Last updated: 2020-02-02
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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
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Modified: analysis/nucSpecinEQTLs.Rmd
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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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File | Version | Author | Date | Message |
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Rmd | fda9908 | brimittleman | 2020-02-02 | add RBP res |
library(workflowr)
This is workflowr version 1.5.0
Run ?workflowr for help getting started
library(tidyverse)
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I will use eClip data from encode to study RNA binding. I will use the results from K562 cells. They do not have data for LCLs.
Downloading the bed files for 25 different proteins.
mkdir ../data/eCLip/
I will search in all of the gene UTRs for each of these. I will see if there is more likely to be an overlap in genes with APA.
I need to cut the CHR from each file.
for i in $(ls ../data/eCLip/*.bed)
do
name=$(echo ${i} | cut -f 4 -d '/' | cut -f 1 -d '.')
sed 's/^chr//' $i > ../data/eCLip/${name}.noCHR.bed
done
Run overlap for all othese with bedtools. I will make a bedfile with the longest UTR annoation for each gene.
UTR=read.table("../../genome_anotation_data/RefSeq_annotations/ncbiRefSeq_UTR3.sort.bed",col.names = c('chr','start','end','utr','gene', 'score','strand'),stringsAsFactors = F) %>%
mutate(UTRlength=end-start) %>%
group_by(gene)%>%
arrange(desc(UTRlength)) %>%
filter(row_number() == 1L) %>%
select(chr, start,end, gene, score, strand)
write.table(UTR, "../data/eCLip/UTRregions.bed", row.names = F, col.names = F, quote = F,sep="\t")
sort -k1,1 -k2,2n ../data/eCLip/UTRregions.bed > ../data/eCLip/UTRregions.sort.bed
Merge the regions with the name being the name of the RNA.
cat ../data/eCLip/*.noCHR.bed > ../data/eCLip/ALLRBP.noCHR.bed
sort -k1,1 -k2,2n ../data/eCLip/ALLRBP.noCHR.bed | cut -f 1-6 > ../data/eCLip/ALLRBP.noCHR.sort.bed
cat: ../data/eCLip/ALLRBP.noCHR.bed: input file is output file
Now I can map.Print the distinct RBP in each UTR.
bedtools map -a ../data/eCLip/UTRregions.sort.bed -b ../data/eCLip/ALLRBP.noCHR.sort.bed -c 4 -o distinct -s > ../data/eCLip/AllUTRsMappedallRBP.txt
I will also run this all seperatly for downstream analysis:
sbatch MapAllRBP.sh
I will compare genes with and without QTLs.
QTL_genes=read.table("../data/apaQTLs/NuclearapaQTLGenes.txt",col.names = "gene",stringsAsFactors = F)
QTLTested_genes=read.table("../data/apaQTLs/TestedNuclearapaQTLGenes.txt",col.names = "gene",stringsAsFactors = F) %>% mutate(QTL=ifelse(gene %in% QTL_genes$gene, "Yes","No"))
PHF6=read.table("../data/eCLip/UTRregions_ENCFF016IHL_PHF6.txt",header=F, col.names = c('chr','start','end','gene','score','strand','RBP'),stringsAsFactors = F) %>% inner_join(QTLTested_genes, by='gene') %>% mutate(PHF6=ifelse(RBP=="PHF6_K562_rep01", "Yes","No"))
x=nrow(PHF6 %>% filter(PHF6=="Yes", QTL=="Yes"))
m= nrow(PHF6 %>% filter(PHF6=="Yes"))
n=nrow(PHF6 %>% filter(PHF6!="Yes"))
k=nrow(PHF6 %>% filter(QTL=="Yes"))
#expected
which(grepl(max(dhyper(1:x, m, n, k)), dhyper(1:x, m, n, k)))
[1] 77
#actual:
x
[1] 77
#pval
phyper(x,m,n,k,lower.tail=F)
[1] 0.8531311
Test for any RBP:
All=read.table("../data/eCLip/AllUTRsMappedallRBP.txt",header=F, col.names = c('chr','start','end','gene','score','strand','RBP'),stringsAsFactors = F) %>%
inner_join(QTLTested_genes, by='gene') %>%
mutate(HasRBP=ifelse(RBP!=".", "Yes","No"))
x=nrow(All %>% filter(HasRBP=="Yes", QTL=="Yes"))
m= nrow(All %>% filter(HasRBP=="Yes"))
n=nrow(All %>% filter(HasRBP!="Yes"))
k=nrow(All %>% filter(QTL=="Yes"))
#expected
which(grepl(max(dhyper(1:x, m, n, k)), dhyper(1:x, m, n, k)))
[1] 403
#actual:
x
[1] 429
#pval
phyper(x,m,n,k,lower.tail=F)
[1] 0.007323885
This means genes with QTLs are enriched for genes with an identified RBP in the its UTR.
