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savePairs <- function(x, file, param)
# This function saves all counts in 'x' into a set of gzipped files in 'dir', along with
# an index file specifying the identity of each observed chromosome combination corresponding
# to each file. This speeds up any attempt at random access. The idea is to act as a
# convenience function if you have a matrix of counts (or whatever) and you just want to save it.
#
# written by Aaron Lun
# created some time ago
# last modified 18 November 2017
{
if (any(colnames(x) %in% c("anchor.id", "target.id"))) {
stop("colnames 'anchor.*' and 'target.*' should be changed to 'anchor1.*' and 'anchor2.*'")
}
x <- .enforcePairOrder(x)
if (file.exists(file)) {
unlink(file, recursive=TRUE)
}
# Need to reorder so fragments are sorted by chromosome COMBINATION.
if (!.isDNaseC(param)) {
frag.out <- .splitByChr(param$fragments)
all.chrs <- frag.out$chr
full.chrs <- rep(seq_along(all.chrs), frag.out$last-frag.out$first+1L)
achr <- full.chrs[x$anchor1.id]
tchr <- full.chrs[x$anchor2.id]
new.o <- order(achr, tchr, x$anchor1.id, x$anchor2.id)
} else{
# For DNase-C data, the anchor IDs are assumed to be chromosome indices to 'seqlengths'.
all.chrs <- seqlevels(param$fragments)
achr <- x$anchor1.id
tchr <- x$anchor2.id
new.o <- order(achr, tchr)
x$anchor1.id <- x$anchor2.id <- 0L
}
x <- x[new.o,]
# Identifying stretches with the same chromosome pairs.
new.achr <- achr[new.o]
new.tchr <- tchr[new.o]
if (length(new.achr) > 0L) {
is.diff <- c(TRUE, diff(new.achr)!=0L | diff(new.tchr)!=0L)
first.in.combo <- which(is.diff)
last.in.combo <- c(first.in.combo[-1]-1L, length(new.o))
} else {
first.in.combo <- last.in.combo <- integer(0)
}
# Saving results.
.initializeH5(file)
for (ax in unique(new.achr[first.in.combo])) {
.addGroup(file, all.chrs[ax])
}
for (y in seq_along(first.in.combo)) {
current <- first.in.combo[y]:last.in.combo[y]
cur.a <- all.chrs[new.achr[current[1]]]
cur.t <- all.chrs[new.tchr[current[1]]]
.writePairs(x[current,], file, cur.a, cur.t)
}
invisible(NULL)
}
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