Exemple #1
0
 def hmmbuild(alignment, outfile, name=None, **kwargs):
     unlink_file = False
     if isinstance(alignment, str): msafile = alignment
     elif isinstance(alignment, MultipleSeqAlignment):
         msafile = AlignmentUtils.mktmp(alignment)
         if not msafile: return False
         unlink_file = True
     else:
         print 'Alignment must be either a filename or an instance of MultipleSeqAlignment'
         return False
     if not name: name = FilenameParser.strip_ext(os.path.basename(outfile))
     ret = run_cline(HMMBuildCommandline(input=msafile,
                                         out=outfile,
                                         n=name,
                                         cpu=cpu_count,
                                         seed=0,
                                         **kwargs),
                     _msg='Unable to build HMM profile')
     if unlink_file: os.unlink(msafile)
     return ret
Exemple #2
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 def hmmbuild(alignment, outfile, name=None, **kwargs):
     msafile = AlignmentUtils.mktmp(alignment)
     if not name: name = FilenameParser.strip_ext(outfile)
     return run_cline(HMMBuildCommandline(input=msafile, out=outfile, 
                                          n=name, cpu=cpu_count, seed=0, **kwargs), 
                      _msg = 'Unable to build HMM profile')
Exemple #3
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 def _main(self):
     min_prod = 400
     silva_db = '/home/allis/Documents/INMI/SILVA-DB/SILVA_123_SSURef_Nr99_tax_silva.fasta'
     alifile = '/home/allis/Documents/INMI/SunS-metagenome/Bathy/BA2_SunS_16S.aln.fasta'
     add_filename = FilenameParser.strip_ext(alifile)+'.with_additions.fasta'
     outgroups = ['Thermococcus_chitonophagus', 'SMTZ1-55', 'contig72135_1581_sunspring_meta']
     add = ['KF836721.1.1270','EU635905.1.1323']
     exclude = []#['Thermococcus_chitonophagus', 'SMTZ1-55', 'BA1-16S', 'contig72135_1581_sunspring_meta']
     #load alignment
     if os.path.isfile(add_filename): 
         alifile = add_filename
         add_filename = ''
     with user_message('Loadding initial alignment...', '\n'):
         orig_ali = AlignmentUtils.load_first(alifile)
         if not orig_ali: return 1
     #load homologs
     if add_filename:
         with user_message('Loadding additional sequences...', '\n'):
             add_seqs = []
             db = SeqView()
             if db.load(silva_db):
                 for sid in add:
                     seq = db.get(sid)
                     if seq: add_seqs.append(seq)
                     else: print '%s not found in %s' % (sid, silva_db)
         #realign data if needed
         if add_seqs:
             with user_message('Realigning data...', '\n'):
                 add_filename = FilenameParser.strip_ext(alifile)+'.with_additions.fasta'
                 AlignmentUtils.align(list(orig_ali)+add_seqs, add_filename)
                 orig_ali = AlignmentUtils.load_first(add_filename)
                 if not orig_ali: return 2
     #process the alignment
     ali = orig_ali.remove(*exclude).trim()
     for out in outgroups:
         if not ali.index(out):
             print '%s not found in the alignment' % out
             return 3
     ali.sort(key=lambda r: 'zzzzzzzz' if r.id in outgroups else r.id)
     ali_len = ali.get_alignment_length()
     AlignmentUtils.save(ali, '/home/allis/Documents/INMI/SunS-metagenome/Bathy/BA2_SunS_16S.aln.trimmed.fasta')
     args = dict(plen = (20,40),
                 max_mismatches = 8,
                 min_match_mismatches = 1,
                 first_match_mismatches = 1,
                 first_may_match = 1,
                 AT_first=True,
                 outgroup=len(outgroups))
     fprimers = self._find_primers(ali, **args)
     rprimers = self._find_primers(ali.reverse_complement(), **args)
     pairs = []
     for i, (fs, fp) in enumerate(fprimers):
         start = fs
         fprimer = Primer.from_sequences(fp[:-1], 1, 'SSBaF%d' % fs)
         for _j, (rs, rp) in enumerate(rprimers):
             end = ali_len-rs
             if end-start <= min_prod: continue
