Mercurial > repos > galaxyp > retrieve_ensembl_bed
diff retrieve_ensembl_bed.py @ 0:da1b538b87e5 draft
planemo upload for repository https://github.com/galaxyproteomics/tools-galaxyp/tree/master/tools/proteogenomics/retrieve_ensembl_bed commit 88cf1e923a8c9e5bc6953ad412d15a7c70f054d1
author | galaxyp |
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date | Mon, 22 Jan 2018 13:13:47 -0500 |
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children | 9c4a48f5d4e7 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/retrieve_ensembl_bed.py Mon Jan 22 13:13:47 2018 -0500 @@ -0,0 +1,155 @@ +#!/usr/bin/env python +""" +# +#------------------------------------------------------------------------------ +# University of Minnesota +# Copyright 2017, Regents of the University of Minnesota +#------------------------------------------------------------------------------ +# Author: +# +# James E Johnson +# +#------------------------------------------------------------------------------ +""" + +from __future__ import print_function + +import argparse +import re +import sys + +from bedutil import bed_from_line + +from ensembl_rest import get_toplevel, get_transcripts_bed, max_region + + +def __main__(): + parser = argparse.ArgumentParser( + description='Retrieve Ensembl cDNAs in BED format') + parser.add_argument( + '-s', '--species', default='human', + help='Ensembl Species to retrieve') + parser.add_argument( + '-R', '--regions', action='append', default=[], + help='Restrict Ensembl retrieval to regions e.g.:' + + ' X,2:20000-25000,3:100-500+') + parser.add_argument( + '-B', '--biotypes', action='append', default=[], + help='Restrict Ensembl biotypes to retrieve') + parser.add_argument( + '-X', '--extended_bed', action='store_true', default=False, + help='Include the extended columns returned from Ensembl') + parser.add_argument( + '-U', '--ucsc_chrom_names', action='store_true', default=False, + help='Use the UCSC names for Chromosomes') + parser.add_argument( + '-t', '--toplevel', action='store_true', + help='Print Ensembl toplevel for species') + parser.add_argument( + 'output', + help='Output BED filepath, or for stdout: "-"') + parser.add_argument('-v', '--verbose', action='store_true', help='Verbose') + parser.add_argument('-d', '--debug', action='store_true', help='Debug') + args = parser.parse_args() + species = args.species + out_wtr = open(args.output, 'w') if args.output != '-' else sys.stdout + biotypes = ';'.join(['biotype=%s' % bt.strip() + for biotype in args.biotypes + for bt in biotype.split(',') if bt.strip()]) + + selected_regions = dict() # chrom:(start, end) + region_pat = '^([^:]+)(?::(\d*)(?:-(\d+)([+-])?)?)?' + if args.regions: + for entry in args.regions: + if not entry: + continue + regs = [x.strip() for x in entry.split(',') if x.strip()] + for reg in regs: + m = re.match(region_pat, reg) + if m: + (chrom, start, end, strand) = m.groups() + if chrom: + if chrom not in selected_regions: + selected_regions[chrom] = [] + selected_regions[chrom].append([start, end, strand]) + if args.debug: + print("selected_regions: %s" % selected_regions, file=sys.stderr) + + def retrieve_region(species, ref, start, stop, strand): + transcript_count = 0 + regions = list(range(start, stop, max_region)) + if not regions or regions[-1] < stop: + regions.append(stop) + for end in regions[1:]: + bedlines = get_transcripts_bed(species, ref, start, end, + strand=strand, params=biotypes) + if args.debug: + print("%s\t%s\tstart: %d\tend: %d\tcDNA transcripts:%d" % + (species, ref, start, end, len(bedlines)), + file=sys.stderr) + # start, end, seq + for i, bedline in enumerate(bedlines): + if args.debug: + print("%s\n" % (bedline), file=sys.stderr) + if not args.ucsc_chrom_names: + bedline = re.sub('^[^\t]+', ref, bedline) + try: + if out_wtr: + out_wtr.write(bedline.replace(',\t', '\t') + if args.extended_bed + else str(bed_from_line(bedline))) + out_wtr.write("\n") + out_wtr.flush() + except Exception as e: + print("BED error (%s) : %s\n" % (e, bedline), + file=sys.stderr) + start = end + 1 + return transcript_count + + coord_systems = get_toplevel(species) + if 'chromosome' in coord_systems: + ref_lengths = dict() + for ref in sorted(coord_systems['chromosome'].keys()): + length = coord_systems['chromosome'][ref] + ref_lengths[ref] = length + if args.toplevel: + print("%s\t%s\tlength: %d" % (species, ref, length), + file=sys.stderr) + if selected_regions: + transcript_count = 0 + for ref in sorted(selected_regions.keys()): + if ref in ref_lengths: + for reg in selected_regions[ref]: + (_start, _stop, _strand) = reg + start = int(_start) if _start else 0 + stop = int(_stop) if _stop else ref_lengths[ref] + strand = '' if not _strand else ':1'\ + if _strand == '+' else ':-1' + transcript_count += retrieve_region(species, ref, + start, stop, + strand) + if args.debug or args.verbose: + length = stop - start + print("%s\t%s:%d-%d%s\tlength: %d\ttrancripts:%d" % + (species, ref, start, stop, strand, + length, transcript_count), + file=sys.stderr) + else: + strand = '' + start = 0 + for ref in sorted(ref_lengths.keys()): + length = ref_lengths[ref] + transcript_count = 0 + if args.debug: + print("Retrieving transcripts: %s\t%s\tlength: %d" % + (species, ref, length), file=sys.stderr) + transcript_count += retrieve_region(species, ref, start, + length, strand) + if args.debug or args.verbose: + print("%s\t%s\tlength: %d\ttrancripts:%d" % + (species, ref, length, transcript_count), + file=sys.stderr) + + +if __name__ == "__main__": + __main__()