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######################################################################
#
# est.rf.R
#
# copyright (c) 2001-2017, Karl W Broman
# last modified Sep, 2017
# first written Apr, 2001
#
# This program is free software; you can redistribute it and/or
# modify it under the terms of the GNU General Public License,
# version 3, as published by the Free Software Foundation.
#
# This program is distributed in the hope that it will be useful,
# but without any warranty; without even the implied warranty of
# merchantability or fitness for a particular purpose. See the GNU
# General Public License, version 3, for more details.
#
# A copy of the GNU General Public License, version 3, is available
# at http://www.r-project.org/Licenses/GPL-3
#
# Part of the R/qtl package
# Contains: est.rf, plotRF, checkAlleles, pull.rf, plot.rfmatrix
#
######################################################################
######################################################################
#
# est.rf: Estimate sex-averaged recombination fractions between
# all pairs of markers
#
######################################################################
est.rf <-
function(cross, maxit=10000, tol=1e-6)
{
if(!any(class(cross) == "cross"))
stop("Input should have class \"cross\".")
n.chr <- nchr(cross)
n.mar <- totmar(cross)
n.ind <- nind(cross)
mar.names <- unlist(lapply(cross$geno,function(a) colnames(a$data)))
type <- class(cross)[1]
chrtype <- sapply(cross$geno,class)
is.bcsft <- (type == "bcsft")
if(is.bcsft) {
cross.scheme <- attr(cross, "scheme") ## c(s,t) for BC(s)F(t)
is.bcsft <- cross.scheme[2] > 0 ## used for fixX only
}
xchrcol <- NULL
fixX <- FALSE
Geno <- NULL
# create full genotype matrix
for(i in 1:n.chr) {
temp <- cross$geno[[i]]$data
# treat X chromosome specially in an intercross or BCsFt with t>0.
if((type=="f2" || is.bcsft) && chrtype[i]=="X") {
fixX <- TRUE
if(i != 1) xchrcol <- c(xchrcol,ncol(Geno)+(1:ncol(cross$geno[[i]]$data)))
else xchrcol <- 1:ncol(cross$geno[[i]]$data)
xchr <- temp
xchr[is.na(xchr)] <- 0
temp <- reviseXdata("f2","simple",getsex(cross),geno=temp,
cross.attr=attributes(cross))
}
Geno <- cbind(Geno,temp)
}
# which type of cross is this?
if(type == "f2")
cfunc <- "est_rf_f2"
else if(type == "bc" || type=="risib" || type=="riself" || type=="dh" || type=="haploid")
cfunc <- "est_rf_bc"
else if(type == "4way")
cfunc <- "est_rf_4way"
else if(type=="ri8sib" || type=="ri8self" || type=="ri4sib" || type=="ri4self") {
cfunc <- paste("est_rf_", type, sep="")
if(any(chrtype == "X"))
warning("est.rf not working properly for the X chromosome for 4- or 8-way RIL.")
}
else if(type == "bcsft")
cfunc <- "est_rf_bcsft"
else
stop("est.rf not available for cross type ", type, ".")
Geno[is.na(Geno)] <- 0
if(type=="bc" || type=="risib" || type=="riself" || type=="dh" || type=="haploid")
z <- .C(cfunc,
as.integer(n.ind), # number of individuals
as.integer(n.mar), # number of markers
as.integer(Geno),
rf = as.double(rep(0,n.mar*n.mar)),
PACKAGE="qtl")
else {
## Hide cross scheme in genoprob to pass to routine. BY
temp <- as.double(rep(0,n.mar*n.mar))
if(type == "bcsft")
temp[1:2] <- cross.scheme
z <- .C(cfunc,
as.integer(n.ind), # number of individuals
as.integer(n.mar), # number of markers
as.integer(Geno),
rf = as.double(temp),
as.integer(maxit),
as.double(tol),
PACKAGE="qtl")
}
cross$rf <- matrix(z$rf,ncol=n.mar)
dimnames(cross$rf) <- list(mar.names,mar.names)
if(fixX) {
temp <- as.double(rep(0, ncol(xchr) ^ 2))
if(type == "bcsft") {
temp[1] <- cross.scheme[1] + cross.scheme[2] - (cross.scheme[1] == 0)
zz <- .C(cfunc,
as.integer(n.ind), # number of individuals
as.integer(ncol(xchr)), # number of markers on X chr.
