read.snps.long <-function(files, sample.id=NULL, snp.id=NULL, diploid=NULL,
fields=c(sample=1, snp=2, genotype=3, confidence=4),
codes=c("0", "1", "2"), threshold=0.9, lower=TRUE,
sep=" ", comment="#", skip=0,
simplify=c(FALSE, FALSE),
verbose=FALSE, in.order=TRUE, every=1000) {
if (any(duplicated(files)))
stop("duplicated input file name(s)")
if (any(duplicated(sample.id)))
stop("duplicated target sample identifier(s)")
if (any(duplicated(snp.id)))
stop("duplicated target SNP identifier(s)")
if (!is.null(diploid) && any(is.na(diploid)))
stop("diploid argument contains one or more NA's")
if (length(diploid)==1)
diploid <- rep(diploid, length(sample.id))
if (!is.integer(fields))
mode(fields) <- "integer"
.Call("insnp_new", files, sample.id, snp.id, diploid, fields,
codes, threshold, lower, sep, comment, as.integer(skip),
simplify, verbose, in.order, as.integer(every), PACKAGE="snpStats")
}
read.mach <- function(file, colnames=NULL, nrow=NULL) {
.Call("read_mach", file, colnames, nrow, PACKAGE="snpStats")
}
read.impute <- function(file, rownames=NULL, nsnp=NULL, snpcol=2) {
.Call("read_impute", file, rownames, nsnp, snpcol, FALSE, PACKAGE="snpStats")
}
read.beagle <- function(file, rownames=NULL, nsnp=NULL, header=TRUE) {
.Call("read_impute", file, rownames, nsnp, 0, header, PACKAGE="snpStats")
}
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