Last updated: 2019-04-10

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Knit directory: threeprimeseq/analysis/

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    Modified:   analysis/unexplainedeQTL_analysis.Rmd
    Modified:   code/Snakefile

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File Version Author Date Message
Rmd 70732bb Briana Mittleman 2019-04-10 add scripts for new snake

I need to make general scripts for the new processed snakefile:

filterBamBasedonWasp_general.py

def main(Bamin, out):
    okRead={}
    #pysam to read in bam allignments
    bamfile = pysam.AlignmentFile(Bamin, "rb")
    finalBam =  pysam.AlignmentFile(out, "wb", template=bamfile)
    n=0
    k=0
    #read name is the first col in each bam file
    for read in bamfile.fetch():
        #last piece is always the right piece  
        #vw=read.split(\t)[-1]
        if read.has_tag('vW'):
            x= read.get_tag('vW')
            print(x)
            if x == 1:
                k+=1
                finalBam.write(read)
            else:
                n+=1
                continue
        else:
          finalBam.write(read)
  
    print("with wv" + n)
    print("pass filter" + k)
    bamfile.close()
    finalBam.close()
    
    
    
if __name__ == "__main__":
    import sys, pysam
    inBam=sys.argv[1]
    outBam=sys.argv[2]
    main(inBam, outBam)
    

Upstream10Bases_general.py

#python  
def main(Fin, Fout):
  outBed=open(Fout, "w")
  chrom_lengths=open("/project2/gilad/briana/genome_anotation_data/chrom_lengths2.sort.bed","r")
  #make a dictionary with chrom lengths
  length_dic={}
  for i in chrom_lengths:
    chrom, start, end = i.split()
    length_dic[str(chrom)]=int(end)  

#write file 
  for ln in open(Fin):
    chrom, start, end, name, score, strand = ln.split()
    chrom=str(chrom)
    if strand=="+":
      start_new=int(start)-10
      if start_new <= 1:
        start_new = 0 
      end_new= int(start)
      if end_new == 0:
        end_new=1
      outBed.write("%s\t%d\t%d\t%s\t%s\t%s\n"%(chrom, start_new, end_new, name, score, strand))
    if strand == "-":
      start_new=int(end)
      end_new=int(end) + 10
      if end_new >= length_dic[chrom]:
        end_new = length_dic[chrom] 
        start_new=end_new-1 
      outBed.write("%s\t%d\t%d\t%s\t%s\t%s\n"%(chrom, start_new, end_new, name, score, strand))
  outBed.close()  

if __name__ == "__main__":
    import sys
    inFile = sys.argv[1]
    outFile = sys.argv[2]
    main(inFile, outFile)

filterMissprimingInNuc10_gen.py

def main(Fin, Fout):
  outBed=open(Fout, "w")
  inBed=open(Fin, "r")
  for ind, ln in enumerate(inBed):
    if ind >=1:
      chrom,start, end, name, score, strand, pctAT, pctGC, A, C, G, T, N, Other, Length, Sequence = ln.split()
      Tperc= float(T) / float(Length)
      if Tperc < .7:
          if "TTTTTT" not in Sequence:
              start_new=int(start)
              end_new=int(end)
              outBed.write("%s\t%d\t%d\t%s\t%s\t%s\n"%(chrom, start_new, end_new , name, score, strand))
  outBed.close()

if __name__ == "__main__":
    import sys
    inFile = sys.argv[1]
    outFile=sys.argv[2]
    main(inFile, outFile)

filterSortBedbyCleanedBed_gen.R

#!/bin/rscripts

# usage: Rscirpt --vanilla  filterSortBedbyCleanedBed_gen.R bedfile cleannuc outfile

#this script takes in the sorted bed file and the clean reads, it will clean the bed file   


library(dplyr)
library(tidyr)
library(data.table)


args = commandArgs(trailingOnly=TRUE)
bed=args[1]
clean= args[2]
output=args[3]


bedFile=fread(bed, col.names = c("Chrom", "start", "end", "name", "score", "strand"))

cleanFile=fread(clean, col.names = c("Chrom", "start", "end", "name", "score", "strand"))

intersection=bedFile %>% semi_join(cleanFile, by="name")

fwrite(intersection, file=output,quote = F, col.names = F, row.names = F, sep="\t")

filterBamforMP.pysam2_gen.py

#!/usr/bin/env python


def main(Bin, Bamin, out):
    okRead={}
    for ln in open(Bin, "r"):
        chrom, start_new , end_new , name, score, strand = ln.split()
        okRead[name] = ""
    #pysam to read in bam allignments
    bamfile = pysam.AlignmentFile(Bamin, "rb")
    finalBam =  pysam.AlignmentFile(out, "wb", template=bamfile)
    #read name is the first col in each bam file
    n=0
    for read in bamfile.fetch():
        read_name=read.query_name
        #if statement about name  
        if read_name in okRead.keys():
            finalBam.write(read)
        if n % 1000==0 : print(n)
        n+=1 
    bamfile.close()
    finalBam.close()

    
if __name__ == "__main__":
    import sys, pysam
    inBed= sys.argv[1]
    inBam=sys.argv[2]
    outBam=sys.argv[3]
    main(inBed, inBam, outBam)


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_1.0.0      digest_0.6.18   rprojroot_1.3-2
 [5] backports_1.1.3 git2r_0.24.0    magrittr_1.5    evaluate_0.13  
 [9] stringi_1.3.1   fs_1.2.6        whisker_0.3-2   rmarkdown_1.11 
[13] tools_3.5.1     stringr_1.4.0   glue_1.3.0      xfun_0.5       
[17] yaml_2.2.0      compiler_3.5.1  htmltools_0.3.6 knitr_1.21