Mercurial > repos > nilshomer > srma_wrapper
diff srma_wrapper.py @ 0:9d60d2fce247 default tip
Migrated tool version 0.1.1 from old tool shed archive to new tool shed repository
author | nilshomer |
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date | Tue, 07 Jun 2011 17:43:07 -0400 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/srma_wrapper.py Tue Jun 07 17:43:07 2011 -0400 @@ -0,0 +1,116 @@ +#!/usr/bin/env python + +""" +Runs SRMA on a SAM/BAM file; +TODO: more documentation + +usage: srma_wrapper.py [options] + -r, --ref=r: The reference genome to use or index + -i, --input=i: The SAM/BAM input file + -o, --output=o: The SAM/BAM output file + -O, --offset=O: The alignment offset + -Q, --minMappingQuality=Q: The minimum mapping quality + -P, --minAlleleProbability=P: The minimum allele probability conditioned on coverage (for the binomial quantile). + -C, --minAlleleCoverage=C: The minimum haploid coverage for the consensus. Default value: 3. This option can be set + -R, --range=R: A range to examine + -c, --correctBases=c: Correct bases + -q, --useSequenceQualities=q: Use sequence qualities + -M, --maxHeapSize=M: The maximum number of nodes on the heap before re-alignment is ignored + -s, --fileSource=s: Whether to use a previously indexed reference sequence or one from history (indexed or history) + -p, --params=p: Parameter setting to use (pre_set or full) + -D, --dbkey=D: Dbkey for reference genome +""" + +import optparse, os, shutil, subprocess, sys, tempfile + +def stop_err( msg ): + sys.stderr.write( '%s\n' % msg ) + sys.exit() + +def __main__(): + #Parse Command Line + parser = optparse.OptionParser() + parser.add_option( '-r', '--ref', dest='ref', help='The reference genome to use or index' ) + parser.add_option( '-i', '--input', dest='input', help='The SAM/BAM input file' ) + parser.add_option( '-o', '--output', dest='output', help='The SAM/BAM output file' ) + parser.add_option( '-O', '--offset', dest='offset', help='The alignment offset' ) + parser.add_option( '-Q', '--minMappingQuality', dest='minMappingQuality', help='The minimum mapping quality' ) + parser.add_option( '-P', '--minAlleleProbability', dest='minAlleleProbability', help='The minimum allele probability conditioned on coverage (for the binomial quantile).' ) + parser.add_option( '-C', '--minAlleleCoverage', dest='minAlleleCoverage', help='The minimum haploid coverage for the consensus' ) + parser.add_option( '-R', '--range', dest='range', help='A range to examine' ) + parser.add_option( '-c', '--correctBases', dest='correctBases', help='Correct bases ' ) + parser.add_option( '-q', '--useSequenceQualities', dest='useSequenceQualities', help='Use sequence qualities ' ) + parser.add_option( '-M', '--maxHeapSize', dest='maxHeapSize', help='The maximum number of nodes on the heap before re-alignment is ignored' ) + parser.add_option( '-s', '--fileSource', dest='fileSource', help='Whether to use a previously indexed reference sequence or one from history (indexed or history)' ) + parser.add_option( '-p', '--params', dest='params', help='Parameter setting to use (pre_set or full)' ) + parser.add_option( '-D', '--dbkey', dest='dbkey', help='Dbkey for reference genome' ) + (options, args) = parser.parse_args() + + # make temp directory for bfast + tmp_dir = '%s/' % tempfile.mkdtemp() + + # assume indexing has already been done + if options.fileSource == 'history': + stop_err( 'Error: indexing not implemented' ) + + # set up aligning and generate aligning command options + if options.params == 'pre_set': + srma_cmds = '' + else: + if options.useSequenceQualities == 'true': + useSequenceQualities = 'true' + else: + useSequenceQualities = 'false' + ranges = 'null' + if options.range == 'None': + range = 'null' + else: + range = options.range + + srma_cmds = "OFFSET=%s MIN_MAPQ=%s MINIMUM_ALLELE_PROBABILITY=%s MINIMUM_ALLELE_COVERAGE=%s RANGES=%s RANGE=%s CORRECT_BASES=%s USE_SEQUENCE_QUALITIES=%s MAX_HEAP_SIZE=%s" % ( options.offset, options.minMappingQuality, options.minAlleleProbability, options.minAlleleCoverage, ranges, range, options.correctBases, options.useSequenceQualities, options.maxHeapSize ) + + # how do we call a JAR file? + cmd = 'java -jar /Users/nhomer/srma/build/jar/srma.jar I=%s O=%s R=%s %s' % ( options.input, options.output, options.ref, srma_cmds ) + + # perform alignments + buffsize = 1048576 + try: + # need to nest try-except in try-finally to handle 2.4 + try: + try: + tmp = tempfile.NamedTemporaryFile( dir=tmp_dir ).name + tmp_stderr = open( tmp, 'wb' ) + proc = subprocess.Popen( args=cmd, shell=True, cwd=tmp_dir, stderr=tmp_stderr.fileno() ) + returncode = proc.wait() + tmp_stderr.close() + # get stderr, allowing for case where it's very large + tmp_stderr = open( tmp, 'rb' ) + stderr = '' + try: + while True: + stderr += tmp_stderr.read( buffsize ) + if not stderr or len( stderr ) % buffsize != 0: + break + except OverflowError: + pass + tmp_stderr.close() + if returncode != 0: + raise Exception, stderr + except Exception, e: + raise Exception, 'Error executing SRMA. ' + str( e ) + # check that there are results in the output file + if os.path.getsize( options.output ) > 0: + if "0" == options.space: + sys.stdout.write( 'BFAST run on Base Space data' ) + else: + sys.stdout.write( 'BFAST run on Color Space data' ) + else: + raise Exception, 'The output file is empty. You may simply have no matches, or there may be an error with your input file or settings.' + except Exception, e: + stop_err( 'The alignment failed.\n' + str( e ) ) + finally: + # clean up temp dir + if os.path.exists( tmp_dir ): + shutil.rmtree( tmp_dir ) + +if __name__=="__main__": __main__()