Nothing
## A srFilter for use with e.g. readAligned()
chipseqFilter <- function(exclude = "[_MXY]",
uniqueness = c("location", "sequence",
"location*sequence", "none"),
hasStrand = TRUE)
{
if (!is.null(exclude) && (!is.character(exclude) || any(is.na(exclude))))
stop("'exclude' must be character without NA's")
uniqueness <- match.arg(uniqueness)
if (!isTRUEorFALSE(hasStrand))
stop("'hasStrand' must be TRUE or FALSE")
filt <- srFilter()
if (hasStrand)
filt <- compose(filt, strandFilter(strandLevels=c("-", "+")))
if (!is.null(exclude))
filt <- compose(filt, chromosomeFilter(exclude, exclude = TRUE))
if (uniqueness != "none") {
withSread <- switch(uniqueness, location = FALSE, sequence = NA,
`location*sequence` = TRUE)
ofilt <-
occurrenceFilter(withSread = withSread)
filt <- compose(filt, ofilt)
}
filt
}
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