gatk-3.8/R/VariantRecalibratorReport/VariantRecalibratorReport.R

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An R module that takes in a Variant Recalibration cluster file (file with '@!CLUSTER' lines in it), a tabularized VCF, and optionally a set of loci that should be examined more carefully, and emits a tremendous number of plots. For every annotation used in clustering, the distributions and pair-wise comparison (with ellipses denoting the 2-sigma cluster boundaries) are shown. Each cluster is shaded with a color proportional to its mixture coefficient. To use this module, you'll first have to take your VCF and create an R-readable table out of it with the following command: python /path/to/Sting/trunk/python/vcf2table.py -f CHROM,POS,ID,AC,AF,AN,DB,DP,HRun,MQ,MQ0,MyHaplotypeScore,QD,SB my.vcf > my.vcf.table Then, simply invoke this module with the command: Rscript /path/to/Sting/trunk/R/VariantRecalibratorReport/VariantRecalibratorReport.R /path/to/output/prefix /path/to/my/my.clusters /path/to/my.vcf.table [/path/to/my.suspicious.loci] This will create a number of plots all with the prefix "/path/to/output/prefix". For instance, if you used QD, SB, HRun, and MyHaplotypeScore annotations during clustering, you should see output like this: /path/to/output/prefix.anndist.HRun.pdf /path/to/output/prefix.anndist.MyHaplotypeScore.pdf /path/to/output/prefix.anndist.QD.pdf /path/to/output/prefix.anndist.SB.pdf /path/to/output/prefix.cluster.HRun_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.HRun_vs_QD.pdf /path/to/output/prefix.cluster.HRun_vs_SB.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_HRun.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_QD.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_SB.pdf /path/to/output/prefix.cluster.QD_vs_HRun.pdf /path/to/output/prefix.cluster.QD_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.QD_vs_SB.pdf /path/to/output/prefix.cluster.SB_vs_HRun.pdf /path/to/output/prefix.cluster.SB_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.SB_vs_QD.pdf git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3936 348d0f76-0448-11de-a6fe-93d51630548a
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library(ellipse);
library(hexbin);
library(rgl);
args = commandArgs(TRUE);
plotRoot = args[1];
if (is.na(plotRoot)) { plotRoot = "test"; }
clusterFile = args[2];
if (is.na(clusterFile)) { clusterFile = "/home/radon01/depristo/work/oneOffProjects/1000GenomesProcessingPaper/wgs.v7/GA2.WEx.cleaned.ug.snpfiltered.indelfiltered.optimized"; }
vcfTable = args[3];
if (is.na(vcfTable)) { vcfTable = "/home/radon01/kiran/scr1/projects/DataProcessingPaper/scratch/MarkBustedWEx.table"; }
lociFile = args[4];
if (is.na(lociFile) | lociFile == "NA" ) { lociFile = "/home/radon01/kiran/scr1/projects/DataProcessingPaper/scratch/MarkBustedWEx.loci"; }
An R module that takes in a Variant Recalibration cluster file (file with '@!CLUSTER' lines in it), a tabularized VCF, and optionally a set of loci that should be examined more carefully, and emits a tremendous number of plots. For every annotation used in clustering, the distributions and pair-wise comparison (with ellipses denoting the 2-sigma cluster boundaries) are shown. Each cluster is shaded with a color proportional to its mixture coefficient. To use this module, you'll first have to take your VCF and create an R-readable table out of it with the following command: python /path/to/Sting/trunk/python/vcf2table.py -f CHROM,POS,ID,AC,AF,AN,DB,DP,HRun,MQ,MQ0,MyHaplotypeScore,QD,SB my.vcf > my.vcf.table Then, simply invoke this module with the command: Rscript /path/to/Sting/trunk/R/VariantRecalibratorReport/VariantRecalibratorReport.R /path/to/output/prefix /path/to/my/my.clusters /path/to/my.vcf.table [/path/to/my.suspicious.loci] This will create a number of plots all with the prefix "/path/to/output/prefix". For instance, if you used QD, SB, HRun, and MyHaplotypeScore annotations during clustering, you should see output like this: /path/to/output/prefix.anndist.HRun.pdf /path/to/output/prefix.anndist.MyHaplotypeScore.pdf /path/to/output/prefix.anndist.QD.pdf /path/to/output/prefix.anndist.SB.pdf /path/to/output/prefix.cluster.HRun_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.HRun_vs_QD.pdf /path/to/output/prefix.cluster.HRun_vs_SB.