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File | Version | Author | Date | Message |
---|---|---|---|---|
html | d59b3c1 | Briana Mittleman | 2018-10-24 | Build site. |
Rmd | d8c6f3c | Briana Mittleman | 2018-10-24 | add ven diagrams |
Rmd | 70a8d68 | Briana Mittleman | 2018-10-23 | add anova pvalue to examples |
html | 5649809 | Briana Mittleman | 2018-10-22 | Build site. |
Rmd | c8dbaf0 | Briana Mittleman | 2018-10-22 | add apa prot rna overlap |
I want to use this analysis to look at the genes with a APAQTL and a protein QTL. I am trying to understand how many of these are independent of RNA.
I will first look at genes with significant QTLs in both phenotypes. I can use the pipeline I created in https://brimittleman.github.io/threeprimeseq/swarmPlots_QTLs.html to vizualize these snps.
library(workflowr)
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library(tidyverse)
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Gene Names:
geneNames=read.table("../data/ensemble_to_genename.txt", stringsAsFactors = F, header = T, sep="\t")
Significant APA QTLS:
nuclearAPA=read.table("../data/perm_QTL_trans/filtered_APApeaks_merged_allchrom_refseqGenes_pheno_Nuclear_transcript_permResBH.txt", stringsAsFactors = F, header = T) %>% separate(pid, into=c("chr", "start", "end", "id"), sep=":") %>% separate(id, into=c("Gene.name", "strand", "peaknum"), sep="_") %>% dplyr::filter(-log10(bh)>1)
totalAPA=read.table("../data/perm_QTL_trans/filtered_APApeaks_merged_allchrom_refseqGenes_pheno_Total_transcript_permResBH.txt", stringsAsFactors = F, header=T) %>% separate(pid, into=c("chr", "start", "end", "id"), sep=":") %>% separate(id, into=c("Gene.name", "strand", "peaknum"), sep="_") %>% dplyr::filter(-log10(bh)>1)
Significant Protien QTLs
protQTL=read.table("../data/other_qtls/fastqtl_qqnorm_prot.fixed.perm.out", col.names = c("Gene.stable.ID", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval"),stringsAsFactors=F) %>% inner_join(geneNames, by="Gene.stable.ID") %>% dplyr::select("Gene.name", "nvar", "shape1", "shape2", "dummy", "sid", "dist", "npval", "slope", "ppval", "bpval")
protQTL$bh=p.adjust(protQTL$bpval, method="fdr")
protQTL_sig= protQTL %>% dplyr::filter(-log10(bh)>1)
Overlap the QTLs by gene name:
genesBothTot=protQTL_sig %>% inner_join(totalAPA, by=c("Gene.name"))
genesBotNuc=protQTL_sig %>% inner_join(nuclearAPA, by=c("Gene.name"))
These are the genes that have a significant QTL in both.They are not the same snp. This may be because I am using the permuted snps. I will use the APA snp to make the plot.
plotQTL_func= function(SNP, peak, gene){
apaN_file=read.table(paste("../data/apaExamp/qtlSNP_PeakAPANuclear.", SNP, peak, ".txt", sep = "" ), header=T)
apaT_file=read.table(paste("../data/apaExamp/qtlSNP_PeakAPATotal.", SNP, peak, ".txt", sep = "" ), header=T)
su30_file=read.table(paste("../data/apaExamp/qtlSNP_Peak_4su_30_", SNP, gene, ".txt", sep=""), header = T)
su60_file=read.table(paste("../data/apaExamp/qtlSNP_Peak_4su_60_", SNP, gene, ".txt", sep=""), header=T)
RNA_file=read.table(paste("../data/apaExamp/qtlSNP_Peak_RNAseq_", SNP, gene, ".txt", sep=""),header=T)
RNAg_file=read.table(paste("../data/apaExamp/qtlSNP_Peak_RNAseqGeuvadis_", SNP, gene, ".txt", sep=""), header = T)
