[BioC] HTqPCR only works for 384 qPCR plates
axel.klenk at actelion.com
axel.klenk at actelion.com
Wed Apr 21 19:44:31 CEST 2010
Dear Andreia,
again, have a look at the help page. It will tell you that
readCtData() has certain expectations about the number
of certain columns, ie.
flag = 4, feature = 6, type = 7, position = 3, Ct = 8
If your files have that information in a different column,
you'll have to specify the column number, if they do not
have it at all you'll have to set it to NULL, as explained
in the Details section.
In your case the function was looking for columns number
3, 4, 6, 7 and 8 in a file with only two or three columns
which explains the error message.
Cheers,
- axel
Axel Klenk
Research Informatician
Actelion Pharmaceuticals Ltd / Gewerbestrasse 16 / CH-4123 Allschwil /
Switzerland
Andreia Fonseca
<andreia.fonseca@
gmail.com> To
axel.klenk at actelion.com
04/21/2010 07:06 cc
PM bioconductor
<bioconductor at stat.math.ethz.ch>,
bioconductor-bounces at stat.math.ethz
.ch
Subject
Re: [BioC] HTqPCR only works for
384 qPCR plates
Dear Axel,
I have tried and now I have another error i think is due to my
files: raw<-readCtData(files=files$File, path=path, n.features=80)
Error in `[.data.frame`(sample, , Ct) : undefined columns selected
so in my files I have
gene \t Ctvalue
gene \t Ctvalue \t type(target/endogenous)
should I have a column with the sample number and the condition too?
thanks
Andreia
On Wed, Apr 21, 2010 at 5:54 PM, <axel.klenk at actelion.com> wrote:
Dear Andreia,
not exactly, it only expects 384 plates...
Try
?readCtData
and consequently:
raw<-readCtData(files=files$File, path=path, n.features=80)
Cheers, - axel
Axel Klenk
Research Informatician
Actelion Pharmaceuticals Ltd / Gewerbestrasse 16 / CH-4123 Allschwil /
Switzerland Andreia Fonseca
<andreia.fonseca@ gmail.com
> To Sent
by: bioconductor bioconductor-boun <
bioconductor at stat.math.ethz.ch>
ces at stat.math.eth cc
z.ch
Subject [BioC] HTqPCR only works for
384 04/21/2010 06:29 qPCR plates PM
Dear all,
I have data for 80 miRNAs produced with qPCR plates, I am trying to use
HTqPCR but I am receiving an error, due to this. bellow is the error
message
and the session info.
thanks
regards,
Andreia
> raw<-readCtData(files=files$File, path=path)
Error in readCtData(files = files$File, path = path) : 384 gene names
(rows) expected, got 80
> sessionInfo()
R version 2.10.1 (2009-12-14)
x86_64-pc-linux-gnu
locale: [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C [3]
LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8 [5]
LC_MONETARY=C LC_MESSAGES=en_US.UTF-8 [7]
LC_PAPER=en_US.UTF-8 LC_NAME=C [9] LC_ADDRESS=C
LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] qpcrNorm_1.4.0 affy_1.24.2 HTqPCR_1.0.0
limma_3.2.1
[5] RColorBrewer_1.0-2 Biobase_2.6.1
loaded via a namespace (and not attached):
[1] affyio_1.14.0 gdata_2.7.1 gplots_2.7.4
[4] gtools_2.6.1 preprocessCore_1.8.0 tools_2.10.1
--
--------------------------------------------
Andreia J. Amaral
Unidade de Imunologia Clínica
Instituto de Medicina Molecular
Universidade de Lisboa
email: andreiaamaral at fm.ul.pt
andreia.fonseca at gmail.com
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--
--------------------------------------------
Andreia J. Amaral
Unidade de Imunologia Clínica
Instituto de Medicina Molecular
Universidade de Lisboa
email: andreiaamaral at fm.ul.pt
andreia.fonseca at gmail.com
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It is intended solely for the addressee. If you are not the intended recipient, any copying, distribution or any other use of this email is prohibited and may be unlawful. In such case, you should please notify the sender immediately and destroy this email.
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