NAME
tqs - Trim Quality Solexa-Illumina Sequences
SYNOPSIS
Quality trim solexa-Illumina sequence reads using user-defined
thresholds.
OPTIONS
-h, --help
show this help message and exit
-f SEQFILE, --sequence file=SEQFILE
Illumina sequence file - Output format from the 1G Genome
Analyzer (_seq.txt):
7 1 255 669
AACCCCCACTCCTACAACGCCATCATTCCCCTCGAC
-q QUALFILE, --qual file=QUALFILE
A prb file containing all the Illumina intensities, as
outputted by the 1G Genome Analyzer (_prb.txt)
-l MER, --length=MER
Length of sequence reads (i.e. Number of sequencing cycles,
default=36)
-t THRESHOLD, --threshold=THRESHOLD
Base intensity threshold value (-40 to 40, default=5)
-d DIFF, --difference=DIFF
Base intensity difference between top intensity and second
best (1 to 80, default=5)
-c CONSEC, --consec=CONSEC
Minimum number of consecutive bases passing threshold values
(default=20)
-v, --verbose
Runs in Verbose mode.
SEE ALSO
/usr/share/doc/ssake/TQS.readme
AUTHORS
This manual page was written by Andreas Tille <tille@debian.org> for
the Debian system (but may be used by others). Permission is granted
to copy, distribute and/or modify this document under the terms of the
GNU General Public License, Version 2 any later version published by
the Free Software Foundation.
On Debian systems, the complete text of the GNU General Public License
can be found in /usr/share/common-licenses/GPL.
January 2008