Mercurial > repos > cpt > cpt_find_spanins
view cpt.py @ 0:9708448ce811 draft
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author | cpt |
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date | Fri, 17 Jun 2022 12:39:30 +0000 |
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children | 46b252c89e9e |
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#!/usr/bin/env python from Bio.Seq import Seq, reverse_complement, translate from Bio.SeqRecord import SeqRecord from Bio import SeqIO from Bio.Data import CodonTable import logging logging.basicConfig() log = logging.getLogger() PHAGE_IN_MIDDLE = re.compile("^(?P<host>.*)\s*phage (?P<phage>.*)$") BACTERIOPHAGE_IN_MIDDLE = re.compile("^(?P<host>.*)\s*bacteriophage (?P<phage>.*)$") STARTS_WITH_PHAGE = re.compile( "^(bacterio|vibrio|Bacterio|Vibrio|)?[Pp]hage (?P<phage>.*)$" ) NEW_STYLE_NAMES = re.compile("(?P<phage>v[A-Z]_[A-Z][a-z]{2}_.*)") def phage_name_parser(name): host = None phage = None name = name.replace(", complete genome.", "") name = name.replace(", complete genome", "") m = BACTERIOPHAGE_IN_MIDDLE.match(name) if m: host = m.group("host") phage = m.group("phage") return (host, phage) m = PHAGE_IN_MIDDLE.match(name) if m: host = m.group("host") phage = m.group("phage") return (host, phage) m = STARTS_WITH_PHAGE.match(name) if m: phage = m.group("phage") return (host, phage) m = NEW_STYLE_NAMES.match(name) if m: phage = m.group("phage") return (host, phage) return (host, phage) class OrfFinder(object): def __init__(self, table, ftype, ends, min_len, strand): self.table = table self.table_obj = CodonTable.ambiguous_generic_by_id[table] self.ends = ends self.ftype = ftype self.min_len = min_len self.starts = sorted(self.table_obj.start_codons) self.stops = sorted(self.table_obj.stop_codons) self.re_starts = re.compile("|".join(self.starts)) self.re_stops = re.compile("|".join(self.stops)) self.strand = strand def locate(self, fasta_file, out_nuc, out_prot, out_bed, out_gff3): seq_format = "fasta" log.debug("Genetic code table %i" % self.table) log.debug("Minimum length %i aa" % self.min_len) out_count = 0 out_gff3.write("##gff-version 3\n") for idx, record in enumerate(SeqIO.parse(fasta_file, seq_format)): for i, (f_start, f_end, f_strand, n, t) in enumerate( self.get_all_peptides(str(record.seq).upper()) ): out_count += 1 descr = "length %i aa, %i bp, from %s..%s[%s] of %s" % ( len(t), len(n), f_start, f_end, f_strand, record.description, ) fid = record.id + "|%s%i" % (self.ftype, i + 1) r = SeqRecord(Seq(n), id=fid, name="", description=descr) t = SeqRecord(Seq(t), id=fid, name="", description=descr) SeqIO.write(r, out_nuc, "fasta") SeqIO.write(t, out_prot, "fasta") nice_strand = "+" if f_strand == +1 else "-" out_bed.write( "\t".join( map(str, [record.id, f_start, f_end, fid, 0, nice_strand]) ) + "\n" ) out_gff3.write( "\t".join( map( str, [ record.id, "getOrfsOrCds", "CDS", f_start + 1, f_end, ".", nice_strand, 0, "ID=%s.%s.%s" % (self.ftype, idx, i + 1), ], ) ) + "\n" ) log.info("Found %i %ss", out_count, self.ftype) def start_chop_and_trans(self, s, strict=True): """Returns offset, trimmed nuc, protein.""" if strict: assert s[-3:] in self.stops, s assert len(s) % 3 == 0 for match in self.re_starts.finditer(s, overlapped=True): # Must check the start is in frame start = match.start() if start % 3 == 0: n = s[start:] assert len(n) % 3 == 0, "%s is len %i" % (n, len(n)) if strict: t = translate(n, self.table) else: # Use when missing stop codon, t = "M" + translate(n[3:], self.table, to_stop=True) yield start, n, t # Edited by CPT to be a generator def break_up_frame(self, s): """Returns offset, nuc, protein.""" start = 0 for match in self.re_stops.finditer(s, overlapped=True): index = match.start() + 3 if index % 3 != 0: continue n = s[start:index] for (offset, n, t) in self.start_chop_and_trans(n): if n and len(t) >= self.min_len: yield start + offset, n, t start = index def putative_genes_in_sequence(self, nuc_seq): """Returns start, end, strand, nucleotides, protein. Co-ordinates are Python style zero-based. """ nuc_seq = nuc_seq.upper() # TODO - Refactor to use a generator function (in start order) # rather than making a list and sorting? answer = [] full_len = len(nuc_seq) for frame in range(0, 3): for offset, n, t in self.break_up_frame(nuc_seq[frame:]): start = frame + offset # zero based answer.append((start, start + len(n), +1, n, t)) rc = reverse_complement(nuc_seq) for frame in