def export_naiveseqs_stat(gene, sequences):
result = []
for sequence in sequences:
result.append({
'Accession': sequence['Accession'],
'PMID': sequence['PubMedID'],
'Gene': gene,
'Subtype': sequence['Subtype'],
'NumAAChanges': len(sequence['Mutations']),
'NumInsertions': sequence['NumInsertions'],
'NumDeletions': sequence['NumDeletions'],
'NumStopCodons': sequence['NumStopCodons'],
'NumApobecs': sequence['NumApobecs'],
'NumUnusuals': sequence['NumUnusuals'],
'NumFrameShifts': sequence['NumFrameShifts'],
})
csv_writer(
os.path.join(ROOT, 'data', 'naiveStudies',
'{}StatBySeq.csv'.format(gene)), result,
[
'Accession', 'PMID', 'Gene', 'Subtype', 'NumAAChanges',
'NumInsertions', 'NumDeletions', 'NumStopCodons', 'NumApobecs',
'NumUnusuals', 'NumFrameShifts'
])
def main():
with Pool(max(1, cpu_count() - 2)) as pool:
for gene in ('gag', 'gp41'):
result = calc_distances(gene, pool)
csv_writer(os.path.join(
ROOT, 'local', 'naiveStudies',
'{}NaiveDistance.csv'.format(gene)
), result, ['Sequence1', 'Sequence2', 'Distance'])
def export_unusuals(gene, sequences):
result = []
for seq in sequences:
result.append({
'Accession': seq['Accession'],
'NumUnusuals': seq['NumUnusuals']
})
csv_writer(
os.path.join(ROOT, 'internalFiles', 'naiveStudies',
'{}Unusuals.csv'.format(gene)), result,
['Accession', 'NumUnusuals'])
def export_aa_prevalence(gene, ptseqs):
major_subtypes = [None] + get_most_common_subtypes(gene)
header = ['Gene', 'Subtype', 'Pos', 'AA', 'Pcnt', 'Count', 'PosTotal']
all_prevalence = []
for subtype in major_subtypes:
prevs = aggregate_aa_prevalence(gene, ptseqs, subtype).values()
all_prevalence.append(prevs)
csv_writer(
os.path.join(ROOT, 'data',
'naiveStudies', '{}AAPrevalence.csv'.format(gene)),
chain(*all_prevalence), header)
def export_papers_table(filename, rows):
results = []
for row in rows:
numpt = row['NumLANLIsolatesQCPassed']
if not numpt:
continue
results.append({
'PubMedID': row['PubMedID'],
'PubYear': row['PubYear'],
'NumPatients': numpt,
'RxStatus': row['RxStatus'],
'Title': row['Title'],
'Subtypes': row['Subtypes'],
'Authors': row['Authors'],
})
csv_writer(filename, results, CLEAN_TABLE_HEADERS)
def export_adindex(gene, sequences):
apobecs = {}
for apobec in possible_apobecs_reader(gene):
pos = int(apobec['Position'])
apobecs.setdefault(pos, set()).add(apobec['AAChange'].split('=>',
1)[1])
conserveds = len(apobecs)
result = []
for sequence in sequences:
num_apobecs = sequence['NumApobecs']
index = num_apobecs / conserveds
result.append({
'Accession': sequence['Accession'],
'NumAPOBECs': num_apobecs,
'NumConservedAPOBECSites': conserveds,
'ADIndex': index # APOBEC-mediated defectives index
})
csv_writer(
os.path.join(ROOT, 'internalFiles', 'naiveStudies', 'apobec',
'{}NaiveADIndex.csv'.format(gene)), result,
['Accession', 'NumAPOBECs', 'NumConservedAPOBECSites', 'ADIndex'])
def main():
def cc_keyfunc(c):
return int(c['PID']), c['Rx'], c['Pos']
for gene in ('gag', 'gp41'):
csv_writer(
os.path.join(ROOT, 'internalFiles', 'aaChangesByPosWPrev',
'{}.csv'.format(gene)),
chain(
aggregate_aa_changes_by_pos(gene, 'PIs', 'PIs'),
aggregate_aa_changes_by_pos(gene, 'NNRTIs', 'NNRTIs'),
),
['Group', 'Pos', 'PreAA', 'PostAA',
'NumPts', 'PrePrev', 'PostPrev', 'Fold', 'LogFold'])
csv_writer(
os.path.join(ROOT, 'internalFiles', 'codonChangesByPt',
'{}.csv'.format(gene)),
sorted(
codon_changes_per_person(gene, ('PIs', 'NNRTIs')),
key=cc_keyfunc),
['PID', 'Rx', 'Pos', 'Type', 'Codons', 'NumNAChanges', 'AAs'])
def find_possible_apobecs(gene, ptseqs):
filename = os.path.join(ROOT, 'data', 'naiveStudies', 'apobec',
'{}PossibleApobecs.csv'.format(gene))
