[BioC] mergeScans function in limma - minFactor error
Agnieszka Żmieńko
akisiel at ibch.poznan.pl
Thu Jan 26 10:34:33 CET 2012
Hello everyone.
I am using limma for microarray analysis for some time. Now I am trying
to use mergeScans function to merge scans made with different laser
intensities. Each time I get the same error. I have tried to google-out
the solution but I do not much understand the discussions I've found. As
I am just a biologist and my R activity is mostly modifying commands
that I have found in the manuals or web., my question is - is there any
simple way to deal with it, without large programming skills and
knowledge (plese explain what kind of error is that, is it something
wrong with my data, what can I do) or do I need to find someone who
knows R better than me to help me overcome it?
Thank you
Agnieszka
This is one of my trials - Agilent two-color arrays, scanned and
analyzed in GenePix:
> RG1=read.maimages(targets1, source="genepix.custom",
other.columns=c("ControlType"), wt.fun = wtflags(weight=0, cutoff=-50))
Custom background: MorphologicalOpening
Read 252162310143_1_of_0004_sat1_0635.gpr
> RG2=read.maimages(targets2, source="genepix.custom",
other.columns=c("ControlType"), wt.fun = wtflags(weight=0, cutoff=-50))
Custom background: MorphologicalOpening
Read 252162310143_1_of_0004_0635.gpr
>
> RG1 <- mergeScansRG(RG2,RG1)
Error in nls(y ~ .hockey(x = x, alpha1, beta1, beta2, brk), start =
list(alpha1 = alpha1, :
step factor 0.000488281 reduced below 'minFactor' of 0.000976563
.pl
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