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Heidi Dvinge
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@heidi-dvinge-5340
Last seen 10.3 years ago
Hi Silvia,
On 15 Jun 2012, at 18:45, Silvia Halim wrote:
> Hi Heidi,
>
> I ran into below problem when using plotCtReps.
>
> > plotCtReps(temp, card = 1, percent = 20, xlim = c(0,50), ylim =
c(0,50))
> Error in split.data[[s]] : subscript out of bounds
> In addition: Warning messages:
> 1: In min(x, na.rm = na.rm) :
> no non-missing arguments to min; returning Inf
> 2: In max(x, na.rm = na.rm) :
> no non-missing arguments to max; returning -Inf
> > plotCtReps(temp, card = 1, percent = 20, xlim = c(0,50), ylim =
c(0,50))
> Error in split.data[[s]] : subscript out of bounds
> In addition: Warning messages:
> 1: In min(x, na.rm = na.rm) :
> no non-missing arguments to min; returning Inf
> 2: In max(x, na.rm = na.rm) :
> no non-missing arguments to max; returning -Inf
> > plotCtReps(temp, card = 2, percent = 20, xlim = c(0,100), ylim =
c(0,100))
> Error in split.data[[s]] : subscript out of bounds
> In addition: Warning messages:
> 1: In min(x, na.rm = na.rm) :
> no non-missing arguments to min; returning Inf
> 2: In max(x, na.rm = na.rm) :
> no non-missing arguments to max; returning -Inf
What's the output from traceback(), i.e. exactly where does the
function break?
>
A couple of things you can try:
- plotCtReps is meant to be used in cases where there are exactly 2
replicates of the features on your assay. Is this the case? For
example, with the data below there are 190 features that will be
plotted, and 1 that will be skipped:
> data(qPCRraw)
> table(table(featureNames(qPCRraw)))
2 4
190 1
- are there any NAs in your data? E.g. sumis.na(qPCRraw))>0.
HTH
\Heidi
> Here is how ?temp? looks like
> > temp
> An object of class "qPCRset"
> Size: 96 features, 96 samples
> Feature types: Reference, Test
> Feature names: b-Actin b-Actin b-Actin ...
> Feature classes:
> Feature categories: OK
> Sample names: NTC_4 PMPT352 NTC_3 ...
>
> Do you know why it is complaining about split.data?
>
> Thanks,
> Silvia
>
> -----Original Message-----
> From: Heidi Dvinge
> Sent: 11 June 2012 6:11 PM
> To: Silvia Halim
> Subject: Re: HTqPCR
>
> Ok, so you already have a 96 by 96 matrix, so you don't need
changeCtLayout.
> Good luck with the rest, and let me know if you encounter any
problems.
>
> On 11 Jun 2012, at 19:05, Silvia Halim wrote:
>
> > Hi Heidi,
> >
> > Thank you for your clarification.
> >
> > Btw this is how it looks like when I type 'temp'
> >> temp
> > An object of class "qPCRset"
> > Size: 96 features, 96 samples
> > Feature types: Reference, Test
> > Feature names: b-Actin b-Actin b-Actin ...
> > Feature classes:
> > Feature categories: OK
> > Sample names: NTC_4 PMPT352 NTC_3 ...
> >
> > Cheers,
> > Silvia
> >
> > -----Original Message-----
> > From: Heidi Dvinge
> > Sent: 08 June 2012 7:12 PM
> > To: Silvia Halim
> > Subject: Re: HTqPCR
> >
> > Hi Silvia,
> >
> > what are the dimensions of the "temp" object that you read in?
I.e.
> > what does it look like if you just type
> >> temp
> >
> > If you read in the data with n.features=96 and n.data=96, then you
should already have an object with 96 rows and 96 columns, in which
case you don't need to change the layout.