Let’s look at this by the location of QTL.
QTL_intron=read.table("../data/apaQTLs/Nuclear_apaQTLs4pc_5fdr.bed",stringsAsFactors = F,header = T) %>%
separate(name, into=c("gene", "PAS","loc"),sep=":") %>%
filter(loc=="intron")
QTL_UTR=read.table("../data/apaQTLs/Nuclear_apaQTLs4pc_5fdr.bed",stringsAsFactors = F,header = T) %>%
separate(name, into=c("gene", "PAS","loc"),sep=":") %>%
filter(loc=="utr3")
QTLTested_intron=read.table("../data/apaQTLs/TestedNuclearapaQTLGenes.txt",col.names = "gene",stringsAsFactors = F) %>% mutate(QTL=ifelse(gene %in% QTL_intron$gene, "Yes","No"))
QTLTested_utr=read.table("../data/apaQTLs/TestedNuclearapaQTLGenes.txt",col.names = "gene",stringsAsFactors = F) %>% mutate(QTL=ifelse(gene %in% QTL_UTR$gene, "Yes","No"))
All_intron=read.table("../data/eCLip/AllUTRsMappedallRBP.txt",header=F, col.names = c('chr','start','end','gene','score','strand','RBP'),stringsAsFactors = F) %>%
inner_join(QTLTested_intron, by='gene') %>%
mutate(HasRBP=ifelse(RBP!=".", "Yes","No"))
x=nrow(All_intron %>% filter(HasRBP=="Yes", QTL=="Yes"))
m= nrow(All_intron %>% filter(HasRBP=="Yes"))
n=nrow(All_intron %>% filter(HasRBP!="Yes"))
k=nrow(All_intron %>% filter(QTL=="Yes"))
#expected
which(grepl(max(dhyper(1:x, m, n, k)), dhyper(1:x, m, n, k)))
[1] 110
#actual:
x
[1] 110
#pval
phyper(x,m,n,k,lower.tail=F)
[1] 0.8893598
All_UTR=read.table("../data/eCLip/AllUTRsMappedallRBP.txt",header=F, col.names = c('chr','start','end','gene','score','strand','RBP'),stringsAsFactors = F) %>%
inner_join(QTLTested_utr, by='gene') %>%
mutate(HasRBP=ifelse(RBP!=".", "Yes","No"))
x=nrow(All_UTR %>% filter(HasRBP=="Yes", QTL=="Yes"))
m= nrow(All_UTR %>% filter(HasRBP=="Yes"))
n=nrow(All_UTR %>% filter(HasRBP!="Yes"))
k=nrow(All_UTR %>% filter(QTL=="Yes"))
#expected
which(grepl(max(dhyper(1:x, m, n, k)), dhyper(1:x, m, n, k)))
[1] 182
#actual:
x
[1] 201
#pval
phyper(x,m,n,k,lower.tail=F)
[1] 0.003616523
This is only significant for genes with QTL’s associated with the 3’ UTR.
Try to find which RBP is driving the assocations.
I want a function that will go through each of the RBPs and test for this enrichment association.
for i in $(ls ../data/eCLip/ENCFF*.small.noCHR.bed)
do
name=$(echo ${i} | cut -f 4 -d '/' | cut -f 1 -d '.')