ribo_file=read.table(paste("../data/apaExamp/qtlSNP_Peak_ribo_", SNP, gene, ".txt", sep=""),header=T)
prot_file=read.table(paste("../data/apaExamp/qtlSNP_Peak_prot.", SNP, gene, ".txt", sep=""), header=T)
ggplot_func= function(file, molPhen,GENE,allOverlap_T){
file = file %>% mutate(genotype=Allele1 + Allele2)
file$genotype= as.factor(as.character(file$genotype))
plot=ggplot(file, aes(y=Pheno, x=genotype, by=genotype, fill=genotype)) + geom_boxplot(width=.25) + geom_jitter() + labs(y="Phenotpye",title=paste(molPhen, GENE, sep=": ")) + scale_fill_brewer(palette="Paired") + stat_compare_means(method = "anova", label.y.npc = "top")
return(plot)
}
apaNplot=ggplot_func(apaN_file, "Apa Nuclear", gene)
apaTplot=ggplot_func(apaT_file, "Apa Total", gene)
su30plot=ggplot_func(su30_file, "4su30",gene)
su60plot=ggplot_func(su60_file, "4su60",gene)
RNAplot=ggplot_func(RNA_file, "RNA",gene)
RNAgPlot=ggplot_func(RNAg_file, "RNAg",gene)
riboPlot= ggplot_func(ribo_file, "Ribo",gene)
protplot=ggplot_func(prot_file, "Protein",gene)
full_plot= plot_grid(apaNplot,apaTplot, RNAplot, protplot,nrow=2)
return (full_plot)
}
Total:
grep MRPL43 /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000055950
python createQTLsnpAPAPhenTable.py 10 10:102740271 peak44585 Total
python createQTLsnpAPAPhenTable.py 10 10:102740271 peak44585 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "10" "10:102740271" "ENSG00000055950"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*10:102740271* .
plotQTL_func(SNP="10:102740271", peak="peak44585", gene="ENSG00000055950")
Nuclear:
grep SWAP70 /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000133789
python createQTLsnpAPAPhenTable.py 11 11:9732917 peak49384 Total
python createQTLsnpAPAPhenTable.py 11 11:9732917 peak49384 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "11" "11:9732917" "ENSG00000133789"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*11:9732917* .
plotQTL_func(SNP="11:9732917", peak="peak49384", gene="ENSG00000133789")
grep DHRS7B /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000109016
python createQTLsnpAPAPhenTable.py 17 17:21102458 peak132739 Total
python createQTLsnpAPAPhenTable.py 17 17:21102458 peak132739 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "17" "17:21102458" "ENSG00000109016"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*17:21102458* .
plotQTL_func(SNP="17:21102458", peak="peak132739", gene="ENSG00000109016")
grep UBA6 /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000033178
python createQTLsnpAPAPhenTable.py 4 4:68502794 peak240167 Total
python createQTLsnpAPAPhenTable.py 4 4:68502794 peak240167 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "4" "4:68502794" "ENSG00000033178"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*4:68502794* .
plotQTL_func(SNP="4:68502794", peak="peak240167", gene="ENSG00000033178")
This is not the most effective way to do this because I am overlapping by gene then looking at the effect of the apaQTL snp. I want a method that will look directly at the effect of one snp. I can use the overlap files I created based on the APA qtls in other phenotypes. I can overlap the phenotypes and look for snps that have low pvalues in APA and protien.
I want the overlap where I started in APA qtls and found the snp in the mol file. I am starting with the total.