as.integer(xchr),
rf = as.double(temp),
as.integer(maxit),
as.double(tol),
PACKAGE="qtl")
}
else {
zz <- .C("est_rf_bc",
as.integer(n.ind),
as.integer(ncol(xchr)),
as.integer(xchr),
rf=as.double(temp),
PACKAGE="qtl")
}
zz <- matrix(zz$rf,ncol=ncol(xchr))
cross$rf[xchrcol,xchrcol] <- zz
}
# check for alleles switches
if(type == "risib" || type=="riself" || type=="f2" || type=="bc" || type=="dh" || type=="haploid") {
out <- checkAlleles(cross, 5, FALSE)
if(!is.null(out)) {
out <- as.character(out[,1])
warning("Alleles potentially switched at markers \n ",
paste(out, collapse=" "))
}
}
cross
}
plotRF <-
function(x, chr, what=c("both","lod","rf"),
alternate.chrid=FALSE, zmax=12,
mark.diagonal=FALSE,
col.scheme=c("viridis", "redblue"),
...)
{
if(!any(class(x) == "cross"))
stop("Input should have class \"cross\".")
what <- match.arg(what)
if("onlylod" %in% names(attributes(x$rf)) && attr(x$rf, "onlylod")) {
onlylod <- TRUE
what <- "lod"
}
else onlylod <- FALSE
if(!missing(chr)) x <- subset(x,chr=chr)
if(!("rf" %in% names(x))) {
warning("Running est.rf.")
x <- est.rf(x)
}
g <- x$rf
old.xpd <- par("xpd")
old.las <- par("las")
par(xpd=TRUE,las=1)
on.exit(par(xpd=old.xpd,las=old.las))
if(!onlylod) {
# if any of the rf's are NA (ie no data), put NAs in corresponding LODs
if(any(is.na(g))) g[is.na(t(g))] <- NA
# convert rf to -2*(log2(rf)+1); place zmax's on the diagonal;
# anything above zmax replaced by zmax;
# NA's replaced by -1
g[row(g) > col(g) & g > 0.5] <- 0.5
g[row(g) > col(g)] <- -4*(log2(g[row(g) > col(g)])+1)/12*zmax
}
diag(g) <- zmax
g[!is.na(g) & g>zmax] <- zmax
g[is.na(g)] <- -1
if(what=="lod" && !onlylod) { # plot LOD scores
# copy upper triangle (LODs) to lower triangle (rec fracs)
g[row(g) > col(g)] <- t(g)[row(g) > col(g)]
}
else if(what=="rf") { # plot recombination fractions
# copy lower triangle (rec fracs) to upper triangle (LODs)
g[row(g) < col(g)] <- t(g)[row(g) < col(g)]
}
br <- c(-1, seq(-1e-6, zmax, length=257))
col.scheme <- match.arg(col.scheme)
if(col.scheme=="redblue") {
# convert colors using gamma=0.6 (which will no longer be available in R)
thecol <- rev(rainbow(256, start=0, end=2/3))
rgbval <- (col2rgb(thecol)/255)^0.6
thecol <- rgb(rgbval[1,], rgbval[2,], rgbval[3,])
} else {
thecol <- viridis_qtl(256) # the new default
}
image(1:ncol(g),1:nrow(g),t(g),ylab="Markers",xlab="Markers",breaks=br,
col=c("lightgray",thecol))
if(mark.diagonal) {
for(i in 1:ncol(g))
segments(i+c(-0.5, -0.5, -0.5, +0.5), i+c(-0.5, +0.5, -0.5, -0.5),
i+c(-0.5, +0.5, +0.5, +0.5), i+c(+0.5, +0.5, -0.5, +0.5))
}
# plot lines at the chromosome boundaries
n.mar <- nmar(x)
n.chr <- nchr(x)
a <- c(0.5,cumsum(n.mar)+0.5)
abline(v=a,xpd=FALSE,col="white")
abline(h=a,xpd=FALSE,col="white")
# this line adds a line above the image
# (the image function leaves it out)
abline(h=0.5+c(0,nrow(g)),xpd=FALSE)