echo $name >> ../data/eCLip/RBPtested.txt
done
RBP_names=read.table("../data/eCLip/RBPtested.txt", col.names = "RBP",stringsAsFactors = F)
expected=c()
actual=c()
pval=c()
for (RBP in RBP_names$RBP){
RBPfile=read.table(paste("../data/eCLip/UTRregions_", RBP,".txt", sep=""),header=F, col.names = c('chr','start','end','gene','score','strand','RBP'), stringsAsFactors = F) %>%
inner_join(QTLTested_genes, by='gene') %>%
mutate(HasRBP=ifelse(RBP!=".", "Yes","No"))
x=nrow(RBPfile %>% filter(HasRBP=="Yes", QTL=="Yes"))
m= nrow(RBPfile %>% filter(HasRBP=="Yes"))
n=nrow(RBPfile %>% filter(HasRBP!="Yes"))
k=nrow(RBPfile %>% filter(QTL=="Yes"))
expected=c(expected, which(grepl(max(dhyper(1:x, m, n, k)), dhyper(1:x, m, n, k))))
actual=c(actual,x)
pval=c(pval,phyper(x,m,n,k,lower.tail=F))
}
RBP_names_res= as.data.frame(cbind(RBP=RBP_names$RBP, expected,actual,pval)) %>% separate(RBP, into=c("exp", "protein"),sep="_")
RBP_names_res$pval=as.numeric(as.character(RBP_names_res$pval))
ggplot(RBP_names_res, aes(x=protein, y=-log10(pval),fill=protein))+geom_bar(stat="identity") +theme(legend.position = "none", axis.text.x = element_text(angle = 90)) +labs(title="Enrichment for nuclear apaQTL genes with RBP in UTR",y="-log10(Enrichment pval)") + geom_hline(yintercept = 2)
Do this for UTR QTL
expectedUTR=c()
actualUTR=c()
pvalUTR=c()
for (RBP in RBP_names$RBP){
RBPfile=read.table(paste("../data/eCLip/UTRregions_", RBP,".txt", sep=""),header=F, col.names = c('chr','start','end','gene','score','strand','RBP'), stringsAsFactors = F) %>%
inner_join(QTLTested_utr, by='gene') %>%
mutate(HasRBP=ifelse(RBP!=".", "Yes","No"))
x=nrow(RBPfile %>% filter(HasRBP=="Yes", QTL=="Yes"))
m= nrow(RBPfile %>% filter(HasRBP=="Yes"))
n=nrow(RBPfile %>% filter(HasRBP!="Yes"))
k=nrow(RBPfile %>% filter(QTL=="Yes"))
expectedUTR=c(expectedUTR, which(grepl(max(dhyper(1:x, m, n, k)), dhyper(1:x, m, n, k))))
actualUTR=c(actualUTR,x)
pvalUTR=c(pvalUTR,phyper(x,m,n,k,lower.tail=F))
}
RBP_names_resUTR= as.data.frame(cbind(RBP=RBP_names$RBP, expectedUTR,actualUTR,pvalUTR)) %>% separate(RBP, into=c("exp", "protein"),sep="_")
RBP_names_resUTR$pvalUTR=as.numeric(as.character(RBP_names_resUTR$pvalUTR))
ggplot(RBP_names_resUTR, aes(x=protein, y=-log10(pvalUTR),fill=protein))+geom_bar(stat="identity") +theme(legend.position = "none", axis.text.x = element_text(angle = 90)) +labs(title="Enrichment for 3' UTR nuclear apaQTL genes with RBP in UTR",y="-log10(Enrichment pval)") + geom_hline(yintercept = 2)
Intronic:
expectedIntron=c()
actualIntron=c()
pvalIntron=c()
for (RBP in RBP_names$RBP){
RBPfile=read.table(paste("../data/eCLip/UTRregions_", RBP,".txt", sep=""),header=F, col.names = c('chr','start','end','gene','score','strand','RBP'), stringsAsFactors = F) %>%
inner_join(QTLTested_intron, by='gene') %>%
mutate(HasRBP=ifelse(RBP!=".", "Yes","No"))
x=nrow(RBPfile %>% filter(HasRBP=="Yes", QTL=="Yes"))
m= nrow(RBPfile %>% filter(HasRBP=="Yes"))
n=nrow(RBPfile %>% filter(HasRBP!="Yes"))
k=nrow(RBPfile %>% filter(QTL=="Yes"))
expectedIntron=c(expectedIntron, which(grepl(max(dhyper(1:x, m, n, k)), dhyper(1:x, m, n, k))))
actualIntron=c(actualIntron,x)
pvalIntron=c(pvalIntron,phyper(x,m,n,k,lower.tail=F))
}
RBP_names_resIntron= as.data.frame(cbind(RBP=RBP_names$RBP, expectedIntron,actualIntron,pvalIntron)) %>% separate(RBP, into=c("exp", "protein"),sep="_")
RBP_names_resIntron$pvalIntron=as.numeric(as.character(RBP_names_resIntron$pvalIntron))
ggplot(RBP_names_resIntron, aes(x=protein, y=-log10(pvalIntron),fill=protein))+geom_bar(stat="identity") +theme(legend.position = "none", axis.text.x = element_text(angle = 90)) +labs(title="Enrichment for Intronic nuclear apaQTL genes with RBP in UTR",y="-log10(Enrichment pval)") + geom_hline(yintercept = 2)
Looks like the protiens driving this are SAFB and FUS.
