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
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()