Nothing
oneseg <-
function(x, alpha, nperm, sbdry) {
# setup data and parameters for fortran code
data.type <- "logratio"
current.genomdat <- x - mean(x)
current.tss <- sum(current.genomdat^2)
n <- current.n <- length(x)
sbn <- length(sbdry)
# there are used only by hybrid code but need to set it
kmax <- 25
nmin <- 200
ngrid <- 100
tol <- 1e-6
if (n>200) {
hybrid <- TRUE
delta<-(kmax+1)/current.n
} else {
hybrid <- FALSE
delta <- 0
}
# call the fortran segmentation cose
zzz <- .Fortran("fndcpt",
n = as.integer(current.n),
x = as.double(current.genomdat),
tss = as.double(current.tss),
px = double(current.n),
sx = double(n),
nperm = as.integer(nperm),
cpval = as.double(alpha),
ncpt = integer(1),
icpt = integer(2),
ibin = as.logical(data.type=="binary"),
hybrid = as.logical(hybrid),
al0 = as.integer(2),
hk = as.integer(kmax),
delta = as.double(delta),
ngrid = as.integer(ngrid),
sbn = as.integer(sbn),
sbdry = as.integer(sbdry),
tol = as.double(tol),
PACKAGE = "DNAcopy")
# number of changes detected at alpha level (could be 0, 1 or 2)
switch(1+zzz$ncpt, c(zzz$ncpt, 0, 0),
c(zzz$ncpt, 1, zzz$icpt[1]),
c(zzz$ncpt, c(1,0)+zzz$icpt))
}
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