Mercurial > repos > earlhaminst > gstf_preparation
view gstf_preparation.py @ 13:51a7a2a82902 draft
"planemo upload for repository https://github.com/TGAC/earlham-galaxytools/tree/master/tools/gstf_preparation commit 9178f870760132962f8d3a26ea55c201880bb018-dirty"
author | earlhaminst |
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date | Tue, 06 Oct 2020 17:10:37 +0000 |
parents | 99bae410128c |
children | 598e9172b8e7 |
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import json import optparse import os import sqlite3 import sys version = "0.5.0" gene_count = 0 def asbool(val): if isinstance(val, str): val_lower = val.strip().lower() if val_lower in ('true', '1'): return True elif val_lower in ('false', '0'): return False else: raise ValueError(f"Cannot convert {val} to bool") else: return bool(val) class Sequence: def __init__(self, header, sequence_parts): self.header = header self.sequence_parts = sequence_parts self._sequence = None @property def sequence(self): if self._sequence is None: self._sequence = ''.join(self.sequence_parts) return self._sequence def print(self, fh=sys.stdout): print(self.header, file=fh) for line in self.sequence_parts: print(line, file=fh) def FASTAReader_gen(fasta_filename): with open(fasta_filename) as fasta_file: line = fasta_file.readline() while True: if not line: return assert line.startswith('>'), "FASTA headers must start with >" header = line.rstrip() sequence_parts = [] line = fasta_file.readline() while line and line[0] != '>': sequence_parts.append(line.rstrip()) line = fasta_file.readline() yield Sequence(header, sequence_parts) def create_tables(conn): cur = conn.cursor() cur.execute('''CREATE TABLE meta ( version VARCHAR PRIMARY KEY NOT NULL)''') cur.execute('INSERT INTO meta (version) VALUES (?)', (version, )) cur.execute('''CREATE TABLE gene ( gene_id VARCHAR PRIMARY KEY NOT NULL, gene_symbol VARCHAR, seq_region_name VARCHAR NOT NULL, seq_region_start INTEGER NOT NULL, seq_region_end INTEGER NOT NULL, seq_region_strand INTEGER NOT NULL, species VARCHAR NOT NULL, biotype VARCHAR, gene_json VARCHAR NOT NULL)''') cur.execute('CREATE INDEX gene_symbol_index ON gene (gene_symbol)') cur.execute('''CREATE TABLE transcript ( transcript_id VARCHAR PRIMARY KEY NOT NULL, transcript_symbol VARCHAR, protein_id VARCHAR UNIQUE, protein_sequence VARCHAR, biotype VARCHAR, is_canonical BOOLEAN NOT NULL DEFAULT FALSE, gene_id VARCHAR NOT NULL REFERENCES gene(gene_id))''') # The following temporary view is not used in GAFA, so schema changes to it # don't require a meta version upgrade. cur.execute('''CREATE TEMPORARY VIEW transcript_join_gene AS SELECT transcript_id, transcript_symbol, COALESCE(transcript.biotype, gene.biotype) AS biotype, is_canonical, gene_id, gene_symbol, seq_region_name, species FROM transcript JOIN gene USING (gene_id)''') conn.commit() def fetch_transcript_and_gene(conn, transcript_id): cur = conn.cursor() cur.execute('SELECT * FROM transcript_join_gene WHERE transcript_id=?', (transcript_id, )) return cur.fetchone() def remove_type_from_list_of_ids(ids): return ','.join(remove_type_from_id(id_) for id_ in ids.split(',')) def remove_type_from_id(id_): colon_index = id_.find(':') if colon_index >= 0: return id_[colon_index + 1:] else: return id_ def feature_to_dict(cols, parent_dict=None): d = { 'end': int(cols[4]), 'start': int(cols[3]), } for attr in cols[8].split(';'): if '=' in attr: (tag, value) = attr.split('=') if tag == 'ID': tag = 'id' value = remove_type_from_id(value) elif tag == 'Parent': value = remove_type_from_list_of_ids(value) elif tag == 'representative': tag = 'is_canonical' d[tag] = value if cols[6] == '+': d['strand'] = 1 elif cols[6] == '-': d['strand'] = -1 else: raise Exception("Unrecognized strand '%s'" % cols[6]) if parent_dict is not None and 'Parent' in d: # a 3' UTR can be split among multiple exons # a 5' UTR can be split among multiple exons # a CDS can be part of multiple transcripts for parent in d['Parent'].split(','): parent_dict.setdefault(parent, []).append(d) return d def add_gene_to_dict(cols, species, gene_dict): global gene_count gene = feature_to_dict(cols) if not gene['id']: raise Exception("Id not found among column 9 attribute tags: %s" % cols[8]) gene.update({ 'member_id': gene_count, 'object_type': 'Gene', 'seq_region_name': cols[0], 'species': species, 'Transcript': [], 'display_name': gene.get('Name'), }) gene_dict[gene['id']] = gene gene_count = gene_count + 1 def add_transcript_to_dict(cols, species, transcript_dict): transcript = feature_to_dict(cols) transcript.update({ 'object_type': 'Transcript', 'seq_region_name': cols[0], 'species': species, 'display_name': transcript.get('Name'), }) transcript_dict[transcript['id']] = transcript def add_exon_to_dict(cols, species, exon_parent_dict): exon = feature_to_dict(cols, exon_parent_dict) exon.update({ 'length': int(cols[4]) - int(cols[3]) + 1, 'object_type': 'Exon', 'seq_region_name': cols[0], 'species': species, }) if 'id' not in exon and 'Name' in exon: exon['id'] = exon['Name'] def add_cds_to_dict(cols, cds_parent_dict): cds = feature_to_dict(cols, cds_parent_dict) if 'id' not in cds: if 'Name' in cds: cds['id'] = cds['Name'] elif 'Parent' in cds and ',' not in cds['Parent']: cds['id'] = cds['Parent'] def join_dicts(gene_dict, transcript_dict, exon_parent_dict, cds_parent_dict, five_prime_utr_parent_dict, three_prime_utr_parent_dict): for parent, exon_list in exon_parent_dict.items(): if parent in transcript_dict: exon_list.sort(key=lambda _: _['start']) transcript_dict[parent]['Exon'] = exon_list for transcript_id, transcript in transcript_dict.items(): translation = { 'CDS': [], 'id': None, 'end': transcript['end'], 'object_type': 'Translation', 'species': transcript['species'], 'start': transcript['start'], } found_cds = False derived_translation_start = None derived_translation_end = None if transcript_id in cds_parent_dict: cds_list = cds_parent_dict[transcript_id] cds_ids = {_['id'] for _ in cds_list} if len(cds_ids) > 1: raise Exception("Transcript %s has multiple CDSs: this is not supported by Ensembl JSON format" % transcript_id) cds_id = cds_ids.pop() translation['id'] = cds_id cds_list.sort(key=lambda _: _['start']) translation['CDS'] = cds_list translation['start'] = cds_list[0]['start'] translation['end'] = cds_list[-1]['end'] found_cds = True if transcript_id in five_prime_utr_parent_dict: five_prime_utr_list = five_prime_utr_parent_dict[transcript_id] five_prime_utr_list.sort(key=lambda _: _['start']) if transcript['strand'] == 1: derived_translation_start = five_prime_utr_list[-1]['end'] + 1 else: derived_translation_end = five_prime_utr_list[0]['start'] - 1 if transcript_id in three_prime_utr_parent_dict: three_prime_utr_list = three_prime_utr_parent_dict[transcript_id] three_prime_utr_list.sort(key=lambda _: _['start']) if transcript['strand'] == 1: derived_translation_end = three_prime_utr_list[0]['start'] - 1 else: derived_translation_start = three_prime_utr_list[-1]['end'] + 1 if derived_translation_start is not None: if found_cds: if derived_translation_start > translation['start']: raise Exception(f"Transcript {transcript_id} has the start of CDS {cds_id} overlapping with the UTR end") else: translation['start'] = derived_translation_start if derived_translation_end is not None: if found_cds: if derived_translation_end < translation['end']: raise Exception(f"Transcript {transcript_id} has the end of CDS {cds_id} overlapping with the UTR start") else: translation['end'] = derived_translation_end if found_cds or derived_translation_start is not None or derived_translation_end is not None: transcript['Translation'] = translation for transcript in transcript_dict.values(): if 'Parent' in transcript: # A polycistronic transcript can have multiple parents for parent in transcript['Parent'].split(','): if parent in gene_dict: gene_dict[parent]['Transcript'].append(transcript) def write_gene_dict_to_db(conn, gene_dict): cur = conn.cursor() for gene in gene_dict.values(): if gene is None: # This can happen when loading a JSON file from Ensembl continue if 'confidence' in gene and gene['confidence'].lower() != 'high': print("Gene {} has confidence {} (not high), discarding".format(gene['id'], gene['confidence']), file=sys.stderr) continue gene_id = gene['id'] cur.execute('INSERT INTO gene (gene_id, gene_symbol, seq_region_name, seq_region_start, seq_region_end, seq_region_strand, species, biotype, gene_json) VALUES (?, ?, ?, ?, ?, ?, ?, ?, ?)', (gene_id, gene.get('display_name'), gene['seq_region_name'], gene['start'], gene['end'], gene['strand'], gene['species'], gene.get('biotype'), json.dumps(gene))) if "Transcript" in gene: for transcript in gene["Transcript"]: transcript_id = transcript['id'] transcript_symbol = transcript.get('display_name') protein_id = transcript.get('Translation', {}).get('id') biotype = transcript.get('biotype') is_canonical = asbool(transcript.get('is_canonical', False)) to_insert = (transcript_id, transcript_symbol, protein_id, biotype, is_canonical, gene_id) try: cur.execute('INSERT INTO transcript (transcript_id, transcript_symbol, protein_id, biotype, is_canonical, gene_id) VALUES (?, ?, ?, ?, ?, ?)', to_insert) except Exception as e: raise Exception("Error while inserting {} into transcript table: {}".format(str(to_insert), e)) conn.commit() def remove_id_version(s, force=False): """ Remove the optional '.VERSION' from an id if it's an Ensembl id or if `force` is True. """ if force or s.startswith('ENS'): return s.split('.')