Mercurial > repos > iuc > data_manager_malt_index_builder
diff data_manager/malt_index_builder.py @ 0:5f9d6aee2256 draft default tip
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/data_managers/data_manager_malt_index_builder commit 710e56e0e522b0ed060dab2fecf05ed1c79c928f"
author | iuc |
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date | Wed, 17 Nov 2021 08:22:56 +0000 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/data_manager/malt_index_builder.py Wed Nov 17 08:22:56 2021 +0000 @@ -0,0 +1,98 @@ +#!/usr/bin/env python + +import json +import optparse +import os +import subprocess +import sys + + +def get_id_name(params, dbkey, fasta_description=None): + sequence_id = params['param_dict']['sequence_id'] + if not sequence_id: + sequence_id = dbkey + + sequence_name = params['param_dict']['sequence_name'] + if not sequence_name: + sequence_name = fasta_description + if not sequence_name: + sequence_name = dbkey + return sequence_id, sequence_name + + +def build_malt_index(data_manager_dict, fasta_filename, params, target_directory, dbkey, sequence_id, sequence_name, sequence_type, shapes, max_hits_per_seed, protein_reduct): + # The malt-build program produces a directory of files, + # so the data table path entry will be a directory and + # not an index file. + fasta_base_name = os.path.split(fasta_filename)[-1] + sym_linked_fasta_filename = os.path.join(target_directory, fasta_base_name) + os.symlink(fasta_filename, sym_linked_fasta_filename) + args = ['malt-build', '--input', sym_linked_fasta_filename, '--sequenceType', sequence_type, '--index', target_directory] + threads = os.environ.get('GALAXY_SLOTS') + if threads: + args.extend(['--threads', threads]) + if shapes is not None: + args.extend(['--shapes', shapes]) + if max_hits_per_seed is not None: + args.extend(['--maxHitsPerSeed', max_hits_per_seed]) + if protein_reduct is not None: + args.extend(['--proteinReduct', protein_reduct]) + proc = subprocess.Popen(args=args, shell=False, cwd=target_directory) + return_code = proc.wait() + if return_code: + sys.exit('Error building index, return_code: %d' % return_code) + # Remove unwanted files from the output directory. + os.remove(sym_linked_fasta_filename) + # The path entry here is the directory + # where the index files will be located, + # not a single index file (malt-build + # produces a directory if files, which + # is considered an index.. + data_table_entry = dict(value=sequence_id, dbkey=dbkey, name=sequence_name, path=None) + _add_data_table_entry(data_manager_dict, data_table_entry) + + +def _add_data_table_entry(data_manager_dict, data_table_entry): + data_table_name = "malt_indices" + data_manager_dict['data_tables'] = data_manager_dict.get('data_tables', {}) + data_manager_dict['data_tables'][data_table_name] = data_manager_dict['data_tables'].get(data_table_name, []) + data_manager_dict['data_tables'][data_table_name].append(data_table_entry) + return data_manager_dict + + +def main(): + parser = optparse.OptionParser() + parser.add_option('-f', '--fasta_filename', dest='fasta_filename', action='store', type="string", help='fasta filename') + parser.add_option('-d', '--fasta_dbkey', dest='fasta_dbkey', action='store', type="string", help='fasta dbkey') + parser.add_option('-t', '--fasta_description', dest='fasta_description', action='store', type="string", default=None, help='fasta description') + parser.add_option('-e', '--sequence_type', dest='sequence_type', action='store', type="string", help='DNA or Protein sequences') + parser.add_option('-p', '--shapes', dest='shapes', action='store', type="string", default=None, help='Comma-separated list of seed shapes') + parser.add_option('-m', '--max_hits_per_seed', dest='max_hits_per_seed', action='store', type="string", default=None, help='Maximum number of hits per seed') + parser.add_option('-r', '--protein_reduct', dest='protein_reduct', action='store', type="string", default=None, help='Name or definition of protein alphabet reduction') + (options, args) = parser.parse_args() + + filename = args[0] + + with open(filename) as fh: + params = json.load(fh) + target_directory = params['output_data'][0]['extra_files_path'] + os.mkdir(target_directory) + data_manager_dict = {} + + dbkey = options.fasta_dbkey + + if dbkey in [None, '', '?']: + raise Exception('"%s" is not a valid dbkey. You must specify a valid dbkey.' % (dbkey)) + + sequence_id, sequence_name = get_id_name(params, dbkey=dbkey, fasta_description=options.fasta_description) + + # Build the index. + build_malt_index(data_manager_dict, options.fasta_filename, params, target_directory, dbkey, sequence_id, sequence_name, options.sequence_type, options.shapes, options.max_hits_per_seed, options.protein_reduct) + + # Save info to json file. + with open(filename, 'w') as fh: + json.dump(data_manager_dict, fh, sort_keys=True) + + +if __name__ == "__main__": + main()