Jianping Jin Ph.D.
> Bioinformatics scientist
> Center for Bioinformatics
> Room 3133 Bioinformatics building
> CB# 7104, Campus
> Phone: (919)843-6105
> FAX: (919)843-3103
> E-Mail: jjin at unc.edu
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