Last updated: 2020-01-31
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Knit directory: apaQTL/analysis/
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Unstaged changes:
Modified: analysis/LDregress.Rmd
Modified: analysis/NuclearSpecIncludeNotTested.Rmd
Modified: analysis/PASdescriptiveplots.Rmd
Modified: analysis/Readdistagainstfeatures.Rmd
Modified: analysis/nucSpecinEQTLs.Rmd
Modified: analysis/overlapapaqtlsandeqtls.Rmd
Modified: analysis/pQTLexampleplot.Rmd
Modified: analysis/propeQTLs_explained.Rmd
Modified: analysis/version15bpfilter.Rmd
Modified: code/DistPAS2Sig.py
Modified: code/apaQTLsnake.err
Deleted: code/test.txt
Deleted: reads_graphs.Rmd
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Rmd | 3a8156f | brimittleman | 2020-01-31 | wflow_publish(c(“analysis/index.Rmd”, “analysis/ConservationPAS.Rmd”)) |
In this analysis I want to study the conservation of the PAS. I will compare PAS with QTLs and those without. I will use PhyloP score. PhyloP scores for 100 vertibrates are available on the genome browser.
library(workflowr)
This is workflowr version 1.5.0
Run ?workflowr for help getting started
library(tidyverse)
── Attaching packages ────────────────────────────────────────────────────────────── tidyverse 1.2.1 ──
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✔ tidyr 0.8.3 ✔ stringr 1.3.1
✔ readr 1.3.1 ✔ forcats 0.3.0
── Conflicts ───────────────────────────────────────────────────────────────── tidyverse_conflicts() ──
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library(ggpubr)
Loading required package: magrittr
Attaching package: 'magrittr'
The following object is masked from 'package:purrr':
set_names
The following object is masked from 'package:tidyr':
extract
mkdir ../data/phylop/
PhyloP: Column #1 contains a one-based position coordinate. Column #2 contains a score showing the posterior probability that the phylogenetic hidden Markov model (HMM) of phastCons is in its most conserved state at that base position. I will use pybigwig to extract the regions I care about.
I will look at the 200 basepairs around each PAS.
pas=read.table("../data/PAS/APAPAS_GeneLocAnno.5perc.sort.bed",col.names = c("chr","start","end","name","score","strand")) %>% mutate(newStart=end-100,newEnd=end+100) %>% select(chr,newStart,newEnd, name)
write.table(pas,"../data/phylop/PAS_regions.txt",col.names = F,row.names = F,quote = F,sep="\t")
python extractPACmeanPhyloP.py
Add information about qtl or not:
nucQTL=read.table("../data/apaQTLs/Nuclear_apaQTLs4pc_5fdr.txt",header = T)
phylores=read.table("../data/phylop/PAS_phyloP.txt", col.names = c("chr","start","end","name", "phyloP"), stringsAsFactors = F) %>% drop_na() %>% separate(name,into=c("pasnum","geneid"), sep=":") %>% mutate(PAS=paste("peak",pasnum,sep="")) %>% mutate(HasQTL=ifelse(PAS %in% nucQTL$Peak, "Yes","No"))
41,810 - 41649
lost 161 to NAs
Plot:
ggplot(phylores,aes(x=phyloP, by=HasQTL, fill=HasQTL)) +geom_density(alpha=.5)
ggplot(phylores,aes(y=phyloP, x=HasQTL,fill=HasQTL)) + geom_boxplot() + stat_compare_means()+ scale_fill_brewer(palette = "Dark2", name="Signficant")
With a QTL is lower score. Look at enrichment for negative
x=nrow(phylores %>% filter(HasQTL=="Yes", phyloP<0))
m= nrow(phylores %>% filter(phyloP<0))
n=nrow(phylores %>% filter(phyloP>=0))
k=nrow(phylores %>% filter(HasQTL=="Yes"))
#expected
which(grepl(max(dhyper(1:x, m, n, k)), dhyper(1:x, m, n, k)))
[1] 140
#actual:
x
[1] 196
#pval
phyper(x,m,n,k,lower.tail=F)
[1] 8.44718e-08
Enriched for regions expected to be rapidly evolving.