totAPAinsu30=read.table("../data/mol_overlap/APA2molTotal/TotAPAqtlsPval4su30.txt", header = T, stringsAsFactors = F)
totAPAinsu60=read.table("../data/mol_overlap/APA2molTotal/TotAPAqtlsPval4su60.txt", header = T, stringsAsFactors = F)
totAPAinRNA=read.table("../data/mol_overlap/APA2molTotal/TotAPAqtlsPvalRNA.txt", header = T, stringsAsFactors = F)
totAPAinRNAg=read.table("../data/mol_overlap/APA2molTotal/TotAPAqtlsPvalRNAg.txt", header = T, stringsAsFactors = F)
totAPAinRibo=read.table("../data/mol_overlap/APA2molTotal/TotAPAqtlsPvalribo.txt", header = T, stringsAsFactors = F)
totAPAinProt=read.table("../data/mol_overlap/APA2molTotal/TotAPAqtlsPvalProtein.txt", header = T, stringsAsFactors = F)
allOverlap_T=totAPAinsu30 %>% full_join(totAPAinsu60, by=c("Gene.name", "sid")) %>% full_join(totAPAinRNA, by=c("Gene.name", "sid")) %>% full_join(totAPAinRNAg, by=c("Gene.name", "sid")) %>% full_join(totAPAinRibo, by=c("Gene.name", "sid")) %>% full_join(totAPAinProt, by=c("Gene.name", "sid"))
colnames(allOverlap_T)=c("Gene.name", "sid", "su30", "su60", "RNA", "RNAg", "ribo", "prot")
plot(sort(allOverlap_T$prot))
Version | Author | Date |
---|---|---|
5649809 | Briana Mittleman | 2018-10-22 |
plot(allOverlap_T$RNA ~ allOverlap_T$prot)
Version | Author | Date |
---|---|---|
5649809 | Briana Mittleman | 2018-10-22 |
I want to make a ggplot of these where I color them by RNA pvalue:
allOverlap_T_lowP=allOverlap_T %>% dplyr::filter(prot<.05)
ggplot(allOverlap_T_lowP, aes(x=RNA, y=prot)) + geom_point()+ geom_text(aes(label=Gene.name),hjust=0, vjust=0) + geom_vline(xintercept = .05, col="red")
Version | Author | Date |
---|---|---|
5649809 | Briana Mittleman | 2018-10-22 |
ggplot(allOverlap_T_lowP, aes(x=RNAg, y=prot)) + geom_point()+ geom_text(aes(label=Gene.name),hjust=0, vjust=0) + geom_vline(xintercept = .05, col="red")
Version | Author | Date |
---|---|---|
5649809 | Briana Mittleman | 2018-10-22 |
I can use these to look for examples of SNPs that are significant in prot but not in RNA.
Look at some of these:
Total RNA:
* SACM1L
* EBI3
* FBXL18
* PSMF1
* COX17
Total RNAg:
* EBI3
* FBXL18
* APBB1IP * PSMF1
Look at some examples of genes that come up in both.
EBI3 peak152751 19:4236475
Expressed in B lymphocytes in response to EB virus.
grep EBI3 /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000105246
python createQTLsnpAPAPhenTable.py 19 19:4236475 peak152751 Total
python createQTLsnpAPAPhenTable.py 19 19:4236475 peak152751 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "19" "19:4236475" "ENSG00000105246"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*19:4236475* .
plotQTL_func(SNP="19:4236475", peak="peak152751", gene="ENSG00000105246")
FBXL18 peak291746 7:5524129
“The protein encoded by this gene is a member of a family of proteins that contain an approximately 40-amino acid F-box motif. This motif is important for interaction with SKP1 and for targeting some proteins for degradation.” genecards.org
grep FBXL18 /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000155034
python createQTLsnpAPAPhenTable.py 7 7:5524129 peak291746 Total
python createQTLsnpAPAPhenTable.py 7 7:5524129 peak291746 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "7" "7:5524129" "ENSG00000155034"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*7:5524129* .
plotQTL_func(SNP="7:5524129", peak="peak291746", gene="ENSG00000155034")
Warning: Removed 4 rows containing non-finite values (stat_boxplot).
Warning: Removed 4 rows containing non-finite values (stat_compare_means).
Warning: Removed 4 rows containing missing values (geom_point).
This gene codes the 26S proteasome.
grep PSMF1 /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000125818
python createQTLsnpAPAPhenTable.py 20 20:1131308 peak193648 Total
python createQTLsnpAPAPhenTable.py 20 20:1131308 peak193648 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "20" "20:1131308" "ENSG00000125818"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*20:1131308* .
plotQTL_func(SNP="20:1131308", peak="peak193648", gene="ENSG00000125818")
Warning: Removed 2 rows containing non-finite values (stat_boxplot).
Warning: Removed 2 rows containing non-finite values (stat_compare_means).
Warning: Removed 2 rows containing missing values (geom_point).