apobecs = Counter()
profile = aggregate_aa_prevalence(gene, ptseqs)
for seq in ptseqs:
naseq = seq['AlignedNASequence']
# search for all positions has GG=>AG or GG=>AA change
# deletion gaps should be also considered
matches = re.finditer('A-*(?=[AG])', naseq)
muts = {m['Position']: m for m in seq['Mutations']}
start_codon_apobec_changed = False
if 1 in muts:
first = muts[1]
start_codon_apobec_changed = (first['ReferenceText'] == 'M'
and 'I' in first['AminoAcidText'])
if not start_codon_apobec_changed and not seq['NumStopCodons']:
# no M=>I and no W=>* changes
continue
if seq['NumStopCodons']:
for mut in seq['Mutations']:
if '*' in mut['AminoAcidText']:
cons = mut['ReferenceText']
if cons != 'W':
continue
aa_pos = mut['Position']
cons_prev = profile[(aa_pos, cons)]['Pcnt']
if cons_prev < 97.5:
# skip non-conserved position
continue
apobecs[(aa_pos, 'W=>*')] += 1
for match in matches:
start, end = match.span(0)
# na2 = naseq[end]
aa_pos = start // 3 + 1
na_offset = start % 3
if aa_pos not in muts:
continue
mut = muts[aa_pos]
cons = mut['ReferenceText']
if mut['IsPartial'] or mut['IsInsertion'] or mut['IsDeletion']:
continue
if '*' in mut['AminoAcidText']:
continue
cons_prev = profile[(aa_pos, cons)]['Pcnt']
if cons_prev < 97.5:
# skip non-conserved position
continue
codon = mut['CodonText']
for source in get_codons(cons):
# find G=>A hypermutation
if source[na_offset] != 'G':
continue
target = source[:na_offset] + 'A' + source[na_offset + 1:]
if compare_codon(target, codon):
target_aa = translate_codon(target)
if target_aa == cons:
# do not add things like "E=>E"
break
apobecs[(aa_pos, '{}=>{}'.format(cons, target_aa))] += 1
break
possible_apobecs = []
for (pos, mut), count in apobecs.most_common():
possible_apobecs.append({
'Position':
pos,
'AAChange':
mut,
'Consensus %':
profile[pos, mut.split('=>', 1)[0]]['Pcnt'].quantize(PREC1),
'# with Stop':
count
})
for seq in ptseqs:
muts = {m['Position']: m for m in seq['Mutations']}
for apobec in possible_apobecs:
pos = apobec['Position']
aa = apobec['AAChange'].split('=>', 1)[1]
if pos in muts and aa in muts[pos]['AminoAcidText']:
apobec['# Sequence'] = apobec.get('# Sequence', 0) + 1
for apobec in possible_apobecs:
apobec['% with Stop'] = Decimal(apobec['# with Stop'] * 100 /
apobec['# Sequence']).quantize(PREC0)
possible_apobecs = sorted(possible_apobecs,
key=lambda a: (a['Position'], a['AAChange']))
possible_apobecs = [a for a in possible_apobecs if a['% with Stop'] > 50]
csv_writer(
filename,
possible_apobecs,
['Position', 'AAChange', 'Consensus %', '% with Stop', '# Sequence'],
writer_options={'extrasaction': 'ignore'})
def create_review_table(gene, ptseqs):
fact_table = get_fact_table(gene)
grouped = groupby(ptseqs, lambda s: s['_PubID'])
results = {}
for pubid, group_seqs in grouped:
group_seqs = list(group_seqs)
subtypes = sorted({s['Subtype'] for s in group_seqs})
seq = group_seqs[0]
fact = fact_table.get(pubid, {})
if fact.get('PubIDCorrection'):
pubid = fact['PubIDCorrection']
if pubid not in results:
results[pubid] = {
'PubID':
pubid,
'PubMedID':
fact.get('PMID') or seq['PubMedID'],
'PubYear':
fact.get('PubYr') or seq['PubYear'],
'NumPts':
fact.get('NumPts'),
'NumIsolates':
fact.get('NumIsolates'),
'NumLANLIsolates':
len(group_seqs),
'NumLANLIsolatesQCPassed':
len([s for s in group_seqs if s['Included']]),
'Title':
seq['Title'],
'Authors':
seq['Authors'],
'Subtypes':
'; '.join(subtypes),
'RxStatus':
fact.get('RxStatus'),
'Notes':
fact.get('Notes'),
}
else:
result = results[pubid]
origsubtypes = result['Subtypes'].split('; ')
subtypes = sorted(set(origsubtypes + subtypes))