Try with smaller regions:
pas100=read.table("../data/PAS/APAPAS_GeneLocAnno.5perc.sort.bed",col.names = c("chr","start","end","name","score","strand")) %>% mutate(newStart=end-50,newEnd=end+50) %>% select(chr,newStart,newEnd, name)
write.table(pas,"../data/phylop/PAS100_regions.txt",col.names = F,row.names = F,quote = F,sep="\t")
python extactPAS100meanphyloP.py
phylores100=read.table("../data/phylop/PAS100_phyloP.txt", col.names = c("chr","start","end","name", "phyloP"), stringsAsFactors = F) %>% drop_na() %>% separate(name,into=c("pasnum","geneid"), sep=":") %>% mutate(PAS=paste("peak",pasnum,sep="")) %>% mutate(HasQTL=ifelse(PAS %in% nucQTL$Peak, "Yes","No"))
ggplot(phylores100,aes(x=phyloP, by=HasQTL, fill=HasQTL)) +geom_density(alpha=.5)
ggplot(phylores100,aes(y=phyloP, x=HasQTL,fill=HasQTL)) + geom_boxplot() + stat_compare_means()+ scale_fill_brewer(palette = "Dark2", name="Signficant")
x=nrow(phylores100 %>% filter(HasQTL=="Yes", phyloP<0))
m= nrow(phylores100 %>% filter(phyloP<0))
n=nrow(phylores100 %>% filter(phyloP>=0))
k=nrow(phylores100 %>% filter(HasQTL=="Yes"))
#expected
which(grepl(max(dhyper(1:x, m, n, k)), dhyper(1:x, m, n, k)))
[1] 140
#actual:
x
[1] 196
#pval
phyper(x,m,n,k,lower.tail=F)
[1] 8.44718e-08
Exact same results.
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] ggpubr_0.2 magrittr_1.5 forcats_0.3.0 stringr_1.3.1
[5] dplyr_0.8.0.1 purrr_0.3.2 readr_1.3.1 tidyr_0.8.3
[9] tibble_2.1.1 ggplot2_3.1.1 tidyverse_1.2.1 workflowr_1.5.0
loaded via a namespace (and not attached):
[1] tidyselect_0.2.5 haven_1.1.2 lattice_0.20-38
[4] colorspace_1.3-2 generics_0.0.2 htmltools_0.3.6
[7] yaml_2.2.0 rlang_0.4.0 later_0.7.5
[10] pillar_1.3.1 glue_1.3.0 withr_2.1.2
[13] RColorBrewer_1.1-2 modelr_0.1.2 readxl_1.1.0
[16] plyr_1.8.4 munsell_0.5.0 gtable_0.2.0
[19] cellranger_1.1.0 rvest_0.3.2 evaluate_0.12
[22] labeling_0.3 knitr_1.20 httpuv_1.4.5
[25] broom_0.5.1 Rcpp_1.0.2 promises_1.0.1
[28] scales_1.0.0 backports_1.1.2 jsonlite_1.6
[31] fs_1.3.1 hms_0.4.2 digest_0.6.18
[34] stringi_1.2.4 grid_3.5.1 rprojroot_1.3-2
[37] cli_1.1.0 tools_3.5.1 lazyeval_0.2.1
[40] crayon_1.3.4 whisker_0.3-2 pkgconfig_2.0.2
[43] xml2_1.2.0 lubridate_1.7.4 assertthat_0.2.0
[46] rmarkdown_1.10 httr_1.3.1 rstudioapi_0.10
[49] R6_2.3.0 nlme_3.1-137 git2r_0.26.1
[52] compiler_3.5.1