NAME

       qualityScores - toolkit for processing next-gen sequencing data

DESCRIPTION

       qualityScore Version 2.0.1

              Retrieve Phred score for read bases

       Usage:

              ./qualityScores [options] -i <input_file> -o <output_file>

       Required arguments:

       -i <string>
              Name of input file including read data. The default format is Fastq.

       -o <string>
              Name of output file that is a text file including Phred scores for each read base.

       Optional arguments:

       --gzFASTQinput Input file is in gzipped Fastq format.

       --BAMinput
              Input file is in BAM format.

       --SAMinput
              Input file is in SAM format.

       --first-end
              Use  only  first  reads  in paired-end data. Only applicable for paired-end BAM/SAM
              input.

       --second-end
              Use only second reads in paired-end data. Only applicable  for  paired-end  BAM/SAM
              input.

       --counted-reads <int> Total number of reads to be extracted from the input

              file. 10,000 by default.

       --phred-offset <33|64> refer to subread aligner.

AUTHOR

        This manpage was written by Nilesh Patra for the Debian distribution and
        can be used for any other usage of the program.