This document is for an in-development version of Galaxy. You can alternatively view this page in the latest release if it exists or view the top of the latest release's documentation.
Source code for galaxy.datatypes.converters.fastqsolexa_to_qual_converter
#!/usr/bin/env python """ convert fastqsolexa file to separated sequence and quality files. assume each sequence and quality score are contained in one line the order should be: 1st line: @title_of_seq 2nd line: nucleotides 3rd line: +title_of_qualityscore (might be skipped) 4th line: quality scores (in three forms: a. digits, b. ASCII codes, the first char as the coding base, c. ASCII codes without the first char.) Usage: %python fastqsolexa_to_qual_converter.py <your_fastqsolexa_filename> <output_seq_filename> <output_score_filename> """ import sys assert sys.version_info[:2] >= (2, 4)[docs]def stop_err(msg): sys.exit("%s" % msg)def __main__(): infile_name = sys.argv # datatype = sys.argv qual_title_startswith = '' seq_title_startswith = '' default_coding_value = 64 fastq_block_lines = 0 with open(infile_name) as fh, open(sys.argv, 'w') as outfile_score: for i, line in enumerate(fh): line = line.rstrip() if not line or line.startswith('#'): continue fastq_block_lines = (fastq_block_lines + 1) % 4 line_startswith = line[0:1] if fastq_block_lines == 1: # first line is @title_of_seq if not seq_title_startswith: seq_title_startswith = line_startswith if line_startswith != seq_title_startswith: stop_err('Invalid fastqsolexa format at line %d: %s.' % (i + 1, line)) read_title = line[1:] elif fastq_block_lines == 2: # second line is nucleotides read_length = len(line) elif fastq_block_lines == 3: # third line is +title_of_qualityscore (might be skipped) if not qual_title_startswith: qual_title_startswith = line_startswith if line_startswith != qual_title_startswith: stop_err('Invalid fastqsolexa format at line %d: %s.' % (i + 1, line)) quality_title = line[1:] if quality_title and read_title != quality_title: stop_err('Invalid fastqsolexa format at line %d: sequence title "%s" differes from score title "%s".' % (i + 1, read_title, quality_title)) if not quality_title: outfile_score.write('>%s\n' % read_title) else: outfile_score.write('>%s\n' % line[1:]) else: # fourth line is quality scores qual = '' fastq_integer = True # peek: ascii or digits? val = line.split() fastq_integer = True try: int(val) except ValueError: fastq_integer = False if fastq_integer: # digits qual = line else: # ascii quality_score_length = len(line) if quality_score_length == read_length + 1: quality_score_startswith = ord(line[0:1]) line = line[1:] elif quality_score_length == read_length: quality_score_startswith = default_coding_value else: stop_err('Invalid fastqsolexa format at line %d: the number of quality scores ( %d ) is not the same as bases ( %d ).' % (i + 1, quality_score_length, read_length)) for j, char in enumerate(line): score = ord(char) - quality_score_startswith # 64 qual = "%s%s " % (qual, str(score)) outfile_score.write('%s\n' % qual) if __name__ == "__main__": __main__()