[0] else: return s def __main__(): parser = optparse.OptionParser() parser.add_option('--gff3', action='append', default=[], help='GFF3 file to convert, in SPECIES:FILENAME format. Use multiple times to add more files') parser.add_option('--json', action='append', default=[], help='JSON file to merge. Use multiple times to add more files') parser.add_option('--fasta', action='append', default=[], help='Path of the input FASTA files') parser.add_option('--filter', type='choice', choices=['canonical', 'coding', ''], default='', help='Which transcripts to keep') parser.add_option('--headers', type='choice', choices=['TranscriptId_species', 'TranscriptID-GeneSymbol_species', 'TranscriptID-TranscriptSymbol_species', ''], default='', help='Change the header line of the FASTA sequences to this format') parser.add_option('--regions', default="", help='Comma-separated list of region IDs for which FASTA sequences should be filtered') parser.add_option('-o', '--output', help='Path of the output SQLite file') parser.add_option('--of', help='Path of the output FASTA file') parser.add_option('--ff', default=os.devnull, help='Path of the filtered sequences output FASTA file') options, args = parser.parse_args() if args: raise Exception('Use options to provide inputs') conn = sqlite3.connect(options.output) conn.row_factory = sqlite3.Row conn.execute('PRAGMA foreign_keys = ON') create_tables(conn) for gff3_arg in options.gff3: try: (species, filename) = gff3_arg.split(':') except ValueError: raise Exception("Argument for --gff3 '%s' is not in the SPECIES:FILENAME format" % gff3_arg) gene_dict = dict() transcript_dict = dict() exon_parent_dict = dict() cds_parent_dict = dict() five_prime_utr_parent_dict = dict() three_prime_utr_parent_dict = dict() unimplemented_feature_nlines_dict = dict() with open(filename) as f: for i, line in enumerate(f, start=1): line = line.strip() if not line: # skip empty lines continue if line[0] == '#': # skip comment lines continue cols = line.split('\t') if len(cols) != 9: raise Exception("Line %i in file '%s': '%s' does not have 9 columns" % (i, filename, line)) feature_type = cols[2] try: if feature_type == 'gene': add_gene_to_dict(cols, species, gene_dict) elif feature_type in ('mRNA', 'transcript'): add_transcript_to_dict(cols, species, transcript_dict) elif feature_type == 'exon': add_exon_to_dict(cols, species, exon_parent_dict) elif feature_type == 'five_prime_UTR': feature_to_dict(cols, five_prime_utr_parent_dict) elif feature_type == 'three_prime_UTR': feature_to_dict(cols, three_prime_utr_parent_dict) elif feature_type == 'CDS': add_cds_to_dict(cols, cds_parent_dict) elif feature_type in unimplemented_feature_nlines_dict: unimplemented_feature_nlines_dict[feature_type] += 1 else: unimplemented_feature_nlines_dict[feature_type] = 0 except Exception as e: print("Line %i in file '%s': %s" % (i, filename, e), file=sys.stderr) for unimplemented_feature, nlines in unimplemented_feature_nlines_dict.items(): print("Skipped %d lines in GFF3 file '%s': '%s' is not an implemented feature type" % (nlines, filename, unimplemented_feature), file=sys.stderr) join_dicts(gene_dict, transcript_dict, exon_parent_dict, cds_parent_dict, five_prime_utr_parent_dict, three_prime_utr_parent_dict) write_gene_dict_to_db(conn, gene_dict) for json_arg in options.json: with open(json_arg) as f: write_gene_dict_to_db(conn, json.load(f)) # Read the FASTA files a first time to: # - determine for each file if we need to force the removal of the version # from the transcript id # - fill gene_transcripts_dict when keeping only the canonical transcripts force_remove_id_version_file_list = [] gene_transcripts_dict = dict() for fasta_arg in options.fasta: force_remove_id_version = False found_gene_transcript = False for entry in FASTAReader_gen(fasta_arg): # Extract