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

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

subread-fullscan 2.0.3                             March 2023                                SUBREAD-FULLSCAN(1)

       subread-fullscan Version 2.0.4

              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

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