def get_pos_in_alignment(codon, aligned_seq, seq, pos):
""" given <pos> in <seq>, find the codon's position in <aligned_seq> """
assert utils.codon_ok(
codon, seq, pos, debug=debug
) # this only gets called on the gene with the *known* position, so it shouldn't fail
pos_in_alignment = pos + get_n_gaps_up_to_pos(aligned_seq, pos)
assert utils.codon_ok(codon, aligned_seq, pos_in_alignment, debug=debug)
return pos_in_alignment
def generate_snpd_gene(gene, cpos, seq, positions):
assert utils.get_region(gene) == "v" # others not yet handled
def choose_position():
snp_pos = None
while snp_pos is None or snp_pos in snpd_positions or not utils.codon_ok("cyst", tmpseq, cpos, debug=True):
snp_pos = random.randint(10, len(seq) - 15) # note that randint() is inclusive
tmpseq = seq[:snp_pos] + "X" + seq[snp_pos + 1 :] # for checking cyst position
return snp_pos
snpd_positions = set() # only used if a position wasn't specified (i.e. was None) in <snps_to_add>
mutfo = OrderedDict()
for snp_pos in positions:
if snp_pos is None:
snp_pos = choose_position()
snpd_positions.add(snp_pos)
new_base = None
while new_base is None or new_base == seq[snp_pos]:
new_base = utils.nukes[random.randint(0, len(utils.nukes) - 1)]
print " %3d %s --> %s" % (snp_pos, seq[snp_pos], new_base)
mutfo[snp_pos] = {"original": seq[snp_pos], "new": new_base}
seq = seq[:snp_pos] + new_base + seq[snp_pos + 1 :]
assert utils.codon_ok("cyst", seq, cpos, debug=True) # this is probably unnecessary
snpd_name, mutfo = get_new_allele_name_and_change_mutfo(gene, mutfo)
return {"template-gene": gene, "gene": snpd_name, "seq": seq}
def revert_conserved_codons(self, seq):
""" revert conserved cysteine and tryptophan to their original bases, eg if they were messed up by s.h.m. """
for region, pos in self.final_codon_positions.items():
if seq[pos : pos + 3] != self.unmutated_codons[region]:
assert len(self.unmutated_codons[region]) == 3
seq = seq[:pos] + self.unmutated_codons[region] + seq[pos + 3 :]
assert utils.codon_ok(utils.conserved_codons[self.glfo['chain']][region], seq, pos)
return seq
def remove_v_genes_with_bad_cysteines(glfo, debug=False):
prelength = len(glfo["seqs"]["v"])
for gene in glfo["seqs"]["v"].keys():
# if len(glfo['seqs']['v'][gene]) < glfo['cyst-positions'][gene] + 3:
if not utils.codon_ok("cyst", glfo["seqs"]["v"][gene], glfo["cyst-positions"][gene]):
remove_gene(glfo, gene, debug=debug)
if True: # debug:
print " removed %d / %d v genes with bad cysteines" % (
prelength - len(glfo["seqs"]["v"]),
len(glfo["seqs"]["v"]),
)
def choose_position():
snp_pos = None
while snp_pos is None or snp_pos in snpd_positions or not utils.codon_ok("cyst", tmpseq, cpos, debug=True):
snp_pos = random.randint(10, len(seq) - 15) # note that randint() is inclusive
tmpseq = seq[:snp_pos] + "X" + seq[snp_pos + 1 :] # for checking cyst position
return snp_pos
def get_missing_codon_info(glfo, debug=False):
# ----------------------------------------------------------------------------------------
def get_n_gaps_up_to_pos(aligned_seq, pos):
# NOTE I think this duplicates the functionality of count_gaps()
""" return number of gapped positions in <aligned_seq> before <pos> """
ipos = 0 # position in unaligned sequence
n_gaps_passed = (
0
) # number of gapped positions in the aligned sequence that we pass before getting to <pos> (i.e. while ipos < pos)
while ipos < pos:
if aligned_seq[ipos + n_gaps_passed] in utils.gap_chars:
