| doCRMAv1 | R Documentation | 
Estimation and assessment of raw copy numbers at the single locus level (CRMA v1) based on [1]. The algorithm is processed in bounded memory, meaning virtually any number of arrays can be analyzed on also very limited computer systems.
  ## S3 method for class 'AffymetrixCelSet'
doCRMAv1(csR, shift=+300, combineAlleles=TRUE, lengthRange=NULL, arrays=NULL, drop=TRUE,
  verbose=FALSE, ...)
  ## Default S3 method:
doCRMAv1(dataSet, ..., verbose=FALSE)
  ## Default S3 method:
doASCRMAv1(...)
csR, dataSet | 
 An   | 
shift | 
 An tuning parameter specifying how much to shift the probe signals before probe summarization.  | 
combineAlleles | 
 A   | 
lengthRange | 
 An optional   | 
arrays | 
 A   | 
drop | 
 If   | 
verbose | 
 See   | 
... | 
 Additional arguments used to set up   | 
Returns a named list, iff drop == FALSE, otherwise
only ChipEffectSet object.
If you wish to obtain allele-specific estimates for SNPs, which
are needed to call genotypes or infer parent-specific copy numbers,
then use argument combineAlleles=FALSE.  Total copy number
signals are still available.
If you know for certain that you will not use allele-specific
estimates, you will get slightly less noisy signals
(very small difference) if you use combineAlleles=TRUE.
doASCRMAv1(...) is a wrapper for
doCRMAv1(..., combineAlleles=FALSE).
Henrik Bengtsson
[1] H. Bengtsson, R. Irizarry, B. Carvalho & T.P. Speed.
Estimation and assessment of raw copy numbers at the
single locus level,
Bioinformatics, 2008.
For CRMA v2 (recommended by authors), which is a single-array
improvement over CRMA v1, see doCRMAv2().
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