Mercurial > repos > blankenberg > naive_variant_caller
annotate tools/naive_variant_caller.py @ 1:ae6edc0012ba
Populate naive_variant_caller repository.
author | Daniel Blankenberg <dan@bx.psu.edu> |
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date | Thu, 29 Aug 2013 10:54:14 -0400 |
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children | 8398666758e3 |
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ae6edc0012ba
Populate naive_variant_caller repository.
Daniel Blankenberg <dan@bx.psu.edu>
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1 #Dan Blankenberg |
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2 import sys |
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3 import optparse |
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4 |
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5 from pyBamParser.bam import Reader |
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6 from pyBamTools.genotyping.naive import VCFReadGroupGenotyper |
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7 |
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8 def main(): |
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9 #Parse Command Line |
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10 parser = optparse.OptionParser() |
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11 parser.add_option( '-b', '--bam', dest='bam_file', action='append', type="string", default=[], help='BAM filename, optionally index filename. Multiple allowed.' ) |
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12 parser.add_option( '-i', '--index', dest='index_file', action='append', type="string", default=[], help='optionally index filename. Multiple allowed.' ) |
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13 parser.add_option( '-o', '--output_vcf_filename', dest='output_vcf_filename', action='store', default = None, type="string", help='Output VCF filename' ) |
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14 parser.add_option( '-r', '--reference_genome_filename', dest='reference_genome_filename', action='store', default = None, type="string", help='Input reference file' ) |
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15 parser.add_option( '-v', '--variants_only', dest='variants_only', action='store_true', default = False, help='Report only sites with a possible variant allele.' ) |
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16 parser.add_option( '-s', '--use_strand', dest='use_strand', action='store_true', default = False, help='Report counts by strand' ) |
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17 parser.add_option( '-p', '--ploidy', dest='ploidy', action='store', type="int", default=2, help='Ploidy. Default=2.' ) |
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18 parser.add_option( '-d', '--min_support_depth', dest='min_support_depth', action='store', type="int", default=0, help='Minimum number of reads needed to consider a REF/ALT. Default=0.' ) |
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19 parser.add_option( '-q', '--min_base_quality', dest='min_base_quality', action='store', type="int", default=None, help='Minimum base quality.' ) |
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20 parser.add_option( '-m', '--min_mapping_quality', dest='min_mapping_quality', action='store', type="int", default=None, help='Minimum mapping.' ) |
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21 parser.add_option( '-t', '--coverage_dtype', dest='coverage_dtype', action='store', type="string", default='uint8', help='dtype to use for coverage array' ) |
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22 parser.add_option( '--allow_out_of_bounds_positions', dest='allow_out_of_bounds_positions', action='store_true', default = False, help='Allows out of bounds positions to not throw fatal errors' ) |
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23 parser.add_option( '--region', dest='region', action='append', type="string", default=[], help='region' ) |
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24 (options, args) = parser.parse_args() |
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25 |
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26 if len( options.bam_file ) == 0: |
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27 print >>sys.stderr, 'You must provide at least one bam (-b) file.' |
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28 parser.print_help( sys.stderr ) |
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29 sys.exit( 1 ) |
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30 if options.index_file: |
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31 assert len( options.index_file ) == len( options.bam_file ), "If you provide a name for an index file, you must provide the index name for all bam files." |
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32 bam_files = zip( options.bam_file, options.index_file ) |
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33 else: |
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34 bam_files = [ ( x, ) for x in options.bam_file ] |
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35 if not options.reference_genome_filename: |
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36 print >> sys.stderr, "Warning: Reference file has not been specified. Providing a reference genome is highly recommended." |
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37 if options.output_vcf_filename: |
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38 out = open( options.output_vcf_filename, 'wb' ) |
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39 else: |
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40 out = sys.stdout |
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41 |
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42 regions = [] |
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43 if options.region: |
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44 for region in options.region: |
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45 region_split = region.split( ":" ) |
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46 region = region_split.pop( 0 ) |
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47 if region_split: |
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48 region_split = filter( bool, region_split[0].split( '-' ) ) |
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49 if region_split: |
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50 if len( region_split ) != 2: |
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51 print >> sys.stderr, "You must specify both a start and an end, or only a chromosome when specifying regions." |
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52 cleanup_before_exit( tmp_dir ) |
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53 sys.exit( 1 ) |
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54 region = tuple( [ region ] + map( int, region_split ) ) |
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55 regions.append( region ) |
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56 |
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57 coverage = VCFReadGroupGenotyper( map( lambda x: Reader( *x ), bam_files ), options.reference_genome_filename, dtype=options.coverage_dtype, |
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58 min_support_depth=options.min_support_depth, min_base_quality=options.min_base_quality, min_mapping_quality=options.min_mapping_quality, |
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59 restrict_regions=regions, use_strand=options.use_strand, allow_out_of_bounds_positions=options.allow_out_of_bounds_positions ) |
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60 for line in coverage.iter_vcf( ploidy=options.ploidy, variants_only=options.variants_only ): |
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61 out.write( "%s\n" % line ) |
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62 out.close() |
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63 |
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64 if __name__ == "__main__": main() |