annotate PEsortedSAM2readprofile.py @ 7:3c05abb4452e default tip

add missing files
author devteam@galaxyproject.org
date Wed, 22 Apr 2015 12:22:50 -0400
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1 #!/usr/bin/env python
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2
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3 import sys
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4 from galaxy import eggs
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5 import pkg_resources
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6 pkg_resources.require( "bx-python" )
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7 import bx.seq.twobit
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8
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9 ##output columns: read_name chr prefix_start prefix_end TR_start TR_end suffix_start suffix_end TR_length TR_sequence
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10
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11 samf = open(sys.argv[1],'r') #assumes sam file is sorted by readname
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12 seq_path = sys.argv[2] #Path to the reference genome in 2bit format
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13
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14 ##maxTRlength=int(sys.argv[4])
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15 ##maxoriginalreadlength=int(sys.argv[5])
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16 maxTRlength=int(sys.argv[3])
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17 maxoriginalreadlength=int(sys.argv[4])
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18 outfile=sys.argv[5]
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19 fout = open(outfile,'w')
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20
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21 twobitfile = bx.seq.twobit.TwoBitFile( file( seq_path ) )
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22
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23 skipped=0
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24 while True:
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25 read = samf.readline().strip()
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26 if not(read): #EOF reached
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27 break
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28 if read[0] == "@":
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29 #print read
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30 continue
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31 mate = samf.readline().strip()
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32 if not(mate): #EOF reached
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33 break
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34 read_elems = read.split()
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35 mate_elems = mate.split()
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36 read_name = read_elems[0].strip()
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37 mate_name = mate_elems[0].strip()
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38 while True:
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39 if read_name == mate_name:
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40 break
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41 elif read_name != mate_name:
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42 #print >>sys.stderr, "Input SAM file doesn't seem to be sorted by readname. Please sort and retry."
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43 #break
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44 skipped += 1
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45 read = mate
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46 read_elems = mate_elems
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47 mate = samf.readline().strip()
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48 read_name = read_elems[0].strip()
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49 mate_name = mate_elems[0].strip()
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50 if not(mate): #EOF reached
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51 break
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52 mate_elems = mate.split()
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53 #extract XT:A tag
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54 #for e in read_elems:
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55 # if e.startswith('XT:A'):
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56 # read_xt = e
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57 #for e in mate_elems:
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58 # if e.startswith('XT:A'):
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59 # mate_xt = e
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60 #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
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61 # continue
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62 read_chr = read_elems[2]
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63 read_start = int(read_elems[3])
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64 read_cigar = read_elems[5]
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65 if len(read_cigar.split('M')) != 2: #we want perfect matches only..cigar= <someInt>M
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66 continue
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67 read_len = int(read_cigar.split('M')[0])
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68 mate_chr = mate_elems[2]
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69 mate_start = int(mate_elems[3])
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70 mate_cigar = mate_elems[5]
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71 if len(mate_cigar.split('M')) != 2: #we want perfect matches only..cigar= <someInt>M
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72 continue
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73 mate_len = int(mate_cigar.split('M')[0])
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74 if read_chr != mate_chr: # check that they were mapped to the same chromosome
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75 continue
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76 if abs(read_start - mate_start) > (maxoriginalreadlength+maxTRlength):
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77 continue
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78 if read_start < mate_start:
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79 pre_s = read_start-1
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80 pre_e = read_start-1+read_len
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81 tr_s = read_start-1+read_len
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82 tr_e = mate_start-1
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83 suf_s = mate_start-1
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84 suf_e = mate_start-1+mate_len
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85 else:
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86 pre_s = mate_start-1
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87 pre_e = mate_start-1+mate_len
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88 tr_s = mate_start-1+mate_len
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89 tr_e = read_start-1
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90 suf_s = read_start-1
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91 suf_e = read_start-1+read_len
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92 tr_len = abs(tr_e - tr_s)
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93 if tr_len > maxTRlength:
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94 continue
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95 if pre_e >= suf_s: #overlapping prefix and suffix
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96 continue
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97 tr_ref_seq = twobitfile[read_chr][tr_s:tr_e]
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98 ##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)
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99 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')
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100
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101 print "Skipped %d unpaired reads" %(skipped)