Reference

sqt(1)

SeQuencing Tools for biological DNA/RNA high-throughput data

NAME

sqt - SeQuencing Tools for biological DNA/RNA high-throughput data

DESCRIPTION

usage: sqt [-h] [--version]

{align, bam