Mercurial > repos > arkarachai-fungtammasan > microsatellite_ngs
view PEsortedSAM2readprofile.py @ 7:3c05abb4452e default tip
add missing files
author | devteam@galaxyproject.org |
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date | Wed, 22 Apr 2015 12:22:50 -0400 |
parents | 20ab85af9505 |
children |
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#!/usr/bin/env python import sys from galaxy import eggs import pkg_resources pkg_resources.require( "bx-python" ) import bx.seq.twobit ##output columns: read_name chr prefix_start prefix_end TR_start TR_end suffix_start suffix_end TR_length TR_sequence samf = open(sys.argv[1],'r') #assumes sam file is sorted by readname seq_path = sys.argv[2] #Path to the reference genome in 2bit format ##maxTRlength=int(sys.argv[4]) ##maxoriginalreadlength=int(sys.argv[5]) maxTRlength=int(sys.argv[3]) maxoriginalreadlength=int(sys.argv[4]) outfile=sys.argv[5] fout = open(outfile,'w') twobitfile = bx.seq.twobit.TwoBitFile( file( seq_path ) ) skipped=0 while True: read = samf.readline().strip() if not(read): #EOF reached break if read[0] == "@": #print read continue mate = samf.readline().strip() if not(mate): #EOF reached break read_elems = read.split() mate_elems = mate.split() read_name = read_elems[0].strip() mate_name = mate_elems[0].strip() while True: if read_name == mate_name: break elif read_name != mate_name: #print >>sys.stderr, "Input SAM file doesn't seem to be sorted by readname. Please sort and retry." #break skipped += 1 read = mate read_elems = mate_elems mate = samf.readline().strip() read_name = read_elems[0].strip() mate_name = mate_elems[0].strip() if not(mate): #EOF reached break mate_elems = mate.split() #extract XT:A tag #for e in read_elems: # if e.startswith('XT:A'): # read_xt = e #for e in mate_elems: # if e.startswith('XT:A'): # mate_xt = e #if 'XT:A:U' not in read_elems or 'XT:A:U' not in mate_elems: #both read and it's mate need to be mapped uniquely # continue read_chr = read_elems[2] read_start = int(read_elems[3]) read_cigar = read_elems[5] if len(read_cigar.split('M')) != 2: #we want perfect matches only..cigar= <someInt>M continue read_len = int(read_cigar.split('M')[0]) mate_chr = mate_elems[2] mate_start = int(mate_elems[3]) mate_cigar = mate_elems[5] if len(mate_cigar.split('M')) != 2: #we want perfect matches only..cigar= <someInt>M continue mate_len = int(mate_cigar.split('M')[0]) if read_chr != mate_chr: # check that they were mapped to the same chromosome continue if abs(read_start - mate_start) > (maxoriginalreadlength+maxTRlength): continue if read_start < mate_start: pre_s = read_start-1 pre_e = read_start-1+read_len tr_s = read_start-1+read_len tr_e = mate_start-1 suf_s = mate_start-1 suf_e = mate_start-1+mate_len else: pre_s = mate_start-1 pre_e = mate_start-1+mate_len tr_s = mate_start-1+mate_len tr_e = read_start-1 suf_s = read_start-1 suf_e = read_start-1+read_len tr_len = abs(tr_e - tr_s) if tr_len > maxTRlength: continue if pre_e >= suf_s: #overlapping prefix and suffix continue tr_ref_seq = twobitfile[read_chr][tr_s:tr_e] ##print >>fout, "%s\t%s\t%s\t%s\t%s\t%s\t%s\t%s\t%s\t%s" %(read_name,read_chr,pre_s,pre_e,tr_s,tr_e,suf_s,suf_e,tr_len,tr_ref_seq) fout.writelines('\t'.join(map(str,[read_name,read_chr,pre_s,pre_e,tr_s,tr_e,suf_s,suf_e,tr_len,tr_ref_seq]))+'\n') print "Skipped %d unpaired reads" %(skipped)