I want to know the number of these that are <.05 in protien and above .1 in RNA
allOverlap_T_lowP_highRNA=allOverlap_T %>% dplyr::filter(prot<.05) %>% dplyr::filter(RNA>.05)
allOverlap_T_lowP_highRNAg=allOverlap_T %>% dplyr::filter(prot<.05) %>% dplyr::filter(RNAg>.05)
8 snps with < .05 for protein. Of those 6 have RNA pvalues greater than .05
6/8
[1] 0.75
nucAPAinsu30=read.table("../data/mol_overlap/APA2molNuclear/NucAPAqtlsPval4su30.txt", header = T, stringsAsFactors = F)
nucAPAinsu60=read.table("../data/mol_overlap/APA2molNuclear/NucAPAqtlsPval4su60.txt", header = T, stringsAsFactors = F)
nucAPAinRNA=read.table("../data/mol_overlap/APA2molNuclear/NucAPAqtlsPvalRNA.txt", header = T, stringsAsFactors = F)
nucAPAinRNAg=read.table("../data/mol_overlap/APA2molNuclear/NucAPAqtlsPvalRNAg.txt", header = T, stringsAsFactors = F)
nucAPAinRibo=read.table("../data/mol_overlap/APA2molNuclear/NucAPAqtlsPvalribo.txt", header = T, stringsAsFactors = F)
nucAPAinProt=read.table("../data/mol_overlap/APA2molNuclear/NucAPAqtlsPvalProtein.txt", header = T, stringsAsFactors = F)
allOverlap_N=nucAPAinsu30 %>% full_join(nucAPAinsu60, by=c("Gene.name", "sid")) %>% full_join(nucAPAinRNA, by=c("Gene.name", "sid")) %>% full_join(nucAPAinRNAg, by=c("Gene.name", "sid")) %>% full_join(nucAPAinRibo, by=c("Gene.name", "sid")) %>% full_join(nucAPAinProt, by=c("Gene.name", "sid"))
colnames(allOverlap_N)=c("Gene.name", "sid", "su30", "su60", "RNA", "RNAg", "ribo", "prot")
#subset by prot < .05
allOverlap_N_lowP=allOverlap_N %>% dplyr::filter(prot<.05)
ggplot(allOverlap_N_lowP, aes(x=RNA, y=prot)) + geom_point()+ geom_text(aes(label=Gene.name),hjust=0, vjust=0)+ geom_vline(xintercept = .05, col="red")
Version | Author | Date |
---|---|---|
5649809 | Briana Mittleman | 2018-10-22 |
ggplot(allOverlap_N_lowP, aes(x=RNAg, y=prot)) + geom_point()+ geom_text(aes(label=Gene.name),hjust=0, vjust=0)+ geom_vline(xintercept = .05, col="red")
Version | Author | Date |
---|---|---|
5649809 | Briana Mittleman | 2018-10-22 |
allOverlap_N_lowP_highRNA=allOverlap_N %>% dplyr::filter(prot<.05) %>% dplyr::filter(RNA>.05)
allOverlap_N_lowP_highRNAg=allOverlap_N %>% dplyr::filter(prot<.05) %>% dplyr::filter(RNAg>.05)
39 snps with < .05 for protein. Of those 28 have RNA pvalues greater than .05
28/39
[1] 0.7179487
inBothN= allOverlap_N_lowP_highRNAg %>% inner_join(allOverlap_N_lowP_highRNA, by=c("Gene.name", "sid", "su30", "su60", "RNA", "RNAg", "ribo", "prot")) %>% arrange(desc(RNA))
inBothN$Gene.name[1:5]
[1] "MSMO1" "LYAR" "CD2BP2" "KDM2A" "RINT1"
contains metal binding motifs, known alternative splice isoforms
grep MSMO1 /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000052802
python createQTLsnpAPAPhenTable.py 4 4:166260601 peak249109 Total
python createQTLsnpAPAPhenTable.py 4 4:166260601 peak249109 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "4" "4:166260601" "ENSG00000052802"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*4:166260601* .
plotQTL_func(SNP="4:166260601", peak="peak249109", gene="ENSG00000052802")
Warning: Removed 3 rows containing non-finite values (stat_boxplot).
Warning: Removed 3 rows containing non-finite values (stat_compare_means).