> >
> > Best,
> > \Heidi
> >
> > On 8 Jun 2012, at 19:13, Silvia Halim wrote:
> >
> >> Hi Heidi,
> >>
> >> I finally have time to try out your HTqPCR bioconductor package
again and I was trying to use 'changeCtLayout' function. However, I
got following error message:
> >>
> >>> qPCRnew <- changeCtLayout(temp, sample.order = sample_order)
> >> Error in data.frame(..., check.names = FALSE) :
> >> arguments imply differing number of rows: 0, 96 In addition:
Warning
> >> message:
> >> In split.default(x = seq_len(nrow(x)), f = f, drop = drop, ...) :
> >> data length is not a multiple of split variable
> >>
> >> The commands that I run are as follows:
> >>> temp <- readCtData("110614 BENIGN_1 DATA 96X96.csv", path =
getwd(),
> >>> n.features = 96, n.data=96, flag = 9, feature = 5, type= 6, Ct =
7,
> >>> position = 1, skip = 12, sep = ",") sample_order <-
> >>> rep(sampleNames(temp), each = 96) qPCRnew <-
changeCtLayout(temp,
> >>> sample.order = sample_order)
> >>
> >> I've tried to follow what's written in changeCtLayout function
description. Can you please advise what went wrong?
> >>
> >> Thanks,
> >> Silvia
> >>
> >> -----Original Message-----
> >> From: Heidi Dvinge
> >> Sent: 29 April 2012 8:18 PM
> >> To: Silvia Halim
> >> Subject: Re: HTqPCR
> >>
> >> HI Silvia,
> >>
> >> I'm glad you got it working. Depending on what you're supposed to
do with the data, you may need to tweak some functions slightly, as
you mention. Let me know if you run into any more trouble.
> >>
> >> Cheers
> >> \Heidi
> >>
> >> On 26 Apr 2012, at 18:37, Silvia Halim wrote:
> >>
> >>> Hi Heidi,
> >>>
> >>> Thanks for the help! It's working for me now. Right now I'm
figuring it out how I can use the functions that you described in the
vignette. I might have to tweak the parameters for using the functions
on Fluidigm data.
> >>>
> >>> Cheers,
> >>> Silvia
> >>>
> >>> -----Original Message-----
> >>> From: Heidi Dvinge
> >>> Sent: 25 April 2012 8:56 AM
> >>> To: Silvia Halim
> >>> Subject: Re: HTqPCR
> >>>
> >>> Hiya,
> >>>
> >>> sorry, I only just now realised that you'd attached a file. When
I saved as csv, the following command worked:
> >>>
> >>>> raw <- readCtData("110614 BENIGN_1 DATA 96x96.csv",
> >>>> format="BioMark",
> >>>> n.features=96*96) raw
> >>> An object of class "qPCRset"
> >>> Size: 9216 features, 1 samples
> >>> Feature types:
> >>> Feature names: b-Actin b-Actin
b-Actin ...
> >>> Feature classes:
> >>> Feature categories: OK
> >>> Sample names: 110614
BENIGN_1 DATA 96x96 ...
> >>>
> >>> The data isn't transformed into a 96x96 format immediately
though (in case you read in multiple arrays, and want to normalise
them independently). If you want to change this, you can use
changeCtLayout(). Alternatively you can say:
> >>>
> >>>> raw <- readCtData("110614 BENIGN_1 DATA 96x96.csv",
> >>>> format="BioMark", n.features=96, n.data=96) raw
> >>> An object of class "qPCRset"
> >>> Size: 96 features, 96 samples
> >>> Feature types:
> >>> Feature names: b-Actin b-Actin
b-Actin ...
> >>> Feature classes:
> >>> Feature categories: OK
> >>> Sample names:
Sample1 Sample2 Sample3 ...
> >>>> plotCtArray(raw)
> >>>
> >>> HTH
> >>> \Heidi
> >>>
> >>> On 24 Apr 2012, at 17:55, Silvia Halim wrote:
> >>>
> >>>> Hi Heidi,
> >>>>
> >>>> I have some problems updating R on lustre. Therefore, I chose
to run HTqPCR on my desktop for the moment.
> >>>>
> >>>> Reading in your sample file looks fine, however, reading in the
> >>>> file that I showed you just now gave me below error message.