abline(v=0.5+c(0,nrow(g)),xpd=FALSE)
# add chromosome numbers
a <- par("usr")
wh <- cumsum(c(0.5,n.mar))
chrnam <- names(x$geno)
chrpos <- (wh[-1] + wh[-length(wh)])/2
if(!alternate.chrid || length(chrnam) < 2) {
for(i in seq(along=chrpos)) {
axis(side=3, at=chrpos[i], labels=chrnam[i], tick=FALSE, line=-0.8)
axis(side=4, at=chrpos[i], labels=chrnam[i], tick=FALSE, line=-0.8)
}
}
else {
odd <- seq(1, length(chrpos), by=2)
even <- seq(2, length(chrpos), by=2)
for(i in odd) {
axis(side=3, at=chrpos[i], labels=chrnam[i], line=-0.8, tick=FALSE)
axis(side=4, at=chrpos[i], labels=chrnam[i], line=-0.8, tick=FALSE)
}
for(i in even) {
axis(side=3, at=chrpos[i], labels=chrnam[i], line=0, tick=FALSE)
axis(side=4, at=chrpos[i], labels=chrnam[i], line=0, tick=FALSE)
}
}
dots <- list(...)
if("main" %in% names(dots))
title(main=dots$main)
else {
if(what=="lod") title(main="Pairwise LOD scores")
else if(what=="rf") title(main="Recombination fractions")
else title("Pairwise recombination fractions and LOD scores")
}
invisible()
}
######################################################################
# check for apparent errors in the recombination fractions
######################################################################
#checkrf <-
#function(cross, threshold=5)
#{
# rf <- cross$rf
# n.mar <- nmar(cross)
# map <- pull.map(cross)
# n <- ncol(rf)
# mnam <- colnames(rf)
# whpos <- unlist(lapply(map,function(a) 1:length(a)))
# whchr <- rep(names(map),sapply(map,length))
#
# # first check whether a locus has "significant" pairwise recombination
# # with rf > 0.5
# for(i in 1:n) {
# if(i == 1) {
# lod <- rf[1,-1]
# r <- rf[-1,1]
# }
# else if(i == n) {
# lod <- rf[-n,n]
# r <- rf[n,-n]
# }
# else {
# lod <- c(rf[1:(i-1),i],rf[i,(i+1):n])
# r <- c(rf[i,1:(i-1)],rf[(i+1):n,i])
# }
#
# # if rf > 1/2 and LOD > threshold for more than two other markers
# if(sum(!is.na(lod) & !is.na(r) & lod > threshold & r > 0.5) >= 2)
# warning("Genotypes potentially switched for marker ", mnam[i],
# paste(" (",whpos[i],")",sep=""), " on chr ", whchr[i], "\n")
#
# }
#
#}
######################################################################
# checkAlleles()
#
# Function to find markers that may have alleles miscoded;
# we go through each marker, one at a time, swap alleles and
# then see what it does to pairwise linkage against all other
# markers
######################################################################
checkAlleles <-
function(cross, threshold=3, verbose=TRUE)
{
if(!any(class(cross) == "cross"))
stop("checkAlleles() only works for cross objects.")
type <- class(cross)[1]
if(type != "f2" && type != "bc" &&
type != "risib" && type != "riself" && type != "dh" && type!="haploid")
stop("checkAlleles not available for cross type ", type, ".")
