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marjan
2013 Jan 29
0
Bioconductor flowcytometry
...g problem.
the code i use now is the following:
logTransi <- truncateTransform("truncate at 1", a=1)
testSetLog <- transform(testSet, 'FL10'= logTransi('FL10'),
'FL11'=logTransi('FL11'))
testSet looks like this:
> testSet
flowFrame object 'MarjanD.20120926.A.0026.fcs'
with 100000 cells and 14 observables:
name desc range minRange maxRange
$P1 pulse.width <NA> 65536 768 65535
$P2 FSC_PER <NA> 65536 0 65535
$P3 FSC_PAR <NA> 65536 0 65535
$P4 SSC <NA> 65536...