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# code by Stephen Turner (with slight modification "p" -> "Fdr" in ylab)
# http://StephenTurner.us/
# http://GettingGeneticsDone.blogspot.com/
# See license at http://gettinggeneticsdone.blogspot.com/p/copyright.html
manhattan <- function(dataframe, colors=c("gray10", "gray50"), ymax="max", limitchromosomes=1:23, suggestiveline=-log10(1e-5), genomewideline=-log10(5e-8), annotate=NULL, ...) {
CHR <- P <- NULL
d=dataframe
if (!("CHR" %in% names(d) & "BP" %in% names(d) & "P" %in% names(d))) stop("Make sure your data frame contains columns CHR, BP, and P")
if (any(limitchromosomes)) d=d[d$CHR %in% limitchromosomes, ]
d=subset(na.omit(d[order(d$CHR, d$BP), ]), (P>0 & P<=1)) # remove na's, sort, and keep only 0<P<=1
d$logp = -log10(d$P)
d$pos=NA
ticks=NULL
lastbase=0
colors <- rep(colors,max(d$CHR))[1:max(d$CHR)]
if (ymax=="max") ymax<-ceiling(max(d$logp))
if (ymax<8) ymax<-8
numchroms=length(unique(d$CHR))
if (numchroms==1) {
d$pos=d$BP
ticks=floor(length(d$pos))/2+1
} else {
for (i in unique(d$CHR)) {
if (i==1) {
d[d$CHR==i, ]$pos=d[d$CHR==i, ]$BP
} else {
lastbase=lastbase+tail(subset(d,CHR==i-1)$BP, 1)
d[d$CHR==i, ]$pos=d[d$CHR==i, ]$BP+lastbase
}
ticks=c(ticks, d[d$CHR==i, ]$pos[floor(length(d[d$CHR==i, ]$pos)/2)+1])
}
}
if (numchroms==1) {
with(d, plot(pos, logp, ylim=c(0,ymax), ylab=expression(-log[10](italic(Fdr))), xlab=paste("Chromosome",unique(d$CHR),"position"), ...))
} else {
with(d, plot(pos, logp, ylim=c(0,ymax), ylab=expression(-log[10](italic(Fdr))), xlab="Chromosome", xaxt="n", type="n", ...))
axis(1, at=ticks, labels=unique(d$CHR), ...)
icol=1
for (i in unique(d$CHR)) {
with(d[d$CHR==i, ],points(pos, logp, col=colors[icol], ...))
icol=icol+1
}
}
if (!is.null(annotate)) {
d.annotate=d[which(d$SNP %in% annotate), ]
with(d.annotate, points(pos, logp, col="green3", ...))
}
if (suggestiveline) abline(h=suggestiveline, col="blue")
if (genomewideline) abline(h=genomewideline, col="red")
}
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