Mercurial > repos > dave > genebed_maf_to_fasta
view interval_maf_to_merged_fasta.py @ 0:be26293ade92 draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/genebed_maf_to_fasta/ commit 8d55cabcec17915d959f672ecacfa851df1f4ca4-dirty"
author | dave |
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date | Fri, 24 Jul 2020 12:35:57 -0400 |
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#!/usr/bin/env python """ Reads an interval or gene BED and a MAF Source. Produces a FASTA file containing the aligned intervals/gene sequences, based upon the provided coordinates Alignment blocks are layered ontop of each other based upon score. usage: %prog maf_file [options] -d, --dbkey=d: Database key, ie hg17 -c, --chromCol=c: Column of Chr -s, --startCol=s: Column of Start -e, --endCol=e: Column of End -S, --strandCol=S: Column of Strand -G, --geneBED: Input is a Gene BED file, process and join exons as one region -t, --mafSourceType=t: Type of MAF source to use -m, --mafSource=m: Path of source MAF file, if not using cached version -I, --mafIndex=I: Path of precomputed source MAF file index, if not using cached version -i, --interval_file=i: Input interval file -o, --output_file=o: Output MAF file -p, --species=p: Species to include in output -O, --overwrite_with_gaps=O: Overwrite bases found in a lower-scoring block with gaps interior to the sequence for a species. -z, --mafIndexFileDir=z: Directory of local maf_index.loc file usage: %prog dbkey_of_BED comma_separated_list_of_additional_dbkeys_to_extract comma_separated_list_of_indexed_maf_files input_gene_bed_file output_fasta_file cached|user GALAXY_DATA_INDEX_DIR """ # Dan Blankenberg from __future__ import print_function import sys import bx.intervals.io from bx.cookbook import doc_optparse from galaxy.tools.util import maf_utilities def stop_err(msg): sys.exit(msg) def __main__(): # Parse Command Line options, args = doc_optparse.parse(__doc__) mincols = 0 strand_col = -1 if options.dbkey: primary_species = options.dbkey else: primary_species = None if primary_species in [None, "?", "None"]: stop_err("You must specify a proper build in order to extract alignments. You can specify your genome build by clicking on the pencil icon associated with your interval file.") include_primary = True secondary_species = maf_utilities.parse_species_option(options.species) if secondary_species: species = list(secondary_species) # make copy of species list if primary_species in secondary_species: secondary_species.remove(primary_species) else: include_primary = False else: species = None if options.interval_file: interval_file = options.interval_file else: stop_err("Input interval file has not been specified.") if options.output_file: output_file = options.output_file else: stop_err("Output file has not been specified.") if not options.geneBED: if options.chromCol: chr_col = int(options.chromCol) - 1 else: stop_err("Chromosome column not set, click the pencil icon in the history item to set the metadata attributes.") if options.startCol: start_col = int(options.startCol) - 1 else: stop_err("Start column not set, click the pencil icon in the history item to set the metadata attributes.") if options.endCol: end_col = int(options.endCol) - 1 else: stop_err("End column not set, click the pencil icon in the history item to set the metadata attributes.") if options.strandCol: strand_col = int(options.strandCol) - 1 mafIndexFile = "%s/maf_index.loc" % options.mafIndexFileDir overwrite_with_gaps = True if options.overwrite_with_gaps and options.overwrite_with_gaps.lower() == 'false': overwrite_with_gaps = False # Finish parsing command line # get index for mafs based on type index = index_filename = None # using specified uid for locally cached if options.mafSourceType.lower() in ["cached"]: index = maf_utilities.maf_index_by_uid(options.mafSource, mafIndexFile) if index is None: stop_err("The MAF source specified (%s) appears to be invalid." % (options.mafSource)) elif options.mafSourceType.lower() in ["user"]: # index maf for use here, need to remove index_file when finished index, index_filename = maf_utilities.open_or_build_maf_index(options.mafSource, options.mafIndex, species=[primary_species]) if index is None: stop_err("Your MAF file appears to be malformed.") else: stop_err("Invalid MAF source type specified.") # open output file output = open(output_file, "w") if options.geneBED: region_enumerator = maf_utilities.line_enumerator(open(interval_file, "r").readlines()) else: region_enumerator = enumerate(bx.intervals.io.NiceReaderWrapper( open(interval_file, 'r'), chrom_col=chr_col, start_col=start_col, end_col=end_col, strand_col=strand_col, fix_strand=True, return_header=False, return_comments=False)) # Step through intervals regions_extracted = 0 line_count = 0 for line_count, line in region_enumerator: try: if options.geneBED: # Process as Gene BED try: starts, ends, fields = maf_utilities.get_starts_ends_fields_from_gene_bed(line) # create spliced alignment object alignment = maf_utilities.get_spliced_region_alignment( index, primary_species, fields[0], starts, ends, strand='+', species=species, mincols=mincols, overwrite_with_gaps=overwrite_with_gaps) primary_name = secondary_name = fields[3] alignment_strand = fields[5] except Exception as e: print("Error loading exon positions from input line %i: %s" % (line_count, e)) continue else: # Process as standard intervals try: # create spliced alignment object alignment = maf_utilities.get_region_alignment( index, primary_species, line.chrom, line.start, line.end, strand='+', species=species, mincols=mincols, overwrite_with_gaps=overwrite_with_gaps) primary_name = "%s(%s):%s-%s" % (line.chrom, line.strand, line.start, line.end) secondary_name = "" alignment_strand = line.strand except Exception as e: print("Error loading region positions from input line %i: %s" % (line_count, e)) continue # Write alignment to output file # Output primary species first, if requested if include_primary: output.write(">%s.%s\n" % (primary_species, primary_name)) if alignment_strand == "-": output.write(alignment.get_sequence_reverse_complement(primary_species)) else: output.write(alignment.get_sequence(primary_species)) output.write("\n") # Output all remainging species for spec in secondary_species or alignment.get_species_names(skip=primary_species): if secondary_name: output.write(">%s.%s\n" % (spec, secondary_name)) else: output.write(">%s\n" % (spec)) if alignment_strand == "-": output.write(alignment.get_sequence_reverse_complement(spec)) else: output.write(alignment.get_sequence(spec)) output.write("\n") output.write("\n") regions_extracted += 1 except Exception as e: print("Unexpected error from input line %i: %s" % (line_count, e)) raise # close output file output.close() # remove index file if created during run maf_utilities.remove_temp_index_file(index_filename) # Print message about success for user if regions_extracted > 0: print("%i regions were processed successfully." % (regions_extracted)) else: print("No regions were processed successfully.") if line_count > 0 and options.geneBED: print("This tool requires your input file to conform to the 12 column BED standard.") if __name__ == "__main__": __main__()