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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