plotAB | R Documentation |
Plot A/B compartments bins
plotAB(
x,
chr = NULL,
what = "score",
main = "",
ylim = c(-1, 1),
unitarize = FALSE,
reverse = FALSE,
top.col = "deeppink4",
bot.col = "grey50",
with.ci = FALSE,
filter = TRUE,
filter.min.eigen = 0.02,
median.conf = FALSE
)
x |
The matrix obejct returned from getCompartments |
chr |
Chromosome to subset to for plotting |
what |
Which metadata column to plot |
main |
Title for the plot |
ylim |
Y-axis limits (default is -1 to 1) |
unitarize |
Should the data be unitarized? |
reverse |
Reverse the sign of the PC values? |
top.col |
Top (pos. PC values) chromatin color to be plotted |
bot.col |
Bottom (neg. PC values) chromatin color to be plotted |
with.ci |
Whether to plot confidence intervals |
filter |
Whether to filter eigenvalues close to zero (default: TRUE) |
filter.min.eigen |
Minimum absolute eigenvalue to include in the plot |
median.conf |
Plot the median confidence estimate across the chromosome? |
A plot of inferred A/B compartments
library(GenomicRanges)
#Generate random genomic intervals of 1-1000 bp on chr1-22
#Modified from https://www.biostars.org/p/225520/
random_genomic_int <- data.frame(chr = rep("chr14", 100))
random_genomic_int$start <- apply(random_genomic_int, 1, function(x) { round(runif(1, 0, getSeqLengths(chr = x)[[1]]), 0) })
random_genomic_int$end <- random_genomic_int$start + runif(1, 1, 1000)
random_genomic_int$strand <- "*"
#Generate random counts
counts <- rnbinom(1000, 1.2, 0.4)
#Build random counts for 10 samples
count.mat <- matrix(sample(counts, nrow(random_genomic_int) * 10, replace = FALSE), ncol = 10)
colnames(count.mat) <- paste0("sample_", seq(1:10))
#Bin counts
bin.counts <- getBinMatrix(count.mat, makeGRangesFromDataFrame(random_genomic_int), chr = "chr14", genome = "hg19")
#Calculate correlations
bin.cor.counts <- getCorMatrix(bin.counts)
#Get A/B signal
absignal <- getABSignal(bin.cor.counts)
#Plot the A/B signal
par(mar=c(1,1,1,1))
par(mfrow=c(1,1))
plotAB(absignal, what = "pc")
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