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_HRun.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_QD.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_SB.pdf /path/to/output/prefix.cluster.QD_vs_HRun.pdf /path/to/output/prefix.cluster.QD_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.QD_vs_SB.pdf /path/to/output/prefix.cluster.SB_vs_HRun.pdf /path/to/output/prefix.cluster.SB_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.SB_vs_QD.pdf git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3936 348d0f76-0448-11de-a6fe-93d51630548a
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maxVariants = args[5];
if (is.na(maxVariants)) { maxVariants = -1; }
maxVariants = as.integer(maxVariants)
An R module that takes in a Variant Recalibration cluster file (file with '@!CLUSTER' lines in it), a tabularized VCF, and optionally a set of loci that should be examined more carefully, and emits a tremendous number of plots. For every annotation used in clustering, the distributions and pair-wise comparison (with ellipses denoting the 2-sigma cluster boundaries) are shown. Each cluster is shaded with a color proportional to its mixture coefficient. To use this module, you'll first have to take your VCF and create an R-readable table out of it with the following command: python /path/to/Sting/trunk/python/vcf2table.py -f CHROM,POS,ID,AC,AF,AN,DB,DP,HRun,MQ,MQ0,MyHaplotypeScore,QD,SB my.vcf > my.vcf.table Then, simply invoke this module with the command: Rscript /path/to/Sting/trunk/R/VariantRecalibratorReport/VariantRecalibratorReport.R /path/to/output/prefix /path/to/my/my.clusters /path/to/my.vcf.table [/path/to/my.suspicious.loci] This will create a number of plots all with the prefix "/path/to/output/prefix". For instance, if you used QD, SB, HRun, and MyHaplotypeScore annotations during clustering, you should see output like this: /path/to/output/prefix.anndist.HRun.pdf /path/to/output/prefix.anndist.MyHaplotypeScore.pdf /path/to/output/prefix.anndist.QD.pdf /path/to/output/prefix.anndist.SB.pdf /path/to/output/prefix.cluster.HRun_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.HRun_vs_QD.pdf /path/to/output/prefix.cluster.HRun_vs_SB.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_HRun.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_QD.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_SB.pdf /path/to/output/prefix.cluster.QD_vs_HRun.pdf /path/to/output/prefix.cluster.QD_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.QD_vs_SB.pdf /path/to/output/prefix.cluster.SB_vs_HRun.pdf /path/to/output/prefix.cluster.SB_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.SB_vs_QD.pdf git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3936 348d0f76-0448-11de-a6fe-93d51630548a
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getAnnIndex <- function(d, ann) {
index = -1;
for (i in c(1:length(names(d)))) {
if (names(d)[i] == ann) {
index = i;
}
}
index;
}
getClusterAnnIndex <- function(c, ann) {
index = -1;
for (i in c(1:length(c[[1]]$anns))) {
if (c[[1]]$anns[i] == ann) {
index = i;
}
}
index;
}
plotAnn <- function(d.known, d.novel, d.loci, ann, plotfile) {
index = getAnnIndex(d.known, ann);
k = hist(d.known[,index], breaks=100, plot=FALSE);
n = hist(d.novel[,index], breaks=100, plot=FALSE);
