subread-fullscan(1)
toolkit for processing next-gen sequencing data
Description
SUBREAD-FULLSCAN
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.