Mercurial > repos > devteam > fastq_filter
view fastq_filter.py @ 1:b957f55f3955 draft
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tool_collections/galaxy_sequence_utils/fastq_filter commit a1517c9d22029095120643bbe2c8fa53754dd2b7
author | devteam |
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date | Wed, 11 Nov 2015 12:40:42 -0500 |
parents | 30d9ece6c752 |
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#Dan Blankenberg import sys, os, shutil from galaxy_utils.sequence.fastq import fastqReader, fastqWriter def main(): #Read command line arguments input_filename = sys.argv[1] script_filename = sys.argv[2] output_filename = sys.argv[3] additional_files_path = sys.argv[4] input_type = sys.argv[5] or 'sanger' #Save script file for debuging/verification info later os.mkdir( additional_files_path ) shutil.copy( script_filename, os.path.join( additional_files_path, 'debug.txt' ) ) ## Dan, Others: Can we simply drop the "format=input_type" here since it is specified in reader. ## This optimization would cut runtime roughly in half (for my test case anyway). -John out = fastqWriter( open( output_filename, 'wb' ), format = input_type ) i = None reads_kept = 0 execfile(script_filename, globals()) for i, fastq_read in enumerate( fastqReader( open( input_filename ), format = input_type ) ): ret_val = fastq_read_pass_filter( fastq_read ) ## fastq_read_pass_filter defined in script_filename if ret_val: out.write( fastq_read ) reads_kept += 1 out.close() if i is None: print "Your file contains no valid fastq reads." else: print 'Kept %s of %s reads (%.2f%%).' % ( reads_kept, i + 1, float( reads_kept ) / float( i + 1 ) * 100.0 ) if __name__ == "__main__": main()