Last updated: 2020-03-10
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Knit directory: apaQTL/analysis/
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Unstaged changes:
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Rmd | 6719a59 | brimittleman | 2020-03-10 | add mixed plot |
html | 71f66d2 | brimittleman | 2020-02-28 | Build site. |
Rmd | e5dbb2f | brimittleman | 2020-02-28 | add all lines in 1 |
html | f19db64 | brimittleman | 2020-02-28 | Build site. |
Rmd | 2969449 | brimittleman | 2020-02-28 | add all lines in 1 |
html | 11ea802 | brimittleman | 2020-02-27 | Build site. |
Rmd | 7449f09 | brimittleman | 2020-02-27 | add figure spec |
html | 1ca62a2 | brimittleman | 2020-02-20 | Build site. |
Rmd | 662a604 | brimittleman | 2020-02-20 | add riboqq and PM coloc |
In the paper I have qqPlots where I took the apaQTL data and subset it by QTL sets. I never did this for riboQTLs. I will get the riboQTLs from Battle et al and remake the plot including these.
library(tidyverse)
── Attaching packages ────────────────────────────────────────────────────────────────── tidyverse 1.2.1 ──
✔ ggplot2 3.1.1 ✔ purrr 0.3.2
✔ tibble 2.1.1 ✔ dplyr 0.8.0.1
✔ tidyr 0.8.3 ✔ stringr 1.3.1
✔ readr 1.3.1 ✔ forcats 0.3.0
── Conflicts ───────────────────────────────────────────────────────────────────── tidyverse_conflicts() ──
✖ dplyr::filter() masks stats::filter()
✖ dplyr::lag() masks stats::lag()
geneNames=read.table("../../genome_anotation_data/ensemble_to_genename.txt", sep="\t", col.names = c('ENSG', 'GeneName', 'source' ),stringsAsFactors = F, header = T)
riboRes=read.table("../data/Battle_pQTL/riboQTLs_battle.txt", header = T,stringsAsFactors = F) %>% inner_join(geneNames,by="ENSG")
exPe=read.table("../data/Li_eQTLs/explainedEgenes.txt", col.names = "GeneName")
UexPe=read.table("../data/Li_eQTLs/UnexplainedEgenes.txt",col.names = "GeneName")
allE=exPe %>% full_join(UexPe,by="GeneName")
Warning: Column `GeneName` joining factors with different levels, coercing
to character vector
riboRes$bh=p.adjust(riboRes$perm.p.values, method="fdr")
riboRes_sig= riboRes %>% filter(-log10(bh)>=1)
riboGenes=riboRes_sig %>% select(GeneName) %>% anti_join(allE)
Joining, by = "GeneName"
write.table(riboGenes, file="../data/Battle_pQTL/RiboQTLGeneNames.txt", row.names = F, col.names = F, quote = F, sep="\t")
mkdir ../data/ApaByRgene
python subsetpermAPAwithGenelist.py ../data/Battle_pQTL/RiboQTLGeneNames.txt Nuclear ../data/ApaByRgene/NuclearApaRGenes.txt
python subsetpermAPAwithGenelist.py ../data/Battle_pQTL/RiboQTLGeneNames.txt Total ../data/ApaByRgene/TotalApaRGenes.txt
python subsetAPAnotEorR.py Nuclear ../data/ApaByRgene/NotRorE_nuclear.txt
python subsetAPAnotEorR.py Total ../data/ApaByRgene/NotRorE_total.txt
tot.notEorR=read.table("../data/ApaByRgene/NotRorE_total.txt",stringsAsFactors = F,col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval"))
tot.RS=read.table("../data/ApaByRgene/TotalApaRGenes.txt",stringsAsFactors = F,col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval"))
tot.ES=read.table("../data/ApaByPgene/TotalApaESGenes.txt",stringsAsFactors = F, col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval") )
tot.ex=read.table("../data/ApaByEgene/TotalApaexplainedeGenes.txt",stringsAsFactors = F,col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval"))
tot.un=read.table("../data/ApaByEgene/TotalApaUnexplainedeGenes.txt",stringsAsFactors = F, col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval") )
tot_allE=as.data.frame(rbind(tot.ex,tot.un))
tot.RS=na.omit(tot.RS)
tot.notEorR=na.omit(tot.notEorR)
tot.ES=na.omit(tot.ES)
tot.un=na.omit(tot.un)