Warning: Removed 3 rows containing missing values (geom_point).
involved in processing pre-rRNA
grep LYAR /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000145220
python createQTLsnpAPAPhenTable.py 4 4:4196045 peak235215 Total
python createQTLsnpAPAPhenTable.py 4 4:4196045 peak235215 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "4" "4:4196045" "ENSG00000145220"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*4:4196045* .
plotQTL_func(SNP="4:4196045", peak="peak235215", gene="ENSG00000145220")
CD2BP2 peak122237 16:29898001
From genecards: “in the cytoplasm, the encoded protein binds the cytoplasmic tail of human surface antigen CD2 via its C-terminal GYF domain, and regulate CD2-triggered T lymphocyte activation. In the nucleus, this protein is a component of the U5 small nuclear ribonucleoprotein complex and is involved in RNA splicing.”
grep CD2BP2 /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000169217
python createQTLsnpAPAPhenTable.py 16 16:29898001 peak122237 Total
python createQTLsnpAPAPhenTable.py 16 16:29898001 peak122237 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "16" "16:29898001" "ENSG00000169217"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*16:29898001* .
plotQTL_func(SNP="16:29898001", peak="peak122237", gene="ENSG00000169217")
Warning: Removed 5 rows containing non-finite values (stat_boxplot).
Warning: Removed 5 rows containing non-finite values (stat_compare_means).
Warning: Removed 5 rows containing missing values (geom_point).
KDM2A peak55622 11:66851583
grep KDM2A /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000173120
python createQTLsnpAPAPhenTable.py 11 11:66851583 peak55622 Total
python createQTLsnpAPAPhenTable.py 11 11:66851583 peak55622 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "11" "11:66851583" "ENSG00000173120"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*11:66851583* .
plotQTL_func(SNP="11:66851583", peak="peak55622", gene="ENSG00000173120")
Warning: Removed 8 rows containing non-finite values (stat_boxplot).
Warning: Removed 8 rows containing non-finite values (stat_compare_means).
Warning: Removed 8 rows containing missing values (geom_point).
RINT1 peak303436 7:105155320
Interacts with double strand break repair protiens, regulates cell cycle and telomere length
grep RINT1 /project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt
#ENSG00000135249
python createQTLsnpAPAPhenTable.py 7 7:105155320 peak303436 Total
python createQTLsnpAPAPhenTable.py 7 7:105155320 peak303436 Nuclear
sbatch run_createQTLsnpMolPhenTable.sh "7" "7:105155320" "ENSG00000135249"
#into apaExamp
scp brimittleman@midway2.rcc.uchicago.edu:/project2/gilad/briana/threeprimeseq/data/ApaQTL_examples/*7:105155320* .
plotQTL_func(SNP="7:105155320", peak="peak303436", gene="ENSG00000135249")
Warning: Removed 2 rows containing non-finite values (stat_boxplot).
Warning: Removed 2 rows containing non-finite values (stat_compare_means).
Warning: Removed 2 rows containing missing values (geom_point).
In the next step I need to add significance to the boxplots and think more about the significance cutoffs.
Maybe I can compare 2 other phenotypes for <.05 and >.05 to see if the percentage is less than what I see for RNA and protein.
