Description Usage Arguments Details Value Author(s) Examples
Plot stacked overview for genome with or without cytobands. It's a
wrapper around layout_karyogram
.
1 2 3 4 5 6 |
obj |
a |
... |
arguments passed to graphic functions to control aesthetics. For
example, if you use geom "point", you need to provide "y" in
|
xlab |
label for x |
ylab |
label for y |
main |
title for plot. |
geom |
geom plotted on the stacked layout. Default is "rect", which showing
interval data as rectangles. It automatically figures out boundary
so you don't have to provide information in |
cytobands |
logical value. Default is |
rescale |
logical value. Default is |
rescale.range |
Numeric range of length 2. Default is (0, 10), because stacked layout draws a white background as chromosome space and this space is of height 10. We hide the y-axis since we don't need it for stacked overview. Sometime users may want to leave some margin for their data, they can use this arguments to control the rescale. |
Stacked overview is just a arbitrary layout for karyogram
layout, it use facets seqnaems ~ . as default to stack the genome. For
accurate mapping, you need to provide seqlengths
information in
your GRanges
object. Otherwise, data space will be computed for
stacked overview chromosome background, this is _NOT_ the actual
chromosome space!.
A ggplot
object.
Tengfei Yin
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 | ## Not run:
library(biovizBase)
data(hg19IdeogramCyto, package = "biovizBase")
library(GenomicRanges)
## you can also get ideogram by biovizBase::getIdeogram
## make shorter and clean labels
old.chrs <- seqnames(seqinfo(hg19IdeogramCyto))
new.chrs <- gsub("chr", "", old.chrs)
## lst <- as.list(new.chrs)
names(new.chrs) <- old.chrs
new.ideo <- renameSeqlevels(hg19IdeogramCyto, new.chrs)
new.ideo <- keepSeqlevels(new.ideo, c(as.character(1:22) , "X", "Y"))
new.ideo
## sample data
data(darned_hg19_subset500, package = "biovizBase")
idx <- is.na(values(darned_hg19_subset500)$exReg)
values(darned_hg19_subset500)$exReg[idx] <- "unknown"
## you need to add seqlengths for accruate mapping
chrnames <- unique(as.character(seqnames(darned_hg19_subset500)))
data(hg19Ideogram, package = "biovizBase")
seqlengths(darned_hg19_subset500) <- seqlengths(hg19Ideogram)[sort(chrnames)]
dn <- darned_hg19_subset500
values(dn)$score <- rnorm(length(dn))
## plotStackedOverview is a simple wrapper around this functions to
create a stacked layout
plotStackedOverview(new.ideo, cytobands = TRUE)
plotStackedOverview(dn)
plotStackedOverview(dn, aes(color = exReg, fill = exReg))
## this will did the trick for you to rescale the space
plotStackedOverview(dn, aes(x = midpoint, y = score), geom = "line")
plotStackedOverview(dn, aes(x = midpoint, y = score), geom = "line", rescale.range = c(4, 6))
## no rescale
plotStackedOverview(dn, aes(x = midpoint, y = score), geom = "line", rescale = FALSE,
xlab = "xlab", ylab = "ylab", main = "main") + ylab("ylab")
## no object? will ask you for species and query the data on the fly
plotStackedOverview()
plotStackedOverview(cytobands = TRUE)
## End(Not run)
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.