FUS: Associated both with RNA splicing and nuclear export.
SAFB: cotranscriptional.
Compare to total apaQTLs:
TotalQTL_genes=read.table("../data/apaQTLs/TotalapaQTLGenes.txt",col.names = "gene",stringsAsFactors = F)
TotalQTLTested_genes=read.table("../data/apaQTLs/TestedTotalapaQTLGenes.txt",col.names = "gene",stringsAsFactors = F) %>% mutate(QTL=ifelse(gene %in% QTL_genes$gene, "Yes","No"))
expectedT=c()
actualT=c()
pvalT=c()
for (RBP in RBP_names$RBP){
RBPfile=read.table(paste("../data/eCLip/UTRregions_", RBP,".txt", sep=""),header=F, col.names = c('chr','start','end','gene','score','strand','RBP'), stringsAsFactors = F) %>%
inner_join(TotalQTLTested_genes, by='gene') %>%
mutate(HasRBP=ifelse(RBP!=".", "Yes","No"))
x=nrow(RBPfile %>% filter(HasRBP=="Yes", QTL=="Yes"))
m= nrow(RBPfile %>% filter(HasRBP=="Yes"))
n=nrow(RBPfile %>% filter(HasRBP!="Yes"))
k=nrow(RBPfile %>% filter(QTL=="Yes"))
expectedT=c(expectedT, which(grepl(max(dhyper(1:x, m, n, k)), dhyper(1:x, m, n, k))))
actualT=c(actualT,x)
pvalT=c(pvalT,phyper(x,m,n,k,lower.tail=F))
}
RBP_names_resT= as.data.frame(cbind(RBP=RBP_names$RBP, expectedT,actualT,pvalT)) %>% separate(RBP, into=c("exp", "protein"),sep="_")
RBP_names_resT$pvalT=as.numeric(as.character(RBP_names_resT$pvalT))
ggplot(RBP_names_resT, aes(x=protein, y=-log10(pvalT),fill=protein))+geom_bar(stat="identity") +theme(legend.position = "none", axis.text.x = element_text(angle = 90)) +labs(title="Enrichment for total apaQTL genes with RBP in UTR",y="-log10(Enrichment pval)") + geom_hline(yintercept = 2)
Total fraction GRWD1 and HNRNPC pop up too
GRWD1: encoded protein may play a critical role in ribosome biogenesis and may also play a role in histone methylation through interactions
HNRNPC: The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport
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 workflowr_1.5.0
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 tools_3.5.1
[9] digest_0.6.18 lubridate_1.7.4 jsonlite_1.6 evaluate_0.12
[13] nlme_3.1-137 gtable_0.2.0 lattice_0.20-38 pkgconfig_2.0.2
[17] rlang_0.4.0 cli_1.1.0 rstudioapi_0.10 yaml_2.2.0
[21] haven_1.1.2 withr_2.1.2 xml2_1.2.0 httr_1.3.1
[25] knitr_1.20 hms_0.4.2 generics_0.0.2 fs_1.3.1
[29] rprojroot_1.3-2 grid_3.5.1 tidyselect_0.2.5 glue_1.3.0
[33] R6_2.3.0 readxl_1.1.0 rmarkdown_1.10 modelr_0.1.2
[37] magrittr_1.5 whisker_0.3-2 backports_1.1.2 scales_1.0.0
[41] promises_1.0.1 htmltools_0.3.6 rvest_0.3.2 assertthat_0.2.0
[45] colorspace_1.3-2 httpuv_1.4.5 labeling_0.3 stringi_1.2.4
[49] lazyeval_0.2.1 munsell_0.5.0 broom_0.5.1 crayon_1.3.4