sigProt=allOverlap_N_lowP %>% nrow()
paste("Sig Prot", sigProt, sep=" ")
[1] "Sig Prot 39"
allOverlap_N_lowP_higrna=allOverlap_N %>% dplyr::filter(prot<.05) %>% dplyr::filter(RNA>.05) %>%nrow()
paste("Sig Prot not RNA", allOverlap_N_lowP_higrna, sep=" ")
[1] "Sig Prot not RNA 28"
allOverlap_N_lowP_higribo=allOverlap_N %>% dplyr::filter(prot<.05) %>% dplyr::filter(ribo>.05) %>%nrow()
paste("Sig Prot not ribo", allOverlap_N_lowP_higribo, sep=" ")
[1] "Sig Prot not ribo 23"
allOverlap_N_lowP_higsu30=allOverlap_N %>% dplyr::filter(prot<.05) %>% dplyr::filter(su30>.05) %>% nrow()
paste("Sig Prot not 4su30", allOverlap_N_lowP_higsu30, sep=" ")
[1] "Sig Prot not 4su30 31"
allOverlap_N_lowP_higsu60=allOverlap_N %>% dplyr::filter(prot<.05) %>% dplyr::filter(su60>.05) %>% nrow()
paste("Sig Prot not 4su60", allOverlap_N_lowP_higsu60, sep=" ")
[1] "Sig Prot not 4su60 27"
sigProtT=allOverlap_T_lowP %>% nrow()
paste("Sig Prot", sigProtT, sep=" ")
[1] "Sig Prot 8"
allOverlap_T_lowP_higrna=allOverlap_T %>% dplyr::filter(prot<.05) %>% dplyr::filter(RNA>.05) %>%nrow()
paste("Sig Prot not RNA", allOverlap_T_lowP_higrna, sep=" ")
[1] "Sig Prot not RNA 6"
allOverlap_T_lowP_higribo=allOverlap_T %>% dplyr::filter(prot<.05) %>% dplyr::filter(ribo>.05) %>%nrow()
paste("Sig Prot not ribo", allOverlap_T_lowP_higribo, sep=" ")
[1] "Sig Prot not ribo 5"
allOverlap_T_lowP_higsu30=allOverlap_T %>% dplyr::filter(prot<.05) %>% dplyr::filter(su30>.05) %>% nrow()
paste("Sig Prot not 4su30", allOverlap_T_lowP_higsu30, sep=" ")
[1] "Sig Prot not 4su30 6"
allOverlap_T_lowP_higsu60=allOverlap_T %>% dplyr::filter(prot<.05) %>% dplyr::filter(su60>.05) %>% nrow()
paste("Sig Prot not 4su60", allOverlap_T_lowP_higsu60, sep=" ")
[1] "Sig Prot not 4su60 5"
In order to think about this more broadly I am going to plot overlaps:
Given all of these are APA qtls, how many are significant in:
Do this first for total:
p_N=allOverlap_N %>% filter(prot<.05) %>% nrow()
RP_N=allOverlap_N %>% filter(prot<.05 & RNA <.05) %>% nrow()
RnotP_N=allOverlap_N %>% filter(prot>.05 & RNA <.05) %>% nrow()
notRnotP_N=allOverlap_N %>% filter(prot>.05 & RNA >.05) %>% nrow()
notRP_N= allOverlap_N %>% filter(prot<.05 & RNA >.05) %>% nrow()
overlapNames=c("Protein", "RNAandProtein", "RNAnotProt", "Neither", "ProteinnotRNA")
NucRPoverlap=c(p_N/nrow(allOverlap_N),RP_N/nrow(allOverlap_N), RnotP_N/nrow(allOverlap_N), notRnotP_N/nrow(allOverlap_N),notRP_N/nrow(allOverlap_N) )
NucOverlapDF=data.frame(overlapNames,NucRPoverlap)
ggplot(NucOverlapDF, aes(x=overlapNames, y=NucRPoverlap)) + geom_bar(stat="identity")
Version | Author | Date |
---|---|---|
d59b3c1 | Briana Mittleman | 2018-10-24 |
DO the same for total:
p_T=allOverlap_T %>% filter(prot<.05) %>% nrow()
RP_T=allOverlap_T %>% filter(prot<.05 & RNA <.05) %>% nrow()
RnotP_T=allOverlap_T %>% filter(prot>.05 & RNA <.05) %>% nrow()
notRnotP_T=allOverlap_T %>% filter(prot>.05 & RNA >.05) %>% nrow()
notRP_T= allOverlap_T %>% filter(prot<.05 & RNA >.05) %>% nrow()
TotRPoverlap=c(p_T/nrow(allOverlap_T),RP_T/nrow(allOverlap_T), RnotP_T/nrow(allOverlap_T), notRnotP_T/nrow(allOverlap_T),notRP_T/nrow(allOverlap_T))
TotOverlapDF=data.frame(overlapNames,TotRPoverlap)
ggplot(TotOverlapDF, aes(x=overlapNames, y=TotRPoverlap)) + geom_bar(stat="identity")
