Moreover, chrom 1 and 2, in all samples, seems not to have been done, (in
grey shade when browsing acrross chromosomes and samples.
Myriam

-----Original Message-----
From: Myriam Peyrard [mailto:myriam.peyr...@ki.se] 
Sent: den 11 juni 2009 10:09
To: 'aroma-affymetrix@googlegroups.com'
Subject: RE: [aroma.affymetrix] Re: CNV analys 28 st SNP 6.0 arrays
Importance: High

OK, nice to hear, about the warnings.
Then  I do:
display(ce)
and started to look in my different samples, all chromosomes.
Seems that there is not a single CNV variation there?
I did the normalization as non-paired sample sets, with average calculated
with all samples:

cbs <- CbsModel(cesN)

Is this a normal output? I expected to have many variations and to have to
sort them out in different ways. Now, I think something has gone wrong
instead. Any ideas?

Myriam

-----Original Message-----
From: aroma-affymetrix@googlegroups.com
[mailto:aroma-affymet...@googlegroups.com] On Behalf Of Henrik Bengtsson
Sent: den 11 juni 2009 09:38
To: aroma-affymetrix@googlegroups.com
Subject: [aroma.affymetrix] Re: CNV analys 28 st SNP 6.0 arrays


Hi.

On Thu, Jun 11, 2009 at 12:29 AM, Myriam <myriam.peyr...@ki.se> wrote:
>
> Dear all,
>
> I have gone through a number of steps in the analysis of 28 arrays of
> the Genomewide6.0 type and all seems OK until now:
>
> #Fitting copy-number model and displaying results
> #######################################################################
> ce <- ChromosomeExplorer(cbs)
> ce
>
> #ChromosomeExplorer:
> #Name: CLP
> #Tags: ACC,ra,-XY,AVG,+300,A+B,FLN,-XY
> #Number of arrays: 28
> #Path: reports/CLP/ACC,ra,-XY,AVG,+300,A+B,FLN,-XY/GenomeWideSNP_6/cbs
> #RAM: 0.00MB
>
> process(ce, chromosomes=c
> (1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23),
> verbose=verbose)

FYI, you can write the above much shorter:

  process(ce, chromosomes=1:23, verbose=verbose)

>
> And the end of the output after many hours run, looks like this:
> #20090610 02:17:03| Writing CN regions...done
> #20090610 02:17:03|Generating ChromosomeExplorer report...done
> #[1] TRUE
> #There were 50 or more warnings (use warnings() to see the first 50)
>
> I am looking at the 50 first warnings and I see that many are of the
> same type. here comes an example of one of the each category of
> warning. What shall I do now with each of those?

You don't have to do anything.  These warnings are alright and
expected.  No worries here.  If you on the other hand get *errors*
then you have to worry, but those will halt the script immediately.

/Henrik

> 1: In library(package, lib.loc = lib.loc, character.only =
> TRUE,  ... :
>  there is no package called 'Cairo'
> 2: In method(static, ...) :
>  Ghostscript not found. Searched directories: C:/gs, C:\Program/gs, /
> gs, C:\Program\Delade filer/gs
> 3: In DNAcopy::CNA(genomdat = data$y, chrom = data$chromosome,  ... :
>  array has repeated maploc positions
>
> 4: In plotDev(pathname, width = width, height = height) :
>  Unable to allocate bitmap
> 5: In plotDev(pathname, width = width, height = height) : opening
> device failed
> 6: In log(theta/thetaRef, base = 2) : NaNs produced
> 7: In log(theta * thetaRef, base = 2) : NaNs produced
> 8: In DNAcopy::CNA(genomdat = data$y, chrom = data$chromosome,  ... :
>  array has repeated maploc positions
>
> Thanks a lot in adavnce for any help!
> Myriam
>
>
>
>
>
>
> >





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