Mercurial > repos > iuc > meme_fimo
view fimo_wrapper.py @ 4:cd54079f0f72 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/meme commit 9192c1e90e2fd5017e6044884bcc6f2e80ba8b31
author | iuc |
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date | Tue, 08 Mar 2016 08:10:52 -0500 |
parents | fd522a964017 |
children | eca84de658b0 |
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#!/usr/bin/env python import argparse import os import shutil import string import subprocess import sys import tempfile BUFFSIZE = 1048576 # Translation table for reverse Complement, with ambiguity codes. DNA_COMPLEMENT = string.maketrans("ACGTRYKMBDHVacgtrykmbdhv", "TGCAYRMKVHDBtgcayrmkvhdb") def reverse(sequence): # Reverse sequence string. return sequence[::-1] def dna_complement(sequence): # Complement DNA sequence string. return sequence.translate(DNA_COMPLEMENT) def dna_reverse_complement(sequence): # Returns the reverse complement of the sequence. sequence = reverse(sequence) return dna_complement(sequence) def stop_err(msg): sys.stderr.write(msg) sys.exit(1) parser = argparse.ArgumentParser() parser.add_argument('--input_motifs', dest='input_motifs', help='MEME output formatted files for input to fimo') parser.add_argument('--input_fasta', dest='input_fasta', help='Fassta sequence file') parser.add_argument('--options_type', dest='options_type', help='Basic or Advance options') parser.add_argument('--input_psp', dest='input_psp', default=None, help='File containing position specific priors') parser.add_argument('--input_prior_dist', dest='input_prior_dist', default=None, help='File containing binned distribution of priors') parser.add_argument('--alpha', dest='alpha', type=float, default=1.0, help='The alpha parameter for calculating position specific priors') parser.add_argument('--bgfile', dest='bgfile', default=None, help='Background file type, used only if not "default"') parser.add_argument('--max_strand', action='store_true', help='If matches on both strands at a given position satisfy the output threshold, only report the match for the strand with the higher score') parser.add_argument('--max_stored_scores', dest='max_stored_scores', type=int, help='Maximum score count to store') parser.add_argument('--motif', dest='motifs', action='append', default=[], help='Specify motif by id') parser.add_argument('--motif_pseudo', dest='motif_pseudo', type=float, default=0.1, help='Pseudocount to add to counts in motif matrix') parser.add_argument('--no_qvalue', action='store_true', help='Do not compute a q-value for each p-value') parser.add_argument('--norc', action='store_true', help='Do not score the reverse complement DNA strand') parser.add_argument('--output_path', dest='output_path', help='Output files directory') parser.add_argument('--parse_genomic_coord', action='store_true', help='Check each sequence header for UCSC style genomic coordinates') parser.add_argument('--qv_thresh', action='store_true', help='Use q-values for the output threshold') parser.add_argument('--thresh', dest='thresh', type=float, help='p-value threshold') parser.add_argument('--gff_output', dest='gff_output', help='Gff output file') parser.add_argument('--html_output', dest='html_output', help='HTML output file') parser.add_argument('--interval_output', dest='interval_output', help='Interval output file') parser.add_argument('--txt_output', dest='txt_output', help='Text output file') parser.add_argument('--xml_output', dest='xml_output', help='XML output file') args = parser.parse_args() fimo_cmd_list = ['fimo'] if args.options_type == 'advanced': fimo_cmd_list.append('--alpha %4f' % args.alpha) if args.bgfile is not None: fimo_cmd_list.append('--bgfile "%s"' % args.bgfile) if args.max_strand: fimo_cmd_list.append('--max-strand') fimo_cmd_list.append('--max-stored-scores %d' % args.max_stored_scores) if len(args.motifs) > 0: for motif in args.motifs: fimo_cmd_list.append('--motif "%s"' % motif) fimo_cmd_list.append('--motif-pseudo %4f' % args.motif_pseudo) if args.no_qvalue: fimo_cmd_list.append('--no-qvalue') if args.norc: fimo_cmd_list.append('--norc') if args.parse_genomic_coord: fimo_cmd_list.append('--parse-genomic-coord') if args.qv_thresh: fimo_cmd_list.append('--qv-thresh') fimo_cmd_list.append('--thresh %4f' % args.thresh) if args.input_psp is not None: fimo_cmd_list.append('--psp "%s"' % args.input_psp) if args.input_prior_dist is not None: fimo_cmd_list.append('--prior-dist "%s"' % args.input_prior_dist) fimo_cmd_list.append('--o "%s"' % (args.output_path)) fimo_cmd_list.append('--verbosity 1') fimo_cmd_list.append(args.input_motifs) fimo_cmd_list.append(args.input_fasta) fimo_cmd = ' '.join(fimo_cmd_list) try: tmp_stderr = tempfile.NamedTemporaryFile() proc = subprocess.Popen(args=fimo_cmd, shell=True, stderr=tmp_stderr) returncode = proc.wait() tmp_stderr.seek(0) stderr = '' try: while True: stderr += tmp_stderr.read(BUFFSIZE) if not stderr or len(stderr) % BUFFSIZE != 0: break except OverflowError: pass if returncode != 0: stop_err(stderr) except Exception, e: stop_err('Error running FIMO:\n%s' % str(e)) shutil.move(os.path.join(args.output_path, 'fimo.txt'), args.txt_output) shutil.move(os.path.join(args.output_path, 'fimo.gff'), args.gff_output) shutil.move(os.path.join(args.output_path, 'fimo.xml'), args.xml_output) shutil.move(os.path.join(args.output_path, 'fimo.html'), args.html_output) out_file = open(args.interval_output, 'wb') out_file.write("#%s\n" % "\t".join(("chr", "start", "end", "pattern name", "score", "strand", "matched sequence", "p-value", "q-value"))) for line in open(args.txt_output): if line.startswith('#'): continue fields = line.rstrip("\n\r").split("\t") start, end = int(fields[2]), int(fields[3]) sequence = fields[7] if start > end: # Flip start and end and set strand. start, end = end, start strand = "-" # We want sequences relative to strand; FIMO always provides + stranded sequence. sequence = dna_reverse_complement(sequence) else: strand = "+" # Make 0-based start position. start -= 1 out_file.write("%s\n" % "\t".join([fields[1], str(start), str(end), fields[0], fields[4], strand, sequence, fields[5], fields[6]])) out_file.close()