[BioC] bugs in arrayQuality and marray
Francois Pepin
fpepin at cs.mcgill.ca
Sat Dec 3 01:06:11 CET 2005
Hi everyone,
I've hit a couple of bugs while trying out arrayQuality (downloaded from
ucsf site, they have an earlier version than bioconductor) for my
Agilent arrays.
read.Agilent, from the marray package, is ignoring the 'path' parameter
when 'fnames' is given:
if (is.null(fnames)) {
...
}
else fullnames <- fnames
The readAgilent function, from the arrayQuality package, has problems
with the skip parameter. First of all, it is completely ignored:
skip <- grep("gMedianSignal", y)[1]
Then lower down, it is incorrectly offset by +1:
dat <- scan(f, quiet = TRUE, what = h, sep = sep, skip = skip +
1, quote = quote, ...)
which means that the first gene is skipped (which then cause problems
because dimensions are not of the same).
Then maPrintTip in marray is confused with how Agilent probes are
positioned and seems to think that there are twice as many probes as
there are. Doing a print tip-based normalization doesn't make much sense
in this case (only 1 print tip is present), but it did end up making the
code crash. This can be fixed by specifying norm='l' (if loess
normalization is wanted) in the agQuality.
I think that should be the default in agQuality and change (in
agQuality):
defs <- list(norm = "p")
to
defs <- list(norm = "l")
As a note, the diagnostic spatial images being produced are not correct
either. It produces 4 copies of the image rather than a single one. I've
attached a the output from a truly horrible array we have where it's
obvious. I assume this is again due to the awkward way Agilent has to
place its spots.
> sessionInfo()
R version 2.2.0, 2005-10-06, x86_64-redhat-linux-gnu
attached base packages:
[1] "grid" "tools" "methods" "stats" "graphics"
"grDevices"
[7] "utils" "datasets" "base"
other attached packages:
arrayQuality RColorBrewer gridBase hexbin colorspace
convert
"1.6.2" "0.2-3" "0.4-1" "1.4.0" "0.9"
"1.4.0"
Biobase marray limma
"1.8.0" "1.8.0" "2.3.7"
Francois
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