def parse_hsps(self, hit_placeholders):
"""Parse a HMMER2 hsp block, beginning with the hsp table."""
# HSPs may occur in different order than the hits
# so store Hit objects separately first
unordered_hits = {}
while self.read_next():
if self.line.startswith('Alignments') or \
self.line.startswith('Histogram') or \
self.line == '//':
break
if self.line.startswith('Model') or \
self.line.startswith('Sequence') or \
self.line.startswith('--------'):
continue
id_, domain, seq_f, seq_t, seq_compl, hmm_f, hmm_t, hmm_compl, \
score, evalue = self.line.split()
frag = HSPFragment(id_, self.qresult.id)
frag.alphabet = generic_protein
if self._meta['program'] == 'hmmpfam':
frag.hit_start = int(hmm_f) - 1
frag.hit_end = int(hmm_t)
frag.query_start = int(seq_f) - 1
frag.query_end = int(seq_t)
elif self._meta['program'] == 'hmmsearch':
frag.query_start = int(hmm_f) - 1
frag.query_end = int(hmm_t)
frag.hit_start = int(seq_f) - 1
frag.hit_end = int(seq_t)
hsp = HSP([frag])
hsp.evalue = float(evalue)
hsp.bitscore = float(score)
hsp.domain_index = int(domain.split('/')[0])
if self._meta['program'] == 'hmmpfam':
hsp.hit_endtype = hmm_compl
hsp.query_endtype = seq_compl
elif self._meta['program'] == 'hmmsearch':
hsp.query_endtype = hmm_compl
hsp.hit_endtype = seq_compl
if id_ not in unordered_hits:
placeholder = [p for p in hit_placeholders if p.id_ == id_][0]
hit = placeholder.createHit([hsp])
unordered_hits[id_] = hit
else:
hit = unordered_hits[id_]
hsp.hit_description = hit.description
hit.append(hsp)
# The placeholder list is in the correct order, so use that order for
# the Hit objects in the qresult
for p in hit_placeholders:
self.qresult.append(unordered_hits[p.id_])
def _create_hits(self, hit_attrs, qid, qdesc):
"""Parses a HMMER3 hsp block, beginning with the hsp table."""
# read through until the beginning of the hsp block
self._read_until(lambda line: line.startswith('Internal pipeline') or
line.startswith('>>'))
# start parsing the hsp block
hit_list = []
while True:
if self.line.startswith('Internal pipeline'):
# by this time we should've emptied the hit attr list
assert len(hit_attrs) == 0
return hit_list
assert self.line.startswith('>>')
hid, hdesc = self.line[len('>> '):].split(' ', 1)
hdesc = hdesc.strip()
# read through the hsp table header and move one more line
self._read_until(lambda line:
line.startswith(' --- ------ ----- --------') or
line.startswith(' [No individual domains'))
self.line = read_forward(self.handle)
# parse the hsp table for the current hit
hsp_list = []
while True:
# break out of hsp parsing if there are no hits, it's the last hsp
# or it's the start of a new hit
if self.line.startswith(' [No targets detected that satisfy') or \
self.line.startswith(' [No individual domains') or \
self.line.startswith('Internal pipeline statistics summary:') or \
self.line.startswith(' Alignments for each domain:') or \
self.line.startswith('>>'):
hit_attr = hit_attrs.pop(0)
hit = Hit(hsp_list)
for attr, value in hit_attr.items():
if attr == "description":
cur_val = getattr(hit, attr)
if cur_val and value and cur_val.startswith(value):
continue
setattr(hit, attr, value)
if not hit:
hit.query_description = qdesc
hit_list.append(hit)
break
parsed = [x for x in self.line.strip().split(' ') if x]
assert len(parsed) == 16
# parsed column order:
# index, is_included, bitscore, bias, evalue_cond, evalue
# hmmfrom, hmmto, query_ends, hit_ends, alifrom, alito,
# envfrom, envto, acc_avg
frag = HSPFragment(hid, qid)
# set query and hit descriptions if they are defined / nonempty string
if qdesc:
frag.query_description = qdesc
if hdesc:
frag.hit_description = hdesc
# HMMER3 alphabets are always protein alphabets
frag.alphabet = generic_protein
# depending on whether the program is hmmsearch, hmmscan, or phmmer
# {hmm,ali}{from,to} can either be hit_{from,to} or query_{from,to}
# for hmmscan, hit is the hmm profile, query is the sequence
if self._meta.get('program') == 'hmmscan':
# adjust 'from' and 'to' coordinates to 0-based ones
frag.hit_start = int(parsed[6]) - 1
frag.hit_end = int(parsed[7])
frag.query_start = int(parsed[9]) - 1
frag.query_end = int(parsed[10])
elif self._meta.get('program') in ['hmmsearch', 'phmmer']:
# adjust 'from' and 'to' coordinates to 0-based ones
frag.hit_start = int(parsed[9]) - 1
frag.hit_end = int(parsed[10])
frag.query_start = int(parsed[6]) - 1
frag.query_end = int(parsed[7])
# strand is always 0, since HMMER now only handles protein
frag.hit_strand = frag.query_strand = 0
hsp = HSP([frag])
hsp.domain_index = int(parsed[0])
hsp.is_included = parsed[1] == '!'
hsp.bitscore = float(parsed[2])
hsp.bias = float(parsed[3])
hsp.evalue_cond = float(parsed[4])
hsp.evalue = float(parsed[5])
if self._meta.get('program') == 'hmmscan':
# adjust 'from' and 'to' coordinates to 0-based ones
hsp.hit_endtype = parsed[8]
hsp.query_endtype = parsed[11]
elif self._meta.get('program') in ['hmmsearch', 'phmmer']:
# adjust 'from' and 'to' coordinates to 0-based ones
hsp.hit_endtype = parsed[11]
hsp.query_endtype = parsed[8]
# adjust 'from' and 'to' coordinates to 0-based ones
hsp.env_start = int(parsed[12]) - 1
hsp.env_end = int(parsed[13])
hsp.env_endtype = parsed[14]
hsp.acc_avg = float(parsed[15])
hsp_list.append(hsp)
self.line = read_forward(self.handle)
# parse the hsp alignments
if self.line.startswith(' Alignments for each domain:'):
self._parse_aln_block(hid, hit.hsps)