qqplot(-log10(runif(nrow(tot.notEorR))), -log10(tot.notEorR$bpval), xlab="-log10(Uniform)", ylab="-log10(beta pval)", main="Total Apa")
points(sort(-log10(runif(nrow(tot.RS)))), sort(-log10(tot.RS$bpval)),col= alpha("Red"))
points(sort(-log10(runif(nrow(tot_allE)))), sort(-log10(tot_allE$bpval)),col= alpha("blue"))
abline(0,1)
legend("topleft", legend=c("Neither eGenes nor rGenes", "rGenes", "eGenes"),col=c("black", "red","blue"), pch=16,bty = 'n')
Version | Author | Date |
---|---|---|
1ca62a2 | brimittleman | 2020-02-20 |
wilcox.test(tot.RS$bpval,tot.notEorR$bpval,alternative="less")
Wilcoxon rank sum test with continuity correction
data: tot.RS$bpval and tot.notEorR$bpval
W = 9336600, p-value = 0.0001811
alternative hypothesis: true location shift is less than 0
wilcox.test(tot_allE$bpval,tot.notEorR$bpval,alternative="less")
Wilcoxon rank sum test with continuity correction
data: tot_allE$bpval and tot.notEorR$bpval
W = 43090000, p-value = 1.878e-11
alternative hypothesis: true location shift is less than 0
wilcox.test(tot.RS$bpval,tot_allE$bpval,alternative="less")
Wilcoxon rank sum test with continuity correction
data: tot.RS$bpval and tot_allE$bpval
W = 1554300, p-value = 0.3891
alternative hypothesis: true location shift is less than 0
nuc.notEorR=read.table("../data/ApaByRgene/NotRorE_nuclear.txt",stringsAsFactors = F,col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval"))
nuc.RS=read.table("../data/ApaByRgene/NuclearApaRGenes.txt",stringsAsFactors = F,col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval"))
nuc.P=read.table("../data/ApaByPgene/NuclearApaPSGenes.txt",stringsAsFactors = F,col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval"))
nuc.ES=read.table("../data/ApaByPgene/NuclearApaESGenes.txt",stringsAsFactors = F, col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval") )
nuc.ex=read.table("../data/ApaByEgene/NuclearApaexplainedeGenes.txt",stringsAsFactors = F,col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval"))
nuc.un=read.table("../data/ApaByEgene/NuclearApaUnexplainedeGenes.txt",stringsAsFactors = F, col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval") )
nuc.un=na.omit(nuc.un)
nuc.RS=na.omit(nuc.RS)
#nuc.notERorP=na.omit(nuc.notERorP)
nuc.P=na.omit(nuc.P)
nuc.notEorR=na.omit(nuc.notEorR)
nuc.ES=na.omit(nuc.ES)
nuc_allE=as.data.frame(rbind(nuc.ex,nuc.un))
qqplot(-log10(runif(nrow(nuc.notEorR))), -log10(nuc.notEorR$bpval), xlab="-log10(Uniform)", ylab="-log10(beta pval)", main="Nuclear Apa")
points(sort(-log10(runif(nrow(nuc.RS)))), sort(-log10(nuc.RS$bpval)),col= alpha("Red"))
points(sort(-log10(runif(nrow(nuc_allE)))), sort(-log10(nuc_allE$bpval)),col= alpha("blue"))
abline(0,1)
legend("topleft", legend=c("Neither eGenes nor rGenes", "rGenes", "eGenes"),col=c("black", "red","blue","green"), pch=16,bty = 'n')
Version | Author | Date |
---|---|---|
1ca62a2 | brimittleman | 2020-02-20 |
wilcox.test(nuc.RS$bpval,nuc.notEorR$bpval,alternative="less")
Wilcoxon rank sum test with continuity correction
data: nuc.RS$bpval and nuc.notEorR$bpval
W = 13007000, p-value = 0.01029
alternative hypothesis: true location shift is less than 0
wilcox.test(nuc_allE$bpval,nuc.notEorR$bpval,alternative="less")
Wilcoxon rank sum test with continuity correction
data: nuc_allE$bpval and nuc.notEorR$bpval
W = 57056000, p-value = 6.194e-13
alternative hypothesis: true location shift is less than 0
wilcox.test(nuc.RS$bpval,nuc_allE$bpval,alternative="less")
Wilcoxon rank sum test with continuity correction
data: nuc.RS$bpval and nuc_allE$bpval
W = 2189300, p-value = 0.8658
alternative hypothesis: true location shift is less than 0
No QTL at all.