             pairs.append((fprimer, Primer.from_sequences(rp[:-1], 1, 'SSBaR%d' % (ali_len-rs+1))))
     if not pairs:
         print '\nNo suitable primer pairs found'
         return 3
     added = set()
     for i, (fp, rp) in enumerate(pairs):
         print '\npair %d' % (i+1)
         print '%s: %s' % (fp.id, fp)
         print '%s: %s' % (rp.id, rp)
         if fp.id not in added:
             orig_ali.append(fp.master_sequence+'-'*(orig_ali.get_alignment_length()-len(fp)))
             added.add(fp.id)
         if rp.id not in added:
             orig_ali.append(copy_attrs(rp.master_sequence,
                                        rp.master_sequence.reverse_complement())+
                             '-'*(orig_ali.get_alignment_length()-len(rp)))
             added.add(rp.id)
     print
     orig_ali = AlignmentUtils.align(orig_ali)
     AlignmentUtils.save(orig_ali, '/home/allis/Documents/INMI/SunS-metagenome/Bathy/BA2_SunS_16S.with_primers.aln.fasta')
     print 'Done'
Exemple #4
0
 def _main(self):
     min_prod = 400
     silva_db = '/home/allis/Documents/INMI/SILVA-DB/SILVA_123_SSURef_Nr99_tax_silva.fasta'
     alifile = '/home/allis/Documents/INMI/SunS-metagenome/Bathy/BA2_SunS_16S.aln.fasta'
     add_filename = FilenameParser.strip_ext(
         alifile) + '.with_additions.fasta'
     outgroups = [
         'Thermococcus_chitonophagus', 'SMTZ1-55',
         'contig72135_1581_sunspring_meta'
     ]
     add = ['KF836721.1.1270', 'EU635905.1.1323']
     exclude = [
     ]  #['Thermococcus_chitonophagus', 'SMTZ1-55', 'BA1-16S', 'contig72135_1581_sunspring_meta']
     #load alignment
     if os.path.isfile(add_filename):
         alifile = add_filename
         add_filename = ''
     with user_message('Loadding initial alignment...', '\n'):
         orig_ali = AlignmentUtils.load_first(alifile)
         if not orig_ali: return 1
     #load homologs
     if add_filename:
         with user_message('Loadding additional sequences...', '\n'):
             add_seqs = []
             db = SeqView()
             if db.load(silva_db):
                 for sid in add:
                     seq = db.get(sid)
                     if seq: add_seqs.append(seq)
                     else: print '%s not found in %s' % (sid, silva_db)
         #realign data if needed
         if add_seqs:
             with user_message('Realigning data...', '\n'):
                 add_filename = FilenameParser.strip_ext(
                     alifile) + '.with_additions.fasta'
                 AlignmentUtils.align(
                     list(orig_ali) + add_seqs, add_filename)
                 orig_ali = AlignmentUtils.load_first(add_filename)
                 if not orig_ali: return 2
     #process the alignment
     ali = orig_ali.remove(*exclude).trim()
     for out in outgroups:
         if not ali.index(out):
             print '%s not found in the alignment' % out
             return 3
     ali.sort(key=lambda r: 'zzzzzzzz' if r.id in outgroups else r.id)
     AlignmentUtils.save(
         ali,
         '/home/allis/Documents/INMI/SunS-metagenome/Bathy/BA2_SunS_16S.aln.trimmed.fasta'
     )
     args = dict(plen=(20, 40),
                 max_mismatches=8,
                 min_match_mismatches=1,
                 first_match_mismatches=1,
                 first_may_match=1,
                 AT_first=True,
                 outgroup=len(outgroups))
     fprimers = PrimerFinder.find_discriminating_primers(ali, **args)
     rprimers = PrimerFinder.find_discriminating_primers(ali,
                                                         reverse=True,
                                                         **args)
     pairs = PrimerFinder.compile_pairs(fprimers, rprimers, min_prod,
                                        'SSBa')
     if not pairs:
         print '\nNo suitable primer pairs found'
         return 3
     PrimerFinder.print_pairs(pairs)
     orig_ali = PrimerFinder.add_pairs_to_alignment(pairs, orig_ali)
     AlignmentUtils.save(
         orig_ali,
         '/home/allis/Documents/INMI/SunS-metagenome/Bathy/BA2_SunS_16S.with_primers.aln.fasta'
     )
     print 'Done'