(The
> >>>> file is as attached)
> >>>>
> >>>>> temp <- readCtData("110614 BENIGN_1 DATA 96x96.xlsx", path =
> >>>>> getwd() , n.features = 96*96, flag = 9, feature = 5, type= 6,
Ct =
> >>>>> 7,position = 1, skip = 12, sep = ",")
> >>>> Error in read.table(file = file, header = header, sep = sep,
quote = quote, :
> >>>> no lines available in input
> >>>> In addition: Warning message:
> >>>> In readLines(file, skip) :
> >>>> incomplete final line found on
'C:/Users/halim01/Documents/20110627_RossAdamsH_DN_Fluid/110614
BENIGN_1 DATA 96x96.xlsx'
> >>>>> sessionInfo()
> >>>> R version 2.14.0 (2011-10-31)
> >>>> Platform: x86_64-pc-mingw32/x64 (64-bit)
> >>>>
> >>>> locale:
> >>>> [1] LC_COLLATE=English_United Kingdom.1252
LC_CTYPE=English_United Kingdom.1252 LC_MONETARY=English_United
Kingdom.1252 LC_NUMERIC=C
LC_TIME=English_United Kingdom.1252
> >>>>
> >>>> attached base packages:
> >>>> [1] stats graphics grDevices utils datasets methods
base
> >>>>
> >>>> other attached packages:
> >>>> [1] Biostrings_2.22.0 IRanges_1.12.6 BiocInstaller_1.2.1
marray_1.32.0 HTqPCR_1.8.0 limma_3.10.3
RColorBrewer_1.0-5 Biobase_2.14.0 gdata_2.8.2
> >>>>
> >>>> loaded via a namespace (and not attached):
> >>>> [1] affy_1.32.1 affyio_1.22.0 gplots_2.10.1
gtools_2.6.2 preprocessCore_1.16.0 tools_2.14.0
zlibbioc_1.0.1
> >>>>>
> >>>>
> >>>> I did a quick check on the file and it only has 9228 lines
including 12 header lines which I had skipped when reading in the
file. Do you know what could possibly go wrong?
> >>>>
> >>>> Cheers,
> >>>> Silvia
> >>>>
> >>>> -----Original Message-----
> >>>> From: Heidi Dvinge
> >>>> Sent: 24 April 2012 5:09 PM
> >>>> To: Silvia Halim
> >>>> Subject: Re: HTqPCR
> >>>>
> >>>> Hm, that looks like it may be x11 acting up. I often have
similar issues when I work on a remote server.
> >>>>
> >>>> Actually, the processing of Fluidigm files is very
computationally light. So you can easily do it on your desktop, if you
can't update on lustre.
> >>>>
> >>>> I can also email you and older version of the vignette if you
want to have a look. However, in HTqPCR 1.2.0 I don't even think I had
a dedicated function for plotting the Fluidigm assays yet (the
plotCtArray shown in the vignette).
> >>>>
> >>>> Cheers
> >>>> \Heidi
> >>>>
> >>>> On 24 Apr 2012, at 16:39, Silvia Halim wrote:
> >>>>
> >>>>> Hi Heidi,
> >>>>>
> >>>>> This is what I got when accessing the vignette.
> >>>>>
> >>>>>> openVignette(package="HTqPCR")
> >>>>> Please select a vignette:
> >>>>>
> >>>>> 1: HTqPCR - qPCR analysis in R
> >>>>>
> >>>>> Selection: 1
> >>>>> Opening /home/mib-
cri/local/lib64/R/library/HTqPCR/doc/HTqPCR.pdf
> >>>>>> xprop: unable to open display ''
> >>>>> /usr/local/bin/xdg-open: line 370: firefox: command not found
> >>>>> /usr/local/bin/xdg-open: line 370: mozilla: command not found
> >>>>> /usr/local/bin/xdg-open: line 370: netscape: command not found
> >>>>> xdg-open: no method available for opening '/home/mib-
cri/local/lib64/R/library/HTqPCR/doc/HTqPCR.pdf'
> >>>>>
> >>>>> Sorry for the confusion, you are right that I was looking at a
newer version of HTqPCR than the one installed on lustre. I think
that's because I have different installations of HTqPCR on lustre and
on my desktop. If I can update the one on lustre, I'll go ahead with
the update.
> >>>>>
> >>>>> Thank you,
> >>>>> Silvia
> >>>>>
> >>>>> -----Original Message-----
> >>>>> From: Heidi Dvinge
> >>>>> Sent: 24 April 2012 4:28 PM
> >>>>> To: Silvia Halim
> >>>>> Subject: Re: HTqPCR
> >>>>>
> >>>>> Ah, right, it looks like you have an older version of R, and
therefore also HTqPCR.
