Last updated: 2018-06-05
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Rmd | 4a93c87 | Peter Carbonetto | 2018-06-05 | wflow_publish(“ExpressionAnalysis.Rmd”) |
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Rmd | 0a5d3bc | Peter Carbonetto | 2018-06-05 | Renamed Fig.ExpressionAnalysis.Rmd as ExpressionAnalysis.Rmd. |
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In this analysis, we assess whether tissue-specific eQTLs we identified can be explained by tissue-specific expression. Specifically, we take genes with tissue-specific eQTLs, and examine the distribution of expression in the eQTL-affected tissue relative to expression in other tissues.
In the next code chunk, we load some GTEx summary statistics (average gene expression values and z-scores), as well as some of the results generated from the mash analysis of the GTEx data.
Expression is here defined as median across individuals of the log Reads per Kilobase Mapped (RPKM).
data <- read.csv("../data/AvgExpr.csv.gz",header = TRUE)
out <- readRDS("../data/MatrixEQTLSumStats.Portable.Z.rds")
maxz <- out$test.z
qtl.names <-
sapply(1:length(rownames(maxz)),
function(x) unlist(strsplit(rownames(maxz)[x], "[_]"))[[1]])
rownames(data) <- data[,1]
expr.data <- data[,-1]
out <- readRDS(paste("../output/MatrixEQTLSumStats.Portable.Z.coved.K3.P3",
"lite.single.expanded.V1.posterior.rds",sep = "."))
pmash <- out$posterior.means
lfsr <- out$lfsr
colnames(lfsr) <- colnames(pmash) <- colnames(maxz)
rownames(lfsr) <- rownames(pmash) <- rownames(maxz)
expr.sort <- expr.data[rownames(expr.data)%in%qtl.names,]
a <- match(qtl.names,rownames(expr.sort))
expr.sort <- expr.sort[a,]
missing.tissues <- c(7,8,19,20,24,25,31,34,37)
exp.sort <- expr.sort[,-missing.tissues]
colnames(exp.sort) <- colnames(maxz)
Here we define a couple functions used to compare the densities and CDFs of gene expression levels.
plot_tissuespecifictwo = function(tissuename,lfsr,ymax,curvedata,title,
thresh=0.05,subset=1:44,exclude=0.01) {
index_tissue=which(colnames(lfsr) %in% tissuename);
ybar=title
# Create a matrix showing whether or not lfsr satisfies threshold.
sigmat = lfsr <= thresh;
sigs=which(rowSums(sigmat[,index_tissue,drop=FALSE])==length(tissuename) &
rowSums(sigmat[,-index_tissue,drop=FALSE])==0)
norm.spec=density(curvedata[sigs,index_tissue])
norm.other=density(curvedata[-sigs,index_tissue])
xmin=min(norm.spec$x,norm.other$x)-1
ymin=min(norm.spec$y,norm.other$y)
xmax=max(norm.spec$x,norm.other$x)+1
plot(norm.other,xlim = c(xmin,xmax),ylim=c(0,ymax),
col="black",main=tissuename,xlab="log(RPKM)")
lines(norm.spec,col="red")
legend("right",legend = c("All Genes","Tissue Specific"),
col=c("black","red"),pch=c(1,1))
}
plot_tissuespecificthree = function(tissuename,lfsr,ymax,curvedata,title,
thresh=0.05,subset=1:44,exclude=0.01) {
index_tissue=which(colnames(lfsr) %in% tissuename);
ybar=title
# Create a matrix showing whether or not lfsr satisfies threshold.
sigmat = lfsr <= thresh
sigs=which(rowSums(sigmat[,index_tissue,drop=FALSE])==length(tissuename) &
rowSums(sigmat[,-index_tissue,drop=FALSE])==0)
norm.spec=ecdf(curvedata[sigs,index_tissue])
norm.other=ecdf(curvedata[-sigs,index_tissue])
plot(norm.other,ylim=c(0,ymax),
col="black",main=tissuename,xlab="log(RPKM)")
lines(norm.spec,col="red",cex=0.1)
legend("right",legend = c("All Genes","Tissue Specific"),
col=c("black","red"),pch=c(1,1))
}
The two plots below compare the densities and cumulative distribution functions of the expression levels for all genes (black), and for genes identified as having a “tissue-specific” eQTL (red) in testis.
plot_tissuespecifictwo(tissuename = "Testis",lfsr = lfsr,
curvedata = log(exp.sort),title = "Test",
thresh = 0.05 ,ymax=0.5)
Version | Author | Date |
---|---|---|
0a5d3bc | Peter Carbonetto | 2018-06-05 |
plot_tissuespecificthree(tissuename = "Testis",lfsr = lfsr,
curvedata = log(exp.sort),title = "Test",
thresh = 0.05 ,ymax=1)
Version | Author | Date |
---|---|---|
0a5d3bc | Peter Carbonetto | 2018-06-05 |
The distribution functions are reasonably similar.
Next we show the same two plots for thyroid.
plot_tissuespecifictwo(tissuename = "Thyroid",lfsr = lfsr,
curvedata = log(exp.sort),title = "Test",
thresh = 0.05,ymax = 0.5)
Version | Author | Date |
---|---|---|
0a5d3bc | Peter Carbonetto | 2018-06-05 |
plot_tissuespecificthree(tissuename = "Thyroid",lfsr = lfsr,
curvedata = log(exp.sort),title = "Test",
thresh = 0.05,ymax = 1)
Version | Author | Date |
---|---|---|
0a5d3bc | Peter Carbonetto | 2018-06-05 |
Next, we look at the distributions in whole blood cells.
plot_tissuespecifictwo(tissuename = "Whole_Blood",lfsr = lfsr,
curvedata = log(exp.sort),title = "Test",
thresh = 0.05,ymax=0.5)
Version | Author | Date |
---|---|---|
0a5d3bc | Peter Carbonetto | 2018-06-05 |
plot_tissuespecificthree(tissuename = "Whole_Blood",lfsr = lfsr,
curvedata = log(exp.sort),title = "Test",
thresh = 0.05 ,ymax=1)
Version | Author | Date |
---|---|---|
0a5d3bc | Peter Carbonetto | 2018-06-05 |
Finally, we examine the gene expression distributions in fibroblasts.
plot_tissuespecifictwo(tissuename = "Cells_Transformed_fibroblasts",
lfsr = lfsr,curvedata = log(exp.sort),title = "Test",
thresh = 0.05,ymax=0.5)
Version | Author | Date |
---|---|---|
0a5d3bc | Peter Carbonetto | 2018-06-05 |
plot_tissuespecificthree(tissuename = "Cells_Transformed_fibroblasts",
lfsr = lfsr,curvedata = log(exp.sort),title = "Test",
thresh = 0.05 ,ymax=1)
Version | Author | Date |
---|---|---|
0a5d3bc | Peter Carbonetto | 2018-06-05 |
In each case, the distribution functions are similar. This tells us that tissue-specific eQTLs are not simply reflecting tissue-specific expression.
sessionInfo()
# R version 3.4.3 (2017-11-30)
# Platform: x86_64-apple-darwin15.6.0 (64-bit)
# Running under: macOS High Sierra 10.13.4
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# LAPACK: /Library/Frameworks/R.framework/Versions/3.4/Resources/lib/libRlapack.dylib
#
# locale:
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# attached base packages:
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#
# loaded via a namespace (and not attached):
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