Nothing
library(genoCN)
setwd("~/research/CNV/data/HapMap/CEU/")
info = read.table("snp_info_hg18.txt", header=TRUE, sep="\t", as.is=TRUE)
dat = read.table("NA06993.txt", sep=",", header=TRUE, as.is=TRUE)
dat[1:2,]
info[1:2,]
if(any(! dat$Name %in% info$Name)){
stop("missing SNP information \n")
}
mt = match(info$Name, dat$Name)
wNA = which(is.na(mt))
if(length(wNA)>0){
info = info[-wNA,]
mt = mt[-wNA]
}
dat = dat[mt,]
wkp = which(info$Chr %in% as.character(1:22))
dat = dat[wkp,]
info = info[wkp,]
sampleID = dat$Sample[1]
Theta = genoCNV(info$Name, info$Chr, info$Position, dat$LRR, dat$BAF,
info$PFB, sampleID, cnv.only=(info$PFB>1), outputSeg = TRUE,
outputSNP = 1, outputTag = sampleID)
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