Last updated: 2019-02-19
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Knit directory: threeprimeseq/analysis/
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File | Version | Author | Date | Message |
---|---|---|---|---|
Rmd | 2a9d059 | Briana Mittleman | 2019-02-19 | code for nom pvals |
For a lot of this project I have been looking at the relationship between APA, RNA, and protein. I want to use trhis analysis to get the nominal pvalues for the associations of the snp:gene pairs found in the APA qtl analysis. This will help me find examples and look at the distributions overall.
I want a file that has the nominal pvalues for each of the apaQTls in the total 3’, nuclear 3’, RNA, and protein. I will have to convert the gene names.
Start with a dictionary of the QTLs. It will have the snp as the key and converted gene as the value. I can then write out the associations.
I can do this seperate for RNA and protein with total and nuclear by having a script that can take all of the combinations. After I get the results I can merge them and add NAs for missing measurements.
I can ask questions like, given a snp is a apaQTL what is nom association in other pheno.
Molpval4ApaQTL.py
def main(QTL, phen, outF, phenotype):
fout=open(outF,"w")
geneNames=open("/project2/gilad/briana/genome_anotation_data/ensemble_to_genename.txt","r")
#gene name dictionary
geneDic={}
geneDicOpp={}
for i, ln in enumerate(geneNames):
if i >0:
ID=ln.split()[0]
gene=ln.split()[1]
if gene not in geneDic.keys():
geneDic[gene]=[ID]
else:
geneDic[gene].append(ID)
geneDicOpp[ID]=gene
print(geneDicOpp.keys())
#qtl dic
qtlDic={}
for ln in open(QTL,"r"):
snp=ln.split()[5]
gene=ln.split()[0].split(":")[-1].split("_")[0]
#gene_id=geneDic[gene]
qtlDic[snp]=gene
#loop over pheno
for ln in open(phen,"r"):
snp=ln.split()[1]
if snp in qtlDic.keys():
if phenotype == "RNA":
gene=ln.split()[0].split(".")[0]
if gene not in geneDicOpp.keys():
next
geneName=geneDicOpp[gene]
else:
gene=ln.split()[0]
if gene not in geneDicOpp.keys():
next
geneName=geneDicOpp[gene]
if qtlDic[snp]==geneName:
pval=ln.split()[3]
fout.write("%s\t%s\t%s\t%s\n"%(snp, gene, geneName, pval))
fout.close()
if __name__ == "__main__":
import sys
fraction = sys.argv[1]
pheno = sys.argv[2]
inQTL="/project2/gilad/briana/threeprimeseq/data/ApaQTLs/%sapaQTLs.GeneLocAnno.noMP.5perc.10FDR.txt"%(fraction)
if pheno == "RNA":
inPhen="/project2/gilad/briana/threeprimeseq/data/molecular_QTLs/nom/fastqtl_qqnorm_RNAseq_phase2.fixed.nominal.out"
if pheno =="Protein":
inPhen= "/project2/gilad/briana/threeprimeseq/data/molecular_QTLs/nom/fastqtl_qqnorm_prot_fixed.nominal.out"
out="/project2/gilad/briana/threeprimeseq/data/ApaQTLs_otherPhen/%sQTLsin%s.txt"%(fraction, pheno)
main(inQTL, inPhen, out, pheno)
Run this on all combinations:
run_Molpval4ApaQTL.sh
#!/bin/bash
#SBATCH --job-name=run_Molpval4ApaQTL
#SBATCH --account=pi-yangili1
#SBATCH --time=36:00:00
#SBATCH --output=run_Molpval4ApaQTL.out
#SBATCH --error=run_Molpval4ApaQTL.err
#SBATCH --partition=broadwl
#SBATCH --mem=30G
#SBATCH --mail-type=END
module load Anaconda3
source activate three-prime-env
python Molpval4ApaQTL.py Total RNA
python Molpval4ApaQTL.py Nuclear RNA
python Molpval4ApaQTL.py Total Protein
python Molpval4ApaQTL.py Nuclear Protein
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] stats graphics grDevices utils datasets methods base
loaded via a namespace (and not attached):
[1] workflowr_1.2.0 Rcpp_0.12.19 digest_0.6.17 rprojroot_1.3-2
[5] backports_1.1.2 git2r_0.24.0 magrittr_1.5 evaluate_0.13
[9] stringi_1.2.4 fs_1.2.6 whisker_0.3-2 rmarkdown_1.11
[13] tools_3.5.1 stringr_1.4.0 glue_1.3.0 yaml_2.2.0
[17] compiler_3.5.1 htmltools_0.3.6 knitr_1.20