the transcript id by removing everything after the first space and then removing the version if needed transcript_id = remove_id_version(entry.header[1:].lstrip().split(' ')[0], force_remove_id_version) transcript = fetch_transcript_and_gene(conn, transcript_id) if not transcript and not found_gene_transcript: # We have not found a proper gene transcript in this file yet, # try to force the removal of the version from the transcript id transcript_id = remove_id_version(entry.header[1:].lstrip().split(' ')[0], True) transcript = fetch_transcript_and_gene(conn, transcript_id) # Remember that we need to force the removal for this file if transcript: force_remove_id_version = True force_remove_id_version_file_list.append(fasta_arg) print("Forcing removal of id version in FASTA file '%s'" % fasta_arg, file=sys.stderr) if not transcript: print(f"Transcript '{transcript_id}' in FASTA file '{fasta_arg}' not found in the gene feature information", file=sys.stderr) continue if options.filter != 'canonical': break found_gene_transcript = True if len(entry.sequence) % 3 != 0: continue transcript_biotype = transcript['biotype'] # This is the biotype of the transcript or, if that is NULL, the one of the gene if transcript_biotype and transcript_biotype != 'protein_coding': continue gene_transcripts_dict.setdefault(transcript['gene_id'], []).append((transcript_id, transcript['is_canonical'], len(entry.sequence))) if options.filter == 'canonical': selected_transcript_ids = [] for gene_id, transcript_tuples in gene_transcripts_dict.items(): canonical_transcript_ids = [id_ for (id_, is_canonical, _) in transcript_tuples if is_canonical] if not canonical_transcript_ids: # Select the transcript with the longest sequence. If more than # one transcripts have the same longest sequence for a gene, the # first one to appear in the FASTA file is selected. selected_transcript_id = max(transcript_tuples, key=lambda transcript_tuple: transcript_tuple[2])[0] elif len(canonical_transcript_ids) > 1: raise Exception("Gene %s has more than 1 canonical transcripts" % (gene_id)) else: selected_transcript_id = canonical_transcript_ids[0] selected_transcript_ids.append(selected_transcript_id) regions = [_.strip().lower() for _ in options.regions.split(",")] with open(options.of, 'w') as output_fasta_file, open(options.ff, 'w') as filtered_fasta_file: for fasta_arg in options.fasta: force_remove_id_version = fasta_arg in force_remove_id_version_file_list for entry in FASTAReader_gen(fasta_arg): transcript_id = remove_id_version(entry.header[1:].lstrip().split(' ')[0], force_remove_id_version) transcript = fetch_transcript_and_gene(conn, transcript_id) if not transcript: print(f"Transcript '{transcript_id}' in FASTA file '{fasta_arg}' not found in the gene feature information", file=sys.stderr) continue if options.filter == 'canonical': # We already filtered out non-protein-coding transcripts when populating gene_transcripts_dict if transcript_id not in selected_transcript_ids: continue elif options.filter == 'coding': if len(entry.sequence) % 3 != 0: print(f"Transcript '{transcript_id}' in FASTA file '{fasta_arg}' has a coding sequence length which is not multiple of 3, removing from FASTA output", file=sys.stderr) continue transcript_biotype = transcript['biotype'] # This is the biotype of the transcript or, if that is NULL, the one of the gene if transcript_biotype and transcript_biotype != 'protein_coding': print(f"Transcript {transcript_id} has biotype {transcript_biotype} (not protein-coding), removing from FASTA output", file=sys.stderr) continue if options.headers == "TranscriptId_species": # Change the FASTA header to '>TranscriptId_species', as required by TreeBest # Remove any underscore in the species entry.header = ">{}_{}".format(transcript_id, transcript['species'].replace('_', '')) elif options.headers == "TranscriptID-GeneSymbol_species": # Remove any underscore in the species entry.header = ">{}-{}_{}".format(transcript_id, transcript['gene_symbol'], transcript['species'].replace('_', '')) elif options.headers == "TranscriptID-TranscriptSymbol_species": # Remove any underscore in the species entry.header = ">{}-{}_{}".format(transcript_id, transcript['transcript_symbol'], transcript['species'].replace('_', '')) if transcript['seq_region_name'].lower() in regions: entry.print(filtered_fasta_file) else: entry.print(output_fasta_file) conn.close() if __name__ == '__main__': __main__()