Version | Author | Date |
---|---|---|
d59b3c1 | Briana Mittleman | 2018-10-24 |
allOverlapDF=TotOverlapDF %>% full_join(NucOverlapDF, by="overlapNames")
allOverlapDF_melt=melt(allOverlapDF, id.vars="overlapNames")
ggplot(allOverlapDF_melt, aes(x=overlapNames, y=value, by=variable, fill=variable)) + geom_bar(stat="identity", position="dodge") + scale_fill_manual(values=c("darkviolet", "deepskyblue3")) + labs(y="Proportion of APA QTLs", x="Category")
Version | Author | Date |
---|---|---|
d59b3c1 | Briana Mittleman | 2018-10-24 |
oT=overlapplotT=draw.pairwise.venn(area1=.08, area2=.07, cross.area = .02, category = c("Protein", "RNA"),lty = rep("solid", 2), fill = c("Blue", "Orange"), alpha = rep(0.5, 2), cat.pos = c(0, 0), cat.dist = rep(0.025, 2), euler.d = T, scaled=T)
Version | Author | Date |
---|---|---|
d59b3c1 | Briana Mittleman | 2018-10-24 |
png("../output/plots/overlapProtRNAvenT.png")
grid.arrange(gTree(children=oT), top="Total: Protein and RNA QTL overlap", bottom="Neither=.37")
dev.off()
quartz_off_screen
2
oN=overlapplotN=draw.pairwise.venn(area1=.056, area2=.096, cross.area = .016, category = c("Protein", "RNA"),lty = rep("solid", 2), fill = c("Blue", "Orange"), alpha = rep(0.5, 2), cat.pos = c(0, 0), cat.dist = rep(0.025, 2), euler.d = T, scaled=T)
Version | Author | Date |
---|---|---|
d59b3c1 | Briana Mittleman | 2018-10-24 |
png("../output/plots/overlapProtRNAvenN.png")
grid.arrange(gTree(children=oN), top="Nuclear:Protein and RNA QTL overlap", bottom="Neither=.38")
dev.off()
quartz_off_screen
2
This doesnt look statistically significant but it does look like the total fraction has more pQTLs that are not eQTLs and in the nuclear you get the opposite effect.
sessionInfo()
R version 3.5.1 (2018-07-02)
Platform: x86_64-apple-darwin15.6.0 (64-bit)
Running under: macOS 10.14.1
Matrix products: default
BLAS: /Library/Frameworks/R.framework/Versions/3.5/Resources/lib/libRblas.0.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/3.5/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] grid stats graphics grDevices utils datasets methods
[8] base
other attached packages:
[1] bindrcpp_0.2.2 gridExtra_2.3 VennDiagram_1.6.20
[4] futile.logger_1.4.3 ggpubr_0.1.8 magrittr_1.5
[7] cowplot_0.9.3 data.table_1.11.8 forcats_0.3.0
[10] stringr_1.4.0 dplyr_0.7.6 purrr_0.2.5
[13] readr_1.1.1 tidyr_0.8.1 tibble_1.4.2
[16] ggplot2_3.0.0 tidyverse_1.2.1 workflowr_1.2.0
loaded via a namespace (and not attached):
[1] tidyselect_0.2.4 reshape2_1.4.3 haven_1.1.2
[4] lattice_0.20-35 colorspace_1.3-2 htmltools_0.3.6
[7] yaml_2.2.0 rlang_0.2.2 pillar_1.3.0
[10] glue_1.3.0 withr_2.1.2 RColorBrewer_1.1-2
[13] lambda.r_1.2.3 modelr_0.1.2 readxl_1.1.0
[16] bindr_0.1.1 plyr_1.8.4 munsell_0.5.0
[19] gtable_0.2.0 cellranger_1.1.0 rvest_0.3.2
[22] evaluate_0.13 labeling_0.3 knitr_1.20
[25] broom_0.5.0 Rcpp_0.12.19 formatR_1.5
[28] scales_1.0.0 backports_1.1.2 jsonlite_1.6
[31] fs_1.2.6 hms_0.4.2 digest_0.6.17
[34] stringi_1.2.4 rprojroot_1.3-2 cli_1.0.1
[37] tools_3.5.1 lazyeval_0.2.1 futile.options_1.0.1
[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_1.11 httr_1.3.1 rstudioapi_0.9.0
[49] R6_2.3.0 nlme_3.1-137 git2r_0.24.0
[52] compiler_3.5.1