tqs (1)

Quality trim solexa-Illumina sequence reads using user-defined thresholds.

-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.

/usr/share/doc/ssake/TQS.readme

This manual page was written by Andreas Tille <[email protected]> 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.