pdf(plotfile);
plot(k$mids, k$density, type="b", col="blue", ylim=c(0, max(k$density)), lwd=2, xlab=ann, ylab="Density", bty="n");
points(n$mids, n$density, type="b", col="red", lwd=2);
if (!is.na(d.loci)) {
legend("topright", c("Known", "Novel", "Suspicious loci"), col=c("blue", "red", "yellow3"), pch=c(21, 21, 18));
} else {
legend("topright", c("Known", "Novel"), col=c("blue", "red"), pch=21);
}
if (!is.na(d.loci)) {
for (i in c(1:nrow(d.loci))) {
points(d.loci[i, index], 0, col="yellow3", pch=18, cex=2.0);
}
}
dev.off();
}
read.clusters <- function(filename) {
con = file(filename, "r", blocking = FALSE)
lines = readLines(con)
close(con);
anns = c();
annIndex = 1;
clusterIndex = 1;
clusters = c();
conversions = c();
for (line in lines) {
if (length(grep("ANNOTATION", line)) > 0) {
linePieces = unlist(strsplit(line, ","));
anns = c(anns, linePieces[2]);
conversions[[annIndex]] = list(ann = linePieces[2], offset = as.numeric(linePieces[3]), multiplier = as.numeric(linePieces[4]));
annIndex = annIndex + 1;
} else if (length(grep("CLUSTER", line)) > 0) {
linePieces = unlist(strsplit(line, ","));
mixtureWeight = linePieces[2];
mu = linePieces[3:(3+length(anns)-1)];
cov = linePieces[(3+length(anns)):length(linePieces)];
clusters[[clusterIndex]] = list(
anns = anns,
conversions = conversions,
mixtureWeight = as.numeric(mixtureWeight),
means = as.numeric(mu),
cov = matrix(cov, nrow=length(anns), ncol=length(anns))
);
clusterIndex = clusterIndex + 1;
}
}
clusters;
}
plotClusters <- function(d.known, d.novel, d.loci, c, ann1, ann2, filename, maxVariants = -1) {
index1 = getAnnIndex(d.known, ann1);
index2 = getAnnIndex(d.known, ann2);
cindex1 = getClusterAnnIndex(c, ann1);
cindex2 = getClusterAnnIndex(c, ann2);
mult1 = c[[1]]$conversions[[cindex1]]$multiplier;
off1 = c[[1]]$conversions[[cindex1]]$offset;
mult2 = c[[1]]$conversions[[cindex2]]$multiplier;
off2 = c[[1]]$conversions[[cindex2]]$offset;
# todo -- should only include min/max actually observed if bounds are bigger than actual distributions
xvalsForLims = c(-5, 5)
yvalsForLims = c(-5, 5)
#xvalsForLims = (d.known[,index1] - off1)/mult1
#yvalsForLims = (d.known[,index2] - off2)/mult2
xlims = c(min(xvalsForLims), 1.2*max(xvalsForLims));
ylims = c(min(yvalsForLims), max(yvalsForLims));
An R module that takes in a Variant Recalibration cluster file (file with '@!CLUSTER' lines in it), a tabularized VCF, and optionally a set of loci that should be examined more carefully, and emits a tremendous number of plots. For every annotation used in clustering, the distributions and pair-wise comparison (with ellipses denoting the 2-sigma cluster boundaries) are shown. Each cluster is shaded with a color proportional to its mixture coefficient. To use this module, you'll first have to take your VCF and create an R-readable table out of it with the following command: python /path/to/Sting/trunk/python/vcf2table.py -f CHROM,POS,ID,AC,AF,AN,DB,DP,HRun,MQ,MQ0,MyHaplotypeScore,QD,SB my.vcf > my.vcf.table Then, simply invoke this module with the command: Rscript /path/to/Sting/trunk/R/VariantRecalibratorReport/VariantRecalibratorReport.R /path/to/output/prefix /path/to/my/my.clusters /path/to/my.vcf.table [/path/to/my.suspicious.loci] This will create a number of plots all with the prefix "/path/to/output/prefix". For instance, if you used QD, SB, HRun, and MyHaplotypeScore annotations during clustering, you should see output like this: /path/to/output/prefix.anndist.HRun.pdf /path/to/output/prefix.anndist.MyHaplotypeScore.pdf /path/to/output/prefix.anndist.QD.pdf /path/to/output/prefix.anndist.SB.pdf /path/to/output/prefix.cluster.HRun_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.HRun_vs_QD.pdf /path/to/output/prefix.cluster.HRun_vs_SB.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_HRun.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_QD.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_SB.pdf /path/to/output/prefix.cluster.QD_vs_HRun.pdf /path/to/output/prefix.cluster.QD_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.QD_vs_SB.pdf /path/to/output/prefix.cluster.SB_vs_HRun.pdf /path/to/output/prefix.cluster.SB_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.SB_vs_QD.pdf git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3936 348d0f76-0448-11de-a6fe-93d51630548a
