Last updated: 2018-06-18
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File | Version | Author | Date | Message |
---|---|---|---|---|
Rmd | 70b3ae5 | Gao Wang | 2018-06-16 | Fix misplaced strong.s labels |
Rmd | 6314ce0 | Gao Wang | 2018-06-16 | Relabel ‘test’ to ‘strong’ in data and code |
html | e9c2b58 | Peter Carbonetto | 2018-06-05 | Re-built Uk* webpages after minor revisions. |
html | f01cfd4 | Peter Carbonetto | 2018-06-05 | Re-built Uk3 and Uk4 webpages after renaming the R Markdown files. |
Rmd | f94acfb | Peter Carbonetto | 2018-06-05 | wflow_publish(c(“Uk3.Rmd”, “Uk4.Rmd”)) |
html | aecc7f1 | Peter Carbonetto | 2017-09-20 | Moved doc to docs. |
Rmd | 7072cdb | Peter Carbonetto | 2017-09-20 | Reorganized many of the files. |
“Uk3” is the covariance matrix corresponding to the output of the ExtremeDeconvolution algorithm that was initialized with the rank3 SVD approximation of \(X^TX\). It is the pattern of sharing identified from the dominant covariance matrix (the one with the largest mixture weight).
Here we plot the correlation matrix and the first 3 eigenvectors of “Uk3”. This provides a visualization of the primary patterns of genetic sharing identified by our method, mash. This code should closely reproduce Figure 3 of the paper.
First, we load a couple plotting packages used in the code chunks below.
library(lattice)
library(colorRamps)
We load some GTEx summary statistics, as well as some of the results generated from the mash analysis of the GTEx data.
covmat <- readRDS(paste("../output/MatrixEQTLSumStats.Portable.Z.coved.K3.P3",
"lite.single.expanded.rds",sep = "."))
pis <- readRDS(paste("../output/MatrixEQTLSumStats.Portable.Z.coved.K3.P3",
"lite.single.expanded.V1.pihat.rds",sep = "."))$pihat
z.stat <- readRDS("../data/MatrixEQTLSumStats.Portable.Z.rds")$strong.z
pi.mat <- matrix(pis[-length(pis)],ncol = 54,nrow = 22,byrow = TRUE)
names <- colnames(z.stat)
colnames(pi.mat) <-
c("ID","X'X","SVD","F1","F2","F3","F4","F5","SFA_Rank5",names,"ALL")
Compute the correlations from the \(k=3\) covariance matrix.
k <- 3
x <- cov2cor(covmat[[k]])
x[x < 0] <- 0
Next, we load the tissue indices and tissue names:
colnames(x) <- names
rownames(x) <- names
h <- read.table("../data/uk3rowindices.txt")[,1]
For the plots of the eigenvectors, we load the colours that are conventionally used to represent the tissues in plots.
missing.tissues <- c(7,8,19,20,24,25,31,34,37)
color.gtex <- read.table("../data/GTExColors.txt",sep = "\t",
comment.char = '')[-missing.tissues,]
The posterior mixture weights give the relative importance of the covariance matrices for capturing patterns in the data.
barplot(colSums(pi.mat),las = 2,cex.names = 0.5)
Version | Author | Date |
---|---|---|
f01cfd4 | Peter Carbonetto | 2018-06-05 |
Here we see that the SVD component has the largest weight.
Now we produce the heatmap showing the full covariance matrix.
smat <- (x[(h),(h)])
smat[lower.tri(smat)] <- NA
clrs <- colorRampPalette(rev(c("#D73027","#FC8D59","#FEE090","#FFFFBF",
"#E0F3F8","#91BFDB","#4575B4")))(64)
lat <- x[rev(h),rev(h)]
lat[lower.tri(lat)] <- NA
n <- nrow(lat)
print(levelplot(lat[n:1,],col.regions = clrs,xlab = "",ylab = "",
colorkey = TRUE,at = seq(0,1,length.out = 64),
scales = list(cex = 0.6,x = list(rot = 45))))
Version | Author | Date |
---|---|---|
f01cfd4 | Peter Carbonetto | 2018-06-05 |
The eigenvectors capture the predominant patterns in the Uk3 covariance matrix.
k <- 3
vold <- svd(covmat[[k]])$v
u <- svd(covmat[[k]])$u
d <- svd(covmat[[k]])$d
v <- vold[h,] # Shuffle so correct order
names <- names[h]
color.gtex <- color.gtex[h,]
for (j in 1:3)
barplot(v[,j]/v[,j][which.max(abs(v[,j]))],names = "",cex.names = 0.5,
las = 2,main = paste0("EigenVector",j,"Uk",k),
col = as.character(color.gtex[,2]))
Version | Author | Date |
---|---|---|
f01cfd4 | Peter Carbonetto | 2018-06-05 |
Version | Author | Date |
---|---|---|
f01cfd4 | Peter Carbonetto | 2018-06-05 |
Version | Author | Date |
---|---|---|
f01cfd4 | Peter Carbonetto | 2018-06-05 |
The first eigenvector reflects broad sharing among tissues, with all effects in the same direction; the second eigenvector captures differences between brain (and, to a less extent, testis and pituitary) vs other tissues; the third eigenvector primarily captures effects that are stronger in whole blood than elsewhere.
sessionInfo()
# R version 3.4.3 (2017-11-30)
# Platform: x86_64-apple-darwin15.6.0 (64-bit)
# Running under: macOS High Sierra 10.13.5
#
# 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] colorRamps_2.3 lattice_0.20-35
#
# loaded via a namespace (and not attached):
# [1] workflowr_1.0.1.9000 Rcpp_0.12.17 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
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