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#' sideHist
#'
#' Plots two histograms side by side with smoothed density overlay
#'
#'
#' @param x First numeric vector of data to plot.
#'
#' @param y Second numeric vector of data to plot.
#'
#' @param logT Logical that indicates whether to take the log(x+1)
#' transformation.
#'
#' @param title.gene Character vector that contains the gene name that you
#' are plotting
#'
#' @return NULL (creates a baseR plot)
#'
#' @references Korthauer KD, Chu LF, Newton MA, Li Y, Thomson J, Stewart R,
#' Kendziorski C. A statistical approach for identifying differential
#' distributions
#' in single-cell RNA-seq experiments. Genome Biology. 2016 Oct 25;17(1):222.
#' \url{https://genomebiology.biomedcentral.com/articles/10.1186/s13059-016-
#' 1077-y}
sideHist <- function(x, y, logT=TRUE, title.gene=""){
# grab some pretty ggplot colors
ggplotColours <- function(n=6, h=c(0, 360) +15){
if ((diff(h)%%360) < 1) h[2] <- h[2] - 360/n
hcl(h = (seq(h[1], h[2], length = n)), c = 100, l = 65)
}
valsA <- y
valsB <- x
if (logT){
valsA <- log(valsA+1)
valsB <- log(valsB+1)
}
binwidth <- 0.35
bin.points <- seq(range(c(valsA,valsB))[1]-0.5,
range(c(valsA,valsB))[2]+0.5, by=binwidth)
A <- hist(valsA, breaks=bin.points, plot=FALSE)
B <- hist(valsB, breaks=bin.points, plot=FALSE)
gcol <- ggplotColours(2)
densrange <- c(-max(c(B$density, A$density)), max(c(A$density, B$density)))
plot(NULL, type = "n", xlim = densrange,
ylim = c(range(c(A$breaks, B$breaks))), ylab="log(EC + 1)",
xlab="density", xaxt="n",
main = paste0("Gene ", title.gene))
axis(1, at=seq(-2,2,by=0.1), labels=abs(seq(-2,2,by=0.1)))
rect(0, A$breaks[1:(length(A$breaks) - 1)], A$density,
A$breaks[2:length(A$breaks)], col=gcol[1])
rect(0, B$breaks[1:(length(B$breaks) - 1)], -B$density,
B$breaks[2:length(B$breaks)], col=gcol[2])
lines(density(valsA, adjust=1.25)$y,
density(valsA, adjust=1.25)$x, col="darkgrey", lwd=2)
lines(-density(valsB, adjust=1.25)$y,
density(valsB, adjust=1.25)$x, col="darkgrey", lwd=2)
}
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