# drop X chromosome
chrtype <- sapply(cross$geno,class)
if(all(chrtype=="X")) {
if(verbose) cat("checkAlleles() only works for autosomal data.\n")
return(NULL)
}
cross <- subset(cross, chr = (chrtype != "X"))
n.mar <- nmar(cross)
mar.names <- unlist(lapply(cross$geno,function(a) colnames(a$data)))
if(!("rf" %in% names(cross))) {
warning("First running est.rf.")
cross <- est.rf(cross)
}
diag(cross$rf) <- 0
lod <- rf <- cross$rf
lod[lower.tri(lod)] <- t(lod)[lower.tri(lod)]
rf[upper.tri(rf)] <- t(rf)[upper.tri(rf)]
orig.lod <- rev.lod <- lod
orig.lod[rf > 0.5] <- 0
rev.lod[rf < 0.5] <- 0
dif <- apply(rev.lod, 2, max, na.rm=TRUE) -
apply(orig.lod, 2, max, na.rm=TRUE)
results <- data.frame(marker=mar.names,
chr=rep(names(cross$geno), n.mar),
index=unlist(lapply(n.mar, function(a) 1:a)),
"diff in max LOD" = dif, stringsAsFactors=TRUE)
rownames(results) <- 1:nrow(results)
if(all(results[,4] < threshold)) {
if(verbose) cat("No apparent problems.\n")
return(invisible(NULL))
}
results[results[,4] >= threshold,]
}
######################################################################
# pull.rf
#
# pull out the pairwise marker recombination fraction estimates,
# with class "rfmatrix"
######################################################################
pull.rf <-
function(cross, what=c("rf", "lod"), chr)
{
if(!("cross" %in% class(cross)))
stop("Input must have class \"cross\".")
if(!missing(chr)) cross <- subset(cross, chr=chr)
if(!("rf" %in% names(cross))) {
warning(" -Running est.rf")
cross <- est.rf(cross)
}
rf <- cross$rf
if(nrow(rf) != totmar(cross) || ncol(rf) != totmar(cross) ||
any(rownames(rf) != markernames(cross)) ||
any(colnames(rf) != markernames(cross))) {
warning(" -Rec. frac. estimates seem corrupted; re-running est.rf")
cross <- est.rf(cross)
}
rf <- cross$rf
diag(rf) <- NA
what <- match.arg(what)
if(what=="rf")
rf[upper.tri(rf)] <- t(rf)[upper.tri(rf)]
else
rf[lower.tri(rf)] <- t(rf)[lower.tri(rf)]
attr(rf, "map") <- pull.map(cross, as.table=TRUE)
attr(rf, "what") <- what
class(rf) <- c("rfmatrix", "matrix")
rf
}
######################################################################
# plot.rfmatrix:
#
# plot a slice through the matrix (that is, for one marker)
######################################################################
plot.rfmatrix <-
function(x, marker, ...)
{
if(!("rfmatrix" %in% class(x)))
stop("Input must have class \"rfmatrix\".")
if(missing(marker))
stop("You must provide a marker name.")
if(length(marker) > 1) {
warning("Ignoring all but the first marker, ", marker[1])
marker <- marker[1]
}
if(!(marker %in% rownames(x)))
stop("Marker ", marker, " not found.")
what <- attr(x, "what")
x <- cbind(attr(x, "map"), x[marker,])
x$chr <- factor(x$chr, levels=unique(x$chr))
# fill in hole
wh <- which(rownames(x)==marker)
if(wh > 1 && wh < nrow(x) && x[wh-1,1] == x[wh,1] && x[wh+1,1] == x[wh,1]) {
xl <- x[wh-1,2]
xm <- x[wh,2]
xr <- x[wh+1,2]
yl <- x[wh-1,3]
yr <- x[wh+1,3]
x[wh,3] <- yl + (xm-xl)*(yr-yl)/(xr-xl)
}
colnames(x)[3] <- what
class(x) <- c("scanone", "data.frame")
dots <- list(...)
if("main" %in% names(dots))
plot(x, ...)
else
plot(x, main=marker, ...)
invisible(x)
}
# end of est.rf.R
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