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# Function Name: plotCoverage
# Description: plot genomic coverage across the entire GRanges
# Input: GenomicRanges object with bin counts
# Output: plot
#
# Author: Yue Li
###############################################################################
plotCoverage <- function(x, plotLegend=FALSE, legend.cex=1, ...)
{
stopifnot(!missing(x))
plot(start(x), values(x)$count, type = "s", col = "blue", ...)
if(plotLegend) {
chrname <- as.character(runValue(seqnames(x)))
chrlen <- seqlengths(x)[chrname]
# hack legend to ignore extra arguments
formals(legend) <- c(formals(legend), alist(... = ))
legend("topleft", legend=sprintf("%s:1-%d", chrname, chrlen), cex=legend.cex, ...)
}
}
plotStrandedCoverage <- function(gr, binSize=1000, plotLegend=FALSE, ylim, ...)
{
stopifnot(!missing(gr))
gr.posv <- gr[strand(gr) == '+', ]
gr.negv <- gr[strand(gr) == '-', ]
xpos <- binCount(gr.posv, binSize)
xneg <- binCount(gr.negv, binSize)
posCount <- values(xpos)$count
negCount <- values(xneg)$count
if(missing(ylim)) ylim <- min(max(posCount), max(negCount)) * c(-1, 1)
plotCoverage(x=xpos, ylim = ylim, plotLegend=plotLegend, ...)
lines(start(xneg), -negCount, type = "s", col = "red")
abline(h = 0, col = "dimgray")
}
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