circos.genomicDensity | R Documentation |
Calculate and add genomic density track
circos.genomicDensity(
data,
ylim.force = FALSE,
window.size = NULL,
overlap = TRUE,
count_by = c("percent", "number"),
col = ifelse(area, "grey", "black"),
lwd = par("lwd"),
lty = par("lty"),
type = "l",
area = TRUE,
area.baseline = NULL,
baseline = 0,
border = NA,
...)
data |
A bed-file-like data frame or a list of data frames. If the input is a list of data frames. there will be multiple density plot in one same track. |
ylim.force |
Whether to force upper bound of |
window.size |
Pass to |
overlap |
Pass to |
count_by |
Pass to |
col |
Colors. It should be length of one. If |
lwd |
Width of lines, the same setting as |
lty |
Style of lines, the same setting as |
type |
Type of lines, see |
area |
See |
area.baseline |
Deprecated, use |
baseline |
See |
border |
See |
... |
Pass to |
This function is a high-level graphical function, and it will create a new track.
If you have multiple sets of genomic regions, you should make sure the density ranges
for all sets are similar, or I suggest you should put them into different tracks. One example
can be found in the "Examples" Section where the density range for bed_list[[2]]
is too high
compared to the range for bed_list[[1]]
, thus, it is better to put the two sets of
regions into two separate tracks.
load(system.file(package = "circlize", "extdata", "DMR.RData"))
# rainfall
circos.initializeWithIdeogram(plotType = c("axis", "labels"))
bed_list = list(DMR_hyper, DMR_hypo)
circos.genomicRainfall(bed_list, pch = 16, cex = 0.4, col = c("#FF000080", "#0000FF80"))
circos.genomicDensity(bed_list[[1]], col = c("#FF000080"), track.height = 0.1)
circos.genomicDensity(bed_list[[2]], col = c("#0000FF80"), track.height = 0.1)
circos.clear()
############ draw the two densities in one track #############
circos.initializeWithIdeogram(plotType = c("axis", "labels"))
circos.genomicDensity(bed_list, col = c("#FF000080", "#0000FF80"), track.height = 0.2)
circos.clear()
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