NAME

       subread-fullscan - toolkit for processing next-gen sequencing data

DESCRIPTION

       subread-fullscan Version 2.0.1

              This program scans the entire genome to find all high-similarity locations to

       a specified read.

       Usage:

              ./subread-fullscan [options] -i <index_name> <read_string>

       Required arguments:

       -i <string>
              Base name of the index.

       read_string
              The read bases.

       Optional arguments:

       -m <float>
              The minimum fraction of matched bases in the read, 0.8 by default

AUTHOR

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