> >>>>>
> >>>>> The most current release version is 1.10.0. In that version,
readCtData() was modified to accept different types of input data,
including from Fluidigm. Before that, this sort of data had to be read
in 'manually'.
> >>>>>
> >>>>> I guess the vignette that you were looking at comes from a
version
> >>>>> of HTqPCR that's newer than the one you have installed? If you
> >>>>> access the vignette corresponding to your HTqPCR version via
> >>>>>> openVignette(package="HTqPCR")
> >>>>> what do you get then?
> >>>>>
> >>>>> If you get an older version, then depending on how old it is,
there may be a section towards the end giving an example of how to
process Fluidigm data more 'manually'. If not, an update may be your
best bet.
> >>>>>
> >>>>> Cheers
> >>>>> \Heidi
> >>>>>
> >>>>>
> >>>>>
> >>>>> On 24 Apr 2012, at 16:15, Silvia Halim wrote:
> >>>>>
> >>>>>> Hi Heidi,
> >>>>>>
> >>>>>> Thanks for looking into the matter. Below is the output of
my
> >>>>>> sessionInfo()
> >>>>>>
> >>>>>>> sessionInfo()
> >>>>>> R version 2.13.0 (2011-04-13)
> >>>>>> Platform: x86_64-unknown-linux-gnu (64-bit)
> >>>>>>
> >>>>>> 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] marray_1.26.0 Biostrings_2.20.1 IRanges_1.10.3
HTqPCR_1.2.0
> >>>>>> [5] limma_3.6.9 RColorBrewer_1.0-2 Biobase_2.12.1
gdata_2.8.0
> >>>>>>
> >>>>>> loaded via a namespace (and not attached):
> >>>>>> [1] affy_1.26.1 affyio_1.20.0 gplots_2.8.0
> >>>>>> [4] gtools_2.6.2 preprocessCore_1.14.0
> >>>>>>>
> >>>>>>
> >>>>>> Cheers,
> >>>>>> Silvia
> >>>>>>
> >>>>>> -----Original Message-----
> >>>>>> From: Heidi Dvinge
> >>>>>> Sent: 24 April 2012 4:07 PM
> >>>>>> To: Silvia Halim
> >>>>>> Subject: HTqPCR
> >>>>>>
> >>>>>> Hi Silvia,
> >>>>>>
> >>>>>> I just tested the read fluidigm from the vignette, and it
works on both my mac and a single unix system that I've tested.
Although from the errors you were getting, it seemed like the headers
weren't been read correctly/at all.
> >>>>>>
> >>>>>> Would you mind sending me the output of your sessionInfo(),
so I can compare which package versions we have?
> >>>>>>
> >>>>>> Best,
> >>>>>> \Heidi
> >>>>>>
> >>>>>>> sessionInfo()
> >>>>>> R version 2.15.0 (2012-03-30)
> >>>>>> Platform: x86_64-apple-darwin9.8.0/x86_64 (64-bit)
> >>>>>>
> >>>>>> locale:
> >>>>>> [1]
en_GB.UTF-8/en_GB.UTF-8/en_GB.UTF-8/C/en_GB.UTF-8/en_GB.UTF-8
> >>>>>>
> >>>>>> attached base packages:
> >>>>>> [1] tools stats graphics grDevices utils
datasets methods base
> >>>>>>
> >>>>>> other attached packages:
> >>>>>> [1] HTqPCR_1.10.0 limma_3.12.0 RColorBrewer_1.0-5
Biobase_2.16.0
> >>>>>> [5] BiocGenerics_0.2.0
> >>>>>>
> >>>>>> loaded via a namespace (and not attached):
> >>>>>> [1] affy_1.34.0 affyio_1.24.0
BiocInstaller_1.4.3
> >>>>>> [4] gdata_2.8.2 gplots_2.10.1 gtools_2.6.2
> >>>>>> [7] preprocessCore_1.18.0 stats4_2.15.0
zlibbioc_1.2.0
> >>>>>>
> >>>>>>
> >>>>>
> >>>>
> >>>> <110614 BENIGN_1 DATA 96x96.xlsx>
> >>>
> >>
> >
>
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