Usage
CopyNumScanParams(cnvar = "Log R Ratio", bafvar = "B Allele Freq", gtvar = c("Allele1 - AB", "Allele2 - AB"), index_genome = integer(), select = integer(), scale = 1000, row.names = 1L)
"show"(object)
Arguments
cnvar
length-one character vector providing name of variable for log R ratios
bafvar
length-one character vector providing name of variable for B allele frequencies
gtvar
length-one character vector providing name of variable for genotype calls
index_genome
integer vector indicating which rows of the of
the source files (e.g., GenomeStudio) to keep. By matching on a sorted GRanges
object containing the feature annotation (see example), the
information on the markers will also be sorted.
select
integer vector specifying indicating which columns of the source files to import (see examples)
scale
length-one numeric vector for rescaling the raw data
and coercing to class integer. By default, the low-level data will
be scaled and saved on disk as integers.
row.names
length-one numeric vector indicating which column
the SNP names are in
object
a CopyNumScanParams
object