##' GetIndxPositionFromChips: Unknown.
##'
##' Specifically designed to handle noisy data from amplified DNA on phenylketonuria (PKU) cards. The function is a pipeline using many subfunctions.
##' @title GetIndxPositionFromChips
##' @param CNVs: Data frame with information on CNVs. Unknown.
##' @param Sample: Unknown.
##' @return Data frame with predicted CNVs.
##' @author Marcelo Bertalan, Louise K. Hoeffding.
##' @source \url{http://biopsych.dk/iPsychCNV}
##' @export
##' @examples Unknown.
##'
GetIndxPositionFromChips <- function(CNVs, Sample)
{
Res2 <- sapply(unique(CNVs$Chr), function(y)
{
CHR2 <- y
CHR2 <- gsub(" ", "", CHR2)
df2 <- subset(CNVs, Chr %in% CHR2)
subSample <- subset(Sample, Chr %in% CHR2) # Subset by Chr
subSample <- subSample[with(subSample, order(Position)),]
Res <- sapply(1:nrow(df2), function(i)
{
X <- df2[i,]
StartM <- as.numeric(X["Start"]) # CNV Start
StopM <- as.numeric(X["Stop"])
# Order
StartIndx <- which.min(abs(subSample$Position - StartM))
StopIndx <- which.min(abs(subSample$Position - StopM))
NumSNPs <- StopIndx - StartIndx
StartM <- subSample$Position[StartIndx]
StopM <- subSample$Position[StopIndx]
SNP.Start <- subSample$SNP.Name[StartIndx]
SNP.Stop <- subSample$SNP.Name[StopIndx]
df <- data.frame(Start=StartM, Stop=StopM, Chr=CHR2, StartIndx=StartIndx, StopIndx=StopIndx, NumSNPs=NumSNPs, SNP.Start=SNP.Start, SNP.Stop=SNP.Stop, stringsAsFactors=F)
#df <- data.frame(StartIndx=StartIndx, StopIndx=StopIndx, NumSNPs=NumSNPs)
df3 <- cbind(df, df2[i,])
return(df3)
})
df <- MatrixOrList2df(tmp=Res)
return(df)
})
df <- MatrixOrList2df(tmp=Res2)
return(df)
}
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