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clusterColors = c("#A62103", "#F27405", "#F29F05", "#F2B705", "#F2CB05");
pdf(filename);
par(mar=c(5, 6, 2, 5));
plot(0, 0, type="n", xaxt="n", yaxt="n", xlim=xlims, ylim=ylims, xlab=ann1, ylab=ann2, bty="n");
mv.known = if (maxVariants == -1 | maxVariants >= nrow(d.known)) { seq(1, nrow(d.known)) } else { as.integer(runif(maxVariants, 1, nrow(d.known)+1))}
mv.novel = if (maxVariants == -1 | maxVariants >= nrow(d.novel)) { 1:nrow(d.novel) } else { as.integer(runif(maxVariants, 1, nrow(d.novel)+1)) }
print(dim(mv.known))
print(maxVariants)
points(((d.known[,index1] - off1)/mult1)[mv.known], ((d.known[,index2] - off2)/mult2)[mv.known], pch=19, cex=0.3, col="#0000FF33");
points(((d.novel[,index1] - off1)/mult1)[mv.novel], ((d.novel[,index2] - off2)/mult2)[mv.novel], pch=19, cex=0.3, col="#FF000033");
An R module that takes in a Variant Recalibration cluster file (file with '@!CLUSTER' lines in it), a tabularized VCF, and optionally a set of loci that should be examined more carefully, and emits a tremendous number of plots. For every annotation used in clustering, the distributions and pair-wise comparison (with ellipses denoting the 2-sigma cluster boundaries) are shown. Each cluster is shaded with a color proportional to its mixture coefficient. To use this module, you'll first have to take your VCF and create an R-readable table out of it with the following command: python /path/to/Sting/trunk/python/vcf2table.py -f CHROM,POS,ID,AC,AF,AN,DB,DP,HRun,MQ,MQ0,MyHaplotypeScore,QD,SB my.vcf > my.vcf.table Then, simply invoke this module with the command: Rscript /path/to/Sting/trunk/R/VariantRecalibratorReport/VariantRecalibratorReport.R /path/to/output/prefix /path/to/my/my.clusters /path/to/my.vcf.table [/path/to/my.suspicious.loci] This will create a number of plots all with the prefix "/path/to/output/prefix". For instance, if you used QD, SB, HRun, and MyHaplotypeScore annotations during clustering, you should see output like this: /path/to/output/prefix.anndist.HRun.pdf /path/to/output/prefix.anndist.MyHaplotypeScore.pdf /path/to/output/prefix.anndist.QD.pdf /path/to/output/prefix.anndist.SB.pdf /path/to/output/prefix.cluster.HRun_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.HRun_vs_QD.pdf /path/to/output/prefix.cluster.HRun_vs_SB.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_HRun.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_QD.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_SB.pdf /path/to/output/prefix.cluster.QD_vs_HRun.pdf /path/to/output/prefix.cluster.QD_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.QD_vs_SB.pdf /path/to/output/prefix.cluster.SB_vs_HRun.pdf /path/to/output/prefix.cluster.SB_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.SB_vs_QD.pdf git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3936 348d0f76-0448-11de-a6fe-93d51630548a
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for (clusterIndex in c(1:length(c))) {
mu = c(c[[clusterIndex]]$means[cindex1], c[[clusterIndex]]$means[cindex2]);
cov = matrix(as.numeric(
matrix(
c(
c[[clusterIndex]]$cov[cindex1,cindex1],
c[[clusterIndex]]$cov[cindex2,cindex1],
c[[clusterIndex]]$cov[cindex1,cindex2],
c[[clusterIndex]]$cov[cindex2,cindex2]
