Usage
AnalyzeTilingCelFiles(CEL_filenames, BPMAP_filename, outfilename=NULL, iID=NULL, iCHR=NULL, iSTART=NULL, iEND=NULL, makeUniqueID=TRUE, readOnlyNCBI=TRUE, readProbeSeq=FALSE, IgnoreBpmapCelPlatformMismatch=FALSE, ReturnRawIntensities=FALSE)
Arguments
CEL_filenames
A character vector of the path to all CEL file(s) in the analysis.
BPMAP_filename
The path to the BPMAP file which describes the arrays specified in the cel files.
outfilename
If specified, the function writes a tab-separated table of normalized intensities.
iID
Vector of IDs for each interval specified.
iCHR
Vector of chromosomes for each interval.
iSTART
Integer vector of the interval start.
iEND
Integer vector of the interval end.
makeUniqueID
If TRUE (default), returns a column of unique identifiers for each probe, of the form: chr-start.
readOnlyNCBI
If TRUE (default), returns ONLY probes that target NCBI sequences, TIGR and Affymetrix controls are ignored.
readProbeSeq
If TRUE, returns the first 25 bp of the probe sequence.
IgnoreBpmapCelPlatformMismatch
If TRUE, ignores a mismatch between BPMAP and CEL platforms. (EXPERT ONLY!)
ReturnRawIntensities
If TRUE, returns raw intensity values associated with the specified regions. Otherwise (default) preforms RMA-like processing of data using the affy package. Processing includes background correction, quantile normalization, and a log-2 transform.