read.rg(files = NULL, source = "generic", path = NULL, ext = NULL, names = NULL, columns = NULL, other.columns = NULL, annotation = NULL,wt.fun = NULL, verbose = TRUE, sep = "\t", quote = NULL, DEBUG = FALSE, ...)ext in the specified directory will be read in
alphabetical order."generic",
"agilent", "arrayvision", "bluefuse", "genepix",
"genepix.custom", "genepix.median", "imagene",
"quantarray", "scanarrayexpress", "smd.old",
"smd", "spot" or "spot.close.open".removeExt(files).R, G, Rb, Gb,
RArea and GArea giving the column names to be used for
red foreground, green foreground, red background, green background,
red area and green area respectively. Or, in the case of Imagene data,
a list with fields f and b. This argument is optional
if source is specified, otherwise it is required.TRUE to report each time a file is read TRUE, a series of echo statements
will be printed for each file. Details on the file, skip,
and selected columns in a colClasses format for read.table
will be displayed.read.table.RGList_CALIB object
containing the componentswt.fun is givenother.columns if givensource is "agilent",
"genepix" or source="imagene" or if the annotation
argument is setFileName giving the names of the
files readPrintLayout, currently set only if
source="imagene"RGList_CALIB object. However,there
are two more fields - $RArea and $GArea than RGList
object in limma package. These two fields contain spot area of each color.
More details see read.maimages in limma package.
read.maimages in limma packageread.table in the base package
# Read all .gpr files from current working directory.
# files <- dir(pattern="*\.gpr$")
# RG <- read.rg(files,"genepix")
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