python subsetNootherQTL.py Nuclear ../data/ApaByRgene/NotANY_nuclear.txt
notany_nuc=read.table("../data/ApaByRgene/NotANY_nuclear.txt",stringsAsFactors = F, col.names = c("pid", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval") )
notany_nuc=na.omit(notany_nuc)
qqplot(-log10(runif(nrow(notany_nuc))), -log10(notany_nuc$bpval), xlab="-log10(Uniform)", ylab="-log10(beta pval)", main="Nuclear Apa")
points(sort(-log10(runif(nrow(nuc.RS)))), sort(-log10(nuc.RS$bpval)),col= alpha("Red"))
points(sort(-log10(runif(nrow(nuc.P)))), sort(-log10(nuc.P$bpval)),col= alpha("Blue"))
abline(0,1)
legend("topleft", legend=c("No Molecular QTL","rGenes", "pGenes"),col=c("black", "red","Blue"), pch=16,bty = 'n')
sessionInfo()
R version 3.5.1 (2018-07-02)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: Scientific Linux 7.4 (Nitrogen)
Matrix products: default
BLAS/LAPACK: /software/openblas-0.2.19-el7-x86_64/lib/libopenblas_haswellp-r0.2.19.so
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
[5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
[7] LC_PAPER=en_US.UTF-8 LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] forcats_0.3.0 stringr_1.3.1 dplyr_0.8.0.1 purrr_0.3.2
[5] readr_1.3.1 tidyr_0.8.3 tibble_2.1.1 ggplot2_3.1.1
[9] tidyverse_1.2.1
loaded via a namespace (and not attached):
[1] Rcpp_1.0.2 cellranger_1.1.0 plyr_1.8.4 compiler_3.5.1
[5] pillar_1.3.1 later_0.7.5 git2r_0.26.1 workflowr_1.6.0
[9] tools_3.5.1 digest_0.6.18 lubridate_1.7.4 jsonlite_1.6
[13] evaluate_0.12 nlme_3.1-137 gtable_0.2.0 lattice_0.20-38
[17] pkgconfig_2.0.2 rlang_0.4.0 cli_1.1.0 rstudioapi_0.10
[21] yaml_2.2.0 haven_1.1.2 withr_2.1.2 xml2_1.2.0
[25] httr_1.3.1 knitr_1.20 hms_0.4.2 generics_0.0.2
[29] fs_1.3.1 rprojroot_1.3-2 grid_3.5.1 tidyselect_0.2.5
[33] glue_1.3.0 R6_2.3.0 readxl_1.1.0 rmarkdown_1.10
[37] modelr_0.1.2 magrittr_1.5 whisker_0.3-2 backports_1.1.2
[41] scales_1.0.0 promises_1.0.1 htmltools_0.3.6 rvest_0.3.2
[45] assertthat_0.2.0 colorspace_1.3-2 httpuv_1.4.5 stringi_1.2.4
[49] lazyeval_0.2.1 munsell_0.5.0 broom_0.5.1 crayon_1.3.4