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### =========================================================================
### bedtools multiinter command
### -------------------------------------------------------------------------
###
bedtools_multiinter <- function(cmd = "--help") {
do_R_call(R_bedtools_multiinter, BEDTOOLS_MULTIINTER_DOC, cmd)
}
.R_bedtools_disjoin <- function(i, header=FALSE, names=NULL,
g=NA_character_, empty=FALSE, use.score=FALSE)
{
stopifnot((is.character(i) && !anyNA(i) && length(i) >= 1L) || hasRanges(i),
isTRUEorFALSE(header),
isGenome(g),
isTRUEorFALSE(empty),
isTRUEorFALSE(use.score))
if (!is.null(names)) {
stopifnot(is.character(names), !anyNA(names),
length(names) == length(i))
}
importGenome(g)
i <- normB(i)
if (use.score) {
.gr_i <- importB(i, names)
} else {
.gr_i <- importB(i, names, beforeStack=reduce)
}
.gr_i_o <- prepOverlapRanges(i)
R(dj <- disjoin(.gr_i, ignore.strand=TRUE, with.revmap=TRUE))
rm(i)
if (use.score) {
R(mcols(.gr_i)$i <- decode(mcols(.gr_i)$i))
R(dfl <- extractList(mcols(.gr_i), mcols(dj)$revmap))
R(assay <- as.matrix(dfl[,"score"], col.names=dfl[,"i"]))
R(rowData <- granges(dj))
} else {
R(mcols(dj)$i <- extractList(decode(mcols(.gr_i)$i), mcols(dj)$revmap))
}
if (empty) {
R(none <- setdiff(as(seqinfo(dj), "GRanges"), dj))
if (use.score) {
R(assay <- rbind(assay,
matrix(nrow=length(none), ncol=ncol(assay))))
R(rowData <- c(rowData, none))
} else {
R(mcols(none)$revmap <- IntegerList(integer()))
R(mcols(none)$i <- FactorList(factor()))
R(dj <- sort(c(dj, none)))
}
}
if (use.score) {
R(ans <- SummarizedExperiment(list(score=assay), rowData))
if (empty) {
R(ans <- sort(ans))
}
} else {
R(ans <- dj)
}
R(ans)
}
R_bedtools_multiinter <- function(i, header=FALSE, names=NULL,
g=NA_character_, empty=FALSE)
{
.R_bedtools_disjoin(i, header, names, g, empty)
}
BEDTOOLS_MULTIINTER_DOC <-
"Usage:
bedtools_multiinter [options]
Options:
-i <FILE,...> BAM/BED/GFF/VCF files.
-header Print a header line. (chrom/start/end + names of each file).
--names <name,...> A list of names to describe each file in -i.
These names will be printed in the header line.
-g <id> Use genome file to calculate empty regions.
--empty Report empty regions (i.e., start/end intervals w/o
values in all files)."
do_bedtools_multiinter <- make_do(R_bedtools_multiinter)
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