),
nrow=2, ncol=2
)
), nrow=2, ncol=2
);
weight = c[[clusterIndex]]$mixtureWeight;
if (weight <= 0.20) { color = clusterColors[1]; }
else if (weight > 0.20 && weight <= 0.40) { color = clusterColors[2]; }
else if (weight > 0.40 && weight <= 0.60) { color = clusterColors[3]; }
else if (weight > 0.60 && weight <= 0.80) { color = clusterColors[4]; }
else if (weight > 0.80) { color = clusterColors[5]; }
lineweight = ifelse(weight > 0.50, 4, 3);
An R module that takes in a Variant Recalibration cluster file (file with '@!CLUSTER' lines in it), a tabularized VCF, and optionally a set of loci that should be examined more carefully, and emits a tremendous number of plots. For every annotation used in clustering, the distributions and pair-wise comparison (with ellipses denoting the 2-sigma cluster boundaries) are shown. Each cluster is shaded with a color proportional to its mixture coefficient. To use this module, you'll first have to take your VCF and create an R-readable table out of it with the following command: python /path/to/Sting/trunk/python/vcf2table.py -f CHROM,POS,ID,AC,AF,AN,DB,DP,HRun,MQ,MQ0,MyHaplotypeScore,QD,SB my.vcf > my.vcf.table Then, simply invoke this module with the command: Rscript /path/to/Sting/trunk/R/VariantRecalibratorReport/VariantRecalibratorReport.R /path/to/output/prefix /path/to/my/my.clusters /path/to/my.vcf.table [/path/to/my.suspicious.loci] This will create a number of plots all with the prefix "/path/to/output/prefix". For instance, if you used QD, SB, HRun, and MyHaplotypeScore annotations during clustering, you should see output like this: /path/to/output/prefix.anndist.HRun.pdf /path/to/output/prefix.anndist.MyHaplotypeScore.pdf /path/to/output/prefix.anndist.QD.pdf /path/to/output/prefix.anndist.SB.pdf /path/to/output/prefix.cluster.HRun_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.HRun_vs_QD.pdf /path/to/output/prefix.cluster.HRun_vs_SB.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_HRun.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_QD.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_SB.pdf /path/to/output/prefix.cluster.QD_vs_HRun.pdf /path/to/output/prefix.cluster.QD_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.QD_vs_SB.pdf /path/to/output/prefix.cluster.SB_vs_HRun.pdf /path/to/output/prefix.cluster.SB_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.SB_vs_QD.pdf git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3936 348d0f76-0448-11de-a6fe-93d51630548a
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points(mu[1], mu[2], pch=21, col=color, cex=0.5);
points(ellipse(t(cov), centre=mu), type="l", lwd=lineweight, col=color);
}
axis(1,
labels=as.integer(seq(from=min(d.novel[,index1]), to=max(d.novel[,index1]), by=(abs(min(d.novel[,index1])) + abs(max(d.novel[,index1])))/5)),
at=seq(from=min((d.novel[,index1] - off1)/mult1), to=max((d.novel[,index1] - off1)/mult1), by=(abs(min((d.novel[,index1] - off1)/mult1)) + abs(max((d.novel[,index1] - off1)/mult1)))/5)
);
axis(2,
labels=as.integer(seq(from=min(d.novel[,index2]), to=max(d.novel[,index2]), by=(abs(min(d.novel[,index2])) + abs(max(d.novel[,index2])))/5)),
at=seq(from=min((d.novel[,index2] - off2)/mult2), to=max((d.novel[,index2] - off2)/mult2), by=(abs(min((d.novel[,index2] - off2)/mult2)) + abs(max((d.novel[,index2] - off2)/mult2)))/5)
);
if (!is.na(d.loci)) {
legend("bottomleft", c("Known", "Novel", "Suspicious loci"), col=c("blue", "red", "yellow3"), pch=19);
} else {
legend("bottomleft", c("Known", "Novel"), col=c("blue", "red"), pch=19);
}
pieces = 100;
scale = ((abs(ylims[1]) + abs(ylims[2]))/pieces);
width = ((abs(xlims[1]) + abs(xlims[2]))/12);
offset = ylims[1];
for (i in c(1:pieces)) {
color = clusterColors[1];
if (i <= 20) { color = clusterColors[1]; }