n_gaps_passed += 1
else:
ipos += 1
return n_gaps_passed
# ----------------------------------------------------------------------------------------
def get_pos_in_alignment(codon, aligned_seq, seq, pos):
""" given <pos> in <seq>, find the codon's position in <aligned_seq> """
assert utils.codon_ok(
codon, seq, pos, debug=debug
) # this only gets called on the gene with the *known* position, so it shouldn't fail
pos_in_alignment = pos + get_n_gaps_up_to_pos(aligned_seq, pos)
assert utils.codon_ok(codon, aligned_seq, pos_in_alignment, debug=debug)
return pos_in_alignment
for region, codon in utils.conserved_codons[glfo["chain"]].items():
missing_genes = set(glfo["seqs"][region]) - set(glfo[codon + "-positions"])
if len(missing_genes) == 0:
if debug:
print " no missing %s info" % codon
continue
if debug:
print " missing %d %s positions" % (len(missing_genes), codon)
aligned_seqs = get_new_alignments(glfo, region, debug=debug)
# for g, s in aligned_seqs.items():
# print s, utils.color_gene(g)
# if region == 'j':
# raise Exception('missing tryp position for %s, and we can\'t infer it because tryp positions don\'t reliably align to the same position' % ' '.join(missing_genes))
# existing codon position (this assumes that once aligned, all genes have the same codon position -- which is only really true for the imgt-gapped alignment)
if len(glfo[codon + "-positions"]) > 0:
known_gene, known_pos = None, None
for gene, pos in glfo[
codon + "-positions"
].items(): # take the first one for which we have the sequence (NOTE it would be safer to check that they're all the same)
if (
gene in glfo["seqs"][region]
and gene in aligned_seqs
and utils.codon_ok(codon, glfo["seqs"][region][gene], pos)
):
known_gene, known_pos = gene, pos
break
if known_gene is None:
raise Exception("couldn't find a known %s position" % codon)
# NOTE for cyst, should be 309 if alignments are imgt [which they used to usually be, but now probably aren't] (imgt says 104th codon --> subtract 1 to get zero-indexing, then multiply by three 3 * (104 - 1) = 309
known_pos_in_alignment = get_pos_in_alignment(
codon, aligned_seqs[known_gene], glfo["seqs"][region][known_gene], known_pos
)
if debug:
print " using known position %d (aligned %d) in %s" % (
known_pos,
known_pos_in_alignment,
known_gene,
)
elif codon == "cyst":
known_pos_in_alignment = 309
print " assuming aligned %s position is %d (this will %s work if you're using imgt alignments)" % (
codon,
known_pos_in_alignment,
utils.color("red", "only"),
)
raise Exception("not really using imgt alignments much any more, so this isn't really going to work")
else:
raise Exception("no existing %s info, and couldn't guess it, either" % codon)
n_added = 0
seqons = [] # (seq, pos) pairs
for gene in missing_genes:
unaligned_pos = known_pos_in_alignment - utils.count_gaps(aligned_seqs[gene], istop=known_pos_in_alignment)
seq_to_check = glfo["seqs"][region][gene]
seqons.append((seq_to_check, unaligned_pos))
glfo[codon + "-positions"][gene] = unaligned_pos
n_added += 1
# if debug:
# tmpseq = aligned_seqs[gene]
# tmppos = known_pos_in_alignment
# print ' %s%s%s %s (new)' % (tmpseq[:tmppos], utils.color('reverse_video', tmpseq[tmppos : tmppos + 3]), tmpseq[tmppos + 3:], utils.color_gene(gene))
utils.check_a_bunch_of_codons(codon, seqons, extra_str=" ", debug=debug)
if debug:
print " added %d %s positions" % (n_added, codon)
