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Nataliya Yeremenko
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100
@nataliya-yeremenko-1481
Last seen 10.2 years ago
Dear members of the Bioconductor mail-list
dear maintainers of the limma and marray packages
I wonder if there is proper handling of the Agilent 44K arrays is
implemented in marray.
Meanwhile I'm analyzing my human 44K in limma,
and everything works fine with a great help of the list and almost
perfect userguide
(I'm rather biologist, than bioinformatician).
Than the question appears to try "globalMAD" normalization from
marray.
Excited with limma userguide words about easy conversion of the RGlist
data to marrayRaw object.
I started in LIMMA like this:
>RG.raw <- read.maimages(files = targets$fileName, path = loadPath,
source = "agilent", quote="")
...
>dim(RG.raw)
[1] 43931 29
>RG.raw$genes$Status <- controlStatus(spottypes, RG.raw)
Matching patterns for: ControlType
Found 43931 Probe
Found 314 Negative
Found 1942 Positive
Setting attributes: values Color
SEEMS FINE so far
> data.raw <- as(RG.raw, "marrayRaw")
> summary(data.raw)
...
A) Layout of spots on the array:
Array layout: Object of class marrayLayout.
Total number of spots: Dimensions of grid
matrix: rows by cols
Dimensions of spot matrices: rows by cols
Currently working with a subset of spots.
Control spots:
There are 3 types of controls :
Negative Positive Probe
314 1942 41675
Notes on layout:
...
> data.norm <- maNorm(data.raw,norm="loess",echo=TRUE)
Normalization method: loess.
Normalizing array 1.
Error in if is.int(totalPlate)) { : argument is of length zero
OOPS :) Petty, It seems that marrayLayout is wrong.
Than I thought that import of the data is implemented better than the
conversion in marray I tried in frame of MARRAY:
> data.marray.raw <- read.Agilent(fnames=targets$fileName, quote="")
> summary(data.marray.raw)
...
A) Layout of spots on the array:
Array layout: Object of class marrayLayout.
Total number of spots: 12900
Dimensions of grid matrix: 1 rows by 1 cols
Dimensions of spot matrices: 30 rows by 430 cols
Currently working with a subset of 12797spots.
Control spots:
There are 3 types of controls :
Negative Positive probes
47 311 5837
Notes on layout:
ONCE again, something wrong with layout
However maNorm() is working w/o reported mistakes,
but I wonder what is it normalising...
Does anybody have any clue how to deal with Agilent 44K within
marray?
I searched for the archive, and did find the rare discussions on this,
but didn't find the answer.
I wonder as well if this problem is fixed in the developing version of
the MARRAY
And finaly, as advised below is
> sessionInfo()
R version 2.2.1, 2005-12-20, i386-pc-mingw32
attached base packages:
[1] "tools" "methods" "stats" "graphics" "grDevices"
"utils" "datasets" "base"
other attached packages:
convert marray vsn Biobase gplots gdata gtools limma
"1.4.0" "1.8.0" "1.8.0" "1.8.0" "2.3.0" "2.1.2" "2.2.3" "2.4.13"
>
Waiting for advices...
--
--
Dr. Nataliya Yeremenko
Universiteit van Amsterdam
Faculty of Science
IBED/AMB (Aquatische Microbiologie)
Nieuwe Achtergracht 127
NL-1018WS Amsterdam
the Netherlands
tel. + 31 20 5257089
fax + 31 20 5257064