else if (i > 20 && i <= 40) { color = clusterColors[2]; }
else if (i > 40 && i <= 60) { color = clusterColors[3]; }
else if (i > 60 && i <= 80) { color = clusterColors[4]; }
else if (i > 80) { color = clusterColors[5]; }
polygon(x=xlims[2] + c(0, 0, width, width), y=offset + scale*c((i-1), (i), (i), (i-1)), col=color, border=color);
}
axis(4, labels=c(0.0, 0.20, 0.40, 0.60, 0.80, 1.0), at=c(ylims[1], ylims[1] + 20*scale, ylims[1] + 40*scale, ylims[1] + 60*scale, ylims[1] + 80*scale, ylims[2]));
mtext("Mixture coefficient", 4, line=3);
if (!is.na(d.loci)) {
points((d.loci[,index1] - off1)/mult1, (d.loci[,index2] - off2)/mult2, pch=19, cex=0.8, col="yellow3");
}
dev.off();
}
l = c();
if (!is.na(lociFile)) {
t = read.table(lociFile, header=TRUE);
l = t$POS;
}
d = read.table(vcfTable, header=TRUE);
c = read.clusters(clusterFile);
An R module that takes in a Variant Recalibration cluster file (file with '@!CLUSTER' lines in it), a tabularized VCF, and optionally a set of loci that should be examined more carefully, and emits a tremendous number of plots. For every annotation used in clustering, the distributions and pair-wise comparison (with ellipses denoting the 2-sigma cluster boundaries) are shown. Each cluster is shaded with a color proportional to its mixture coefficient. To use this module, you'll first have to take your VCF and create an R-readable table out of it with the following command: python /path/to/Sting/trunk/python/vcf2table.py -f CHROM,POS,ID,AC,AF,AN,DB,DP,HRun,MQ,MQ0,MyHaplotypeScore,QD,SB my.vcf > my.vcf.table Then, simply invoke this module with the command: Rscript /path/to/Sting/trunk/R/VariantRecalibratorReport/VariantRecalibratorReport.R /path/to/output/prefix /path/to/my/my.clusters /path/to/my.vcf.table [/path/to/my.suspicious.loci] This will create a number of plots all with the prefix "/path/to/output/prefix". For instance, if you used QD, SB, HRun, and MyHaplotypeScore annotations during clustering, you should see output like this: /path/to/output/prefix.anndist.HRun.pdf /path/to/output/prefix.anndist.MyHaplotypeScore.pdf /path/to/output/prefix.anndist.QD.pdf /path/to/output/prefix.anndist.SB.pdf /path/to/output/prefix.cluster.HRun_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.HRun_vs_QD.pdf /path/to/output/prefix.cluster.HRun_vs_SB.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_HRun.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_QD.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_SB.pdf /path/to/output/prefix.cluster.QD_vs_HRun.pdf /path/to/output/prefix.cluster.QD_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.QD_vs_SB.pdf /path/to/output/prefix.cluster.SB_vs_HRun.pdf /path/to/output/prefix.cluster.SB_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.SB_vs_QD.pdf git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3936 348d0f76-0448-11de-a6fe-93d51630548a
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d.known = d[which(d$DB == 1),];
d.novel = d[which(d$DB == 0),];
d.loci = NA;
if (length(l) > 0) {
d.loci = d[which(d$POS %in% l),];
}
for (ann1 in c[[1]]$anns) {
print(ann1)
An R module that takes in a Variant Recalibration cluster file (file with '@!CLUSTER' lines in it), a tabularized VCF, and optionally a set of loci that should be examined more carefully, and emits a tremendous number of plots. For every annotation used in clustering, the distributions and pair-wise comparison (with ellipses denoting the 2-sigma cluster boundaries) are shown. Each cluster is shaded with a color proportional to its mixture coefficient. To use this module, you'll first have to take your VCF and create an R-readable table out of it with the following command: python /path/to/Sting/trunk/python/vcf2table.py -f CHROM,POS,ID,AC,AF,AN,DB,DP,HRun,MQ,MQ0,MyHaplotypeScore,QD,SB my.vcf > my.vcf.table