result['Subtypes'] = '; '.join(subtypes)
if not result.get('PubYear'):
result['PubYear'] = fact.get('PubYr') or seq['PubYear']
if not result.get('PubMedID'):
result['PubMedID'] = fact.get('PMID') or seq['PubMedID']
num_pts = int(result['NumPts'] or 0)
num_pts += int(fact.get('NumPts') or 0)
if num_pts:
result['NumPts'] = str(num_pts)
num_isos = int(result['NumIsolates'] or 0)
num_isos += int(fact.get('NumIsolates') or 0)
if num_isos:
result['NumIsolates'] = str(num_isos)
result['NumLANLIsolates'] += len(group_seqs)
result['NumLANLIsolatesQCPassed'] += len(
[s for s in group_seqs if s['Included']])
if not result.get('RxStatus'):
result['RxStatus'] = fact.get('RxStatus')
results = sorted(results.values(),
key=lambda r: (-r['NumLANLIsolates'], r['PubID']))
csv_writer(
os.path.join(ROOT, 'internalFiles', 'papersReview',
'{}ReviewTable.csv'.format(gene)), results,
REVIEW_TABLE_HEADERS)
export_excel_table(
os.path.join(ROOT, 'internalFiles', 'papersReview',
'{}ReviewTable.xlsx'.format(gene)), results)
export_papers_table(
os.path.join(ROOT, 'data', 'naiveStudies',
'{}Studies.csv'.format(gene)), results)
def export_naive_sequences(gene, ptseqs):
filename = os.path.join(ROOT, 'internalFiles', 'naiveStudies',
'{}.csv'.format(gene.lower()))
aligned_fasta = os.path.join(ROOT, 'data', 'naiveStudies',
'{}NaiveAligned.fas'.format(gene.lower()))
unaligned_fasta = os.path.join(ROOT, 'data', 'naiveStudies',
'{}NaiveOriginal.fas'.format(gene.lower()))
indels_csv = os.path.join(ROOT, 'data', 'naiveStudies',
'{}NaiveIndels.csv'.format(gene.lower()))
genesize = int(CONSENSUS[gene]['Size'])
siteheaders = ['P{}'.format(i) for i in range(1, genesize + 1)]
rows = []
indels = []
ptseqs = sorted(ptseqs, key=lambda s: s['Accession'])
for seq in ptseqs:
firstaa = seq['FirstAA']
lastaa = seq['LastAA']
muts = {m['Position']: m for m in seq['Mutations']}
row = {
'PMID': seq['PubMedID'],
'Accession': seq['Accession'],
'RxStatus': 'Naive',
'lanlSubtype': seq['Subtype'],
'NumAAChanges': len(muts),
'NumInsertions': seq['NumInsertions'],
'NumDeletions': seq['NumDeletions'],
'NumStopCodons': seq['NumStopCodons'],
'NumApobecs': seq['NumApobecs'],
'NumUnusuals': seq['NumUnusuals'],
'NumFrameShifts': seq['NumFrameShifts']
}
for pos in range(1, genesize + 1):
pname = 'P{}'.format(pos)
if pos < firstaa or pos > lastaa:
row[pname] = '.'
elif pos not in muts:
row[pname] = '-'
else:
mut = muts[pos]
if mut['IsInsertion']:
row[pname] = 'i'
elif mut['IsDeletion']:
row[pname] = 'd'
elif mut['IsPartial']:
row[pname] = 'X'
else:
aas = mut['AminoAcidText']
if len(aas) > 4:
aas = 'X'
row[pname] = aas
rows.append(row)
for mut in seq['Mutations']:
if mut['IsPartial'] or not (mut['IsInsertion']
or mut['IsDeletion']):
continue
isins = mut['IsInsertion']
indels.append({
'Accession':
seq['Accession'],
'Gene':
gene,
'Position':
mut['Position'],
'IndelType':
'ins' if isins else 'del',
'Codon':
mut['CodonText'] if isins else '',
'InsertedCodons':
mut['InsertedCodonsText'] if isins else ''
})
csv_writer(filename, rows, [
'PMID', 'Accession', 'RxStatus', 'lanlSubtype', 'NumAAChanges',
'NumInsertions', 'NumDeletions', 'NumStopCodons', 'NumApobecs',
'NumUnusuals', 'NumFrameShifts'
] + siteheaders)
csv_writer(indels_csv, indels, [
'Accession', 'Gene', 'Position', 'IndelType', 'Codon', 'InsertedCodons'
])
data_writer(
aligned_fasta,
'\n'.join('>{Accession}|{Subtype}\n{AlignedNASequence}'.format(**s)
for s in ptseqs))
data_writer(
unaligned_fasta,
'\n'.join('>{Accession}|{Subtype}\n{NASequence}'.format(**s)
for s in ptseqs))
print('- {} naive {} sequences were exported'.format(len(ptseqs), gene))
