Mercurial > repos > xuebing > sharplabtool
diff tools/maf/interval_maf_to_merged_fasta.py @ 0:9071e359b9a3
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author | xuebing |
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date | Fri, 09 Mar 2012 19:37:19 -0500 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tools/maf/interval_maf_to_merged_fasta.py Fri Mar 09 19:37:19 2012 -0500 @@ -0,0 +1,196 @@ +#!/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 galaxy import eggs +from galaxy.tools.util import maf_utilities +import pkg_resources; pkg_resources.require( "bx-python" ) +from bx.cookbook import doc_optparse +import bx.intervals.io +import sys + +assert sys.version_info[:2] >= ( 2, 4 ) + +def stop_err( msg ): + sys.stderr.write( msg ) + sys.exit() + +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, 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, 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, e: + print "Unexpected error from input line %i: %s" % ( line_count, e ) + continue + + #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__()