Then, simply invoke this module with the command: Rscript /path/to/Sting/trunk/R/VariantRecalibratorReport/VariantRecalibratorReport.R /path/to/output/prefix /path/to/my/my.clusters /path/to/my.vcf.table [/path/to/my.suspicious.loci] This will create a number of plots all with the prefix "/path/to/output/prefix". For instance, if you used QD, SB, HRun, and MyHaplotypeScore annotations during clustering, you should see output like this: /path/to/output/prefix.anndist.HRun.pdf /path/to/output/prefix.anndist.MyHaplotypeScore.pdf /path/to/output/prefix.anndist.QD.pdf /path/to/output/prefix.anndist.SB.pdf /path/to/output/prefix.cluster.HRun_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.HRun_vs_QD.pdf /path/to/output/prefix.cluster.HRun_vs_SB.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_HRun.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_QD.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_SB.pdf /path/to/output/prefix.cluster.QD_vs_HRun.pdf /path/to/output/prefix.cluster.QD_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.QD_vs_SB.pdf /path/to/output/prefix.cluster.SB_vs_HRun.pdf /path/to/output/prefix.cluster.SB_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.SB_vs_QD.pdf git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3936 348d0f76-0448-11de-a6fe-93d51630548a
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plotAnn(d.known, d.novel, d.loci, ann1, paste(plotRoot, ".anndist.", ann1, ".pdf", sep=""));
for (ann2 in c[[1]]$anns) {
if (ann1 != ann2) {
print(paste("-- v ", ann2))
plotClusters(d.known, d.novel, d.loci, c, ann1, ann2, paste(plotRoot, ".cluster.", ann1, "_vs_", ann2, ".pdf", sep=""), maxVariants=maxVariants);
An R module that takes in a Variant Recalibration cluster file (file with '@!CLUSTER' lines in it), a tabularized VCF, and optionally a set of loci that should be examined more carefully, and emits a tremendous number of plots. For every annotation used in clustering, the distributions and pair-wise comparison (with ellipses denoting the 2-sigma cluster boundaries) are shown. Each cluster is shaded with a color proportional to its mixture coefficient. To use this module, you'll first have to take your VCF and create an R-readable table out of it with the following command: python /path/to/Sting/trunk/python/vcf2table.py -f CHROM,POS,ID,AC,AF,AN,DB,DP,HRun,MQ,MQ0,MyHaplotypeScore,QD,SB my.vcf > my.vcf.table Then, simply invoke this module with the command: Rscript /path/to/Sting/trunk/R/VariantRecalibratorReport/VariantRecalibratorReport.R /path/to/output/prefix /path/to/my/my.clusters /path/to/my.vcf.table [/path/to/my.suspicious.loci] This will create a number of plots all with the prefix "/path/to/output/prefix". For instance, if you used QD, SB, HRun, and MyHaplotypeScore annotations during clustering, you should see output like this: /path/to/output/prefix.anndist.HRun.pdf /path/to/output/prefix.anndist.MyHaplotypeScore.pdf /path/to/output/prefix.anndist.QD.pdf /path/to/output/prefix.anndist.SB.pdf /path/to/output/prefix.cluster.HRun_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.HRun_vs_QD.pdf /path/to/output/prefix.cluster.HRun_vs_SB.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_HRun.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_QD.pdf /path/to/output/prefix.cluster.MyHaplotypeScore_vs_SB.pdf /path/to/output/prefix.cluster.QD_vs_HRun.pdf /path/to/output/prefix.cluster.QD_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.QD_vs_SB.pdf /path/to/output/prefix.cluster.SB_vs_HRun.pdf /path/to/output/prefix.cluster.SB_vs_MyHaplotypeScore.pdf /path/to/output/prefix.cluster.SB_vs_QD.pdf git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@3936 348d0f76-0448-11de-a6fe-93d51630548a
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}
}
}