range(0, 3): for offset, n, t in self.break_up_frame(rc[frame:]): start = full_len - frame - offset # zero based answer.append((start, start - len(n), -1, n, t)) answer.sort() return answer def get_all_peptides(self, nuc_seq): """Returns start, end, strand, nucleotides, protein. Co-ordinates are Python style zero-based. """ # Refactored into generator by CPT full_len = len(nuc_seq) if self.strand != "reverse": for frame in range(0, 3): for offset, n, t in self.break_up_frame(nuc_seq[frame:]): start = frame + offset # zero based yield (start, start + len(n), +1, n, t) if self.strand != "forward": rc = reverse_complement(nuc_seq) for frame in range(0, 3): for offset, n, t in self.break_up_frame(rc[frame:]): start = full_len - frame - offset # zero based yield (start - len(n), start, -1, n, t) class MGAFinder(object): def __init__(self, table, ftype, ends, min_len): self.table = table self.table_obj = CodonTable.ambiguous_generic_by_id[table] self.ends = ends self.ftype = ftype self.min_len = min_len self.starts = sorted(self.table_obj.start_codons) self.stops = sorted(self.table_obj.stop_codons) self.re_starts = re.compile("|".join(self.starts)) self.re_stops = re.compile("|".join(self.stops)) def locate(self, fasta_file, out_nuc, out_prot, out_bed, out_gff3): seq_format = "fasta" log.debug("Genetic code table %i" % self.table) log.debug("Minimum length %i aa" % self.min_len) out_count = 0 out_gff3.write("##gff-version 3\n") for idx, record in enumerate(SeqIO.parse(fasta_file, seq_format)): for i, (f_start, f_end, f_strand, n, t) in enumerate( self.get_all_peptides(str(record.seq).upper()) ): out_count += 1 descr = "length %i aa, %i bp, from %s..%s[%s] of %s" % ( len(t), len(n), f_start, f_end, f_strand, record.description, ) fid = record.id + "|%s%i" % (self.ftype, i + 1) r = SeqRecord(Seq(n), id=fid, name="", description=descr) t = SeqRecord(Seq(t), id=fid, name="", description=descr) SeqIO.write(r, out_nuc, "fasta") SeqIO.write(t, out_prot, "fasta") nice_strand = "+" if f_strand == +1 else "-" out_bed.write( "\t".join( map(str, [record.id, f_start, f_end, fid, 0, nice_strand]) ) + "\n" ) out_gff3.write( "\t".join( map( str, [ record.id, "getOrfsOrCds", "CDS", f_start + 1, f_end, ".", nice_strand, 0, "ID=%s.%s.%s" % (self.ftype, idx, i + 1), ], ) ) + "\n" ) log.info("Found %i %ss", out_count, self.ftype) def start_chop_and_trans(self, s, strict=True): """Returns offset, trimmed nuc, protein.""" if strict: assert s[-3:] in self.stops, s assert len(s) % 3 == 0 for match in self.re_starts.finditer(s, overlapped=True): # Must check the start is in frame start = match.start() if start % 3 == 0: n = s[start:] assert len(n) % 3 == 0, "%s is len %i" % (n, len(n)) if strict: t = translate(n, self.table) else: # Use when missing stop codon, t = "M" + translate(n[3:], self.table, to_stop=True) yield start, n, t def break_up_frame(self, s): """Returns offset, nuc, protein.""" start = 0 for match in self.re_stops.finditer(s, overlapped=True): index = match.start() + 3 if index % 3 != 0: continue n = s[start:index] for (offset, n, t) in self.start_chop_and_trans(n): if n and len(t) >= self.min_len: yield start + offset, n, t start = index def putative_genes_in_sequence(self, nuc_seq): """Returns start, end, strand, nucleotides, protein. Co-ordinates are Python style zero-based. """ nuc_seq = nuc_seq.upper() # TODO - Refactor to use a generator function (in start order) # rather than making a list and sorting? answer = [] full_len = len(nuc_seq) for frame in range(0, 3): for offset, n, t in self.break_up_frame(nuc_seq[frame:]): start = frame + offset # zero based answer.append((start, start + len(n), +1, n, t)) rc = reverse_complement(nuc_seq) for frame in range(0, 3): for offset, n, t in self.break_up_frame(rc[frame:]): start = full_len - frame - offset # zero based answer.append((start, start - len(n), -1, n, t)) answer.sort() return answer def get_all_peptides(self, nuc_seq): """Returns start, end, strand, nucleotides, protein. Co-ordinates are Python style zero-based. """ # Refactored into generator by CPT full_len = len(nuc_seq) for frame in range(0, 3): for offset, n, t in self.break_up_frame(nuc_seq[frame:]): start = frame + offset # zero based yield (start, start + len(n), +1, n, t) rc = reverse_complement(nuc_seq) for frame in range(0, 3): for offset, n, t in self.break_up_frame(rc[frame:]): start = full_len - frame - offset # zero based yield (start - len(n), start, -1, n, t)