"marrayRaw"
from spot quantification data files obtained from image analysis software or databases.
read.marrayRaw(fnames, path=".", name.Gf=NULL, name.Gb=NULL, name.Rf=NULL,
name.Rb=NULL,name.W=NULL, layout=NULL, gnames=NULL, targets=NULL,
notes=NULL, skip=NULL, sep=" ", quote="\"", DEBUG=FALSE, ...)
read.GenePix(fnames = NULL, path = NULL, name.Gf = "F532 Median",
name.Gb ="B532 Median", name.Rf = "F635 Median", name.Rb = "B635 Median",
name.W ="Flags", layout = NULL, gnames = NULL, targets = NULL,
notes = NULL, skip=NULL, sep = " ", quote = "\"", DEBUG=FALSE, ...)
read.SMD(fnames = NULL, path = NULL, name.Gf = "Ch1 Intensity (Median)",
name.Gb = "Ch1 Background (Median)", name.Rf = "Ch2 Intensity (Median)",
name.Rb = "Ch2 Background (Median)", name.W = NULL, info.id = c("Name",
"Clone ID"), layout = NULL, gnames = NULL, targets = NULL, notes = NULL, skip = NULL, sep = "\t", quote = "\"", DEBUG=FALSE, ...)
read.Spot(fnames = NULL, path = ".", name.Gf = "Gmean", name.Gb =
"morphG", name.Rf = "Rmean", name.Rb = "morphR",name.W = NULL, layout =
NULL, gnames = NULL, targets = NULL, notes = NULL, skip = NULL, sep = "\t", quote = "\"", DEBUG=FALSE, ...)
read.Agilent(fnames = NULL, path=NULL, name.Gf = "gMedianSignal", name.Gb = "gBGMedianSignal", name.Rf = "rMedianSignal", name.Rb = "rBGMedianSignal", name.W= NULL, layout = NULL, gnames = NULL, targets = NULL, notes=NULL, skip=NULL, sep="\t", quote="\"", DEBUG=FALSE, info.id=NULL, ...)
widget.marrayRaw(ext = c("spot", "xls", "gpr"), skip = 0, sep = "\t", quote = "\"", ...)
.spot
for the software Spot
or .gpr
for the software GenePix
.fnames
contains the full path name, path should be set
to NULL."marrayLayout"
, containing microarray layout parameters."marrayInfo"
containing probe sequence information."marrayInfo"
containing target sample information."character"
, vector of explanatory
text."character"
, vector containing
the name of the colums of the SMD file containing oligo information
you want to retrieve. By default, this is set to read Homo sapiens
data. You may need to modify this argument if your are working on
another genome.quote="\""
.scan
."marrayRaw"
.
scan
, read.marrayLayout
,
read.marrayInfo
datadir <- system.file("swirldata", package="marray")
## Quick guide
swirl.targets <- read.marrayInfo(file.path(datadir, "SwirlSample.txt"))
data <- read.Spot(path=datadir, targets=swirl.targets)
## Alternate commands
skip <- grep("Row", readLines(file.path(datadir,"fish.gal"), n=100)) - 1
swirl.layout <- read.marrayLayout(ngr=4, ngc=4, nsr=22, nsc=24)
swirl.targets <- read.marrayInfo(file.path(datadir, "SwirlSample.txt"))
swirl.gnames <- read.marrayInfo(file.path(datadir, "fish.gal"),
info.id=4:5, labels=5, skip=skip)
x <- maInfo(swirl.gnames)[,1]
y <- rep(0, maNspots(swirl.layout))
y[x == "control"] <- 1
slot(swirl.layout, "maControls") <- as.factor(y)
fnames <- dir(path=datadir,pattern="spot")
swirl<- read.Spot(fnames, path=datadir,
layout = swirl.layout,
gnames = swirl.gnames,
targets = swirl.targets)
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