Last updated: 2018-06-05
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File | Version | Author | Date | Message |
---|---|---|---|---|
Rmd | 35816c4 | Peter Carbonetto | 2018-06-05 | wflow_publish(“SharingMag.Rmd”) |
Rmd | 747f788 | Peter Carbonetto | 2018-06-05 | Rebuilt SharingSign page after renaming and other improvements. |
html | 747f788 | Peter Carbonetto | 2018-06-05 | Rebuilt SharingSign page after renaming and other improvements. |
The plot generated here summarizes eQTL sharing by magnitude between all pairs of tissues. Compare against Figure 6 of the paper.
First, we load the lattice package used for generating the plot below.
library(lattice)
In the next code chunk, we load some GTEx summary statistics, as well as some of the results generated from the mash analysis of the GTEx data.
out <- readRDS("../data/MatrixEQTLSumStats.Portable.Z.rds")
maxb <- out$test.b
maxz <- out$test.z
out <-readRDS(paste("../output/MatrixEQTLSumStats.Portable.Z.coved.K3.P3",
"lite.single.expanded.V1.posterior.rds",sep = "."))
pm.mash <- out$posterior.means
lfsr.all <- out$lfsr
standard.error <- maxb/maxz
pm.mash.beta <- pm.mash*standard.error
For every pair of tissues, we count the proportion of effects significant in either tissue that are within 2-fold magnitude of one another.
thresh <- 0.05
pm.mash.beta <- pm.mash.beta[rowSums(lfsr.all<0.05)>0,]
lfsr.mash <- lfsr.all[rowSums(lfsr.all<0.05)>0,]
shared.fold.size <- matrix(NA,nrow = ncol(lfsr.mash),ncol=ncol(lfsr.mash))
colnames(shared.fold.size) <- rownames(shared.fold.size) <- colnames(maxz)
for (i in 1:ncol(lfsr.mash))
for (j in 1:ncol(lfsr.mash)) {
sig.row=which(lfsr.mash[,i]<thresh)
sig.col=which(lfsr.mash[,j]<thresh)
a=(union(sig.row,sig.col))
quotient=(pm.mash.beta[a,i]/pm.mash.beta[a,j])
shared.fold.size[i,j] = mean(quotient > 0.5 & quotient < 2)
}
Generate the heatmap using the “levelplot” function from the lattice package.
all.tissue.order <- read.table("../data/alltissueorder.txt")[,1]
clrs <- colorRampPalette(rev(c("#D73027","#FC8D59","#FEE090","#FFFFBF",
"#E0F3F8","#91BFDB","#4575B4")))(64)
lat <- shared.fold.size[rev(all.tissue.order),rev(all.tissue.order)]
lat[lower.tri(lat)] <- NA
n <- nrow(lat)
print(levelplot(lat[n:1,],col.regions = clrs,xlab = "",ylab = "",
colorkey = TRUE))
Version | Author | Date |
---|---|---|
747f788 | Peter Carbonetto | 2018-06-05 |
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
#
# Matrix products: default
# BLAS: /Library/Frameworks/R.framework/Versions/3.4/Resources/lib/libRblas.0.dylib
# LAPACK: /Library/Frameworks/R.framework/Versions/3.4/Resources/lib/libRlapack.dylib
#
# locale:
# [1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8
#
# attached base packages:
# [1] stats graphics grDevices utils datasets methods base
#
# other attached packages:
# [1] lattice_0.20-35
#
# loaded via a namespace (and not attached):
# [1] workflowr_1.0.1.9000 Rcpp_0.12.16 digest_0.6.15
# [4] rprojroot_1.3-2 R.methodsS3_1.7.1 grid_3.4.3
# [7] backports_1.1.2 git2r_0.21.0 magrittr_1.5
# [10] evaluate_0.10.1 stringi_1.1.7 whisker_0.3-2
# [13] R.oo_1.21.0 R.utils_2.6.0 rmarkdown_1.9
# [16] tools_3.4.3 stringr_1.3.0 yaml_2.1.18
# [19] compiler_3.4.3 htmltools_0.3.6 knitr_1.20
This reproducible R Markdown analysis was created with workflowr 1.0.1.9000