#' Internal wateRmelon functions for calculating betas
#'
#' db1 is used for quantile normalizing methylated together with unmethylated
#' (dye bias methods nanet, nanes, danes and danet. dfs* functions are used
#' for smoothing the background equalization in methods whose names start with
#' d (daten etc).
#'
#' db1 - quantile normalizes methylated against unmethylated (basic function
#' for dyebuy* dye bias methods). dfsfit - corrects the difference in
#' backgrounds between type I and type II assays and fits a linear model to
#' Sentrix rows and columns if these are available to improve precision where
#' there is a background gradient. dfs2 - finds the difference between type I
#' and type II assay backgrounds for one or more samples. %% ~~ If necessary,
#' more details than the description above ~~
#'
#' @aliases db1 dfs2 dfsfit
#' @param mn,x matrix of methylated signal intensities, each column
#' representing a sample (default method), or an object for which a method is
#' available. For dfsfit and dfs2 this can also be a matrix of unmethylated
#' intensities.
#' @param un matrix of unmethylated signal intensities, each column
#' representing a sample (default method) or NULL when mn is an object
#' containing methylated and unmethylated values.
#' @param onetwo character vector or factor of length nrow(mn) indicating assay
#' type 'I' or 'II'
#' @param roco roco for dfsfit giving Sentrix rows and columns. This allows a
#' background gradient model to be fit. This is split from data column names
#' by default. roco=NULL disables model fitting (and speeds up processing),
#' otherwise roco can be supplied as a character vector of strings like
#' 'R01C01' (3rd and 6th characters used).
#' @return{ \item{name db1}{description a list of 2 matrices of intensities, methylated and
#' unmethylated} \item{nmae dfsfit}{description a matrix of adjusted intensities} \item{name dfs2}{description a background
#' offset value}
#' }
#' @author Leo Schalkwyk <lschal@@essex.ac.uk>
#' @references Pidsley R, Wong CCY, Volta M, Lunnon K, Mill J, Schalkwyk LC: A
#' data-driven approach to preprocessing Illumina 450K methylation array data
#' (submitted)
#' @export db1
db1 <-
function(mn, un ){
stopifnot(dim(un) == dim(mn))
a <- dim(un)[2]
mun <- normalizeQuantiles(cbind(mn,un))
mnn <- mun[,1:a]
unn <- mun[,(a+1):(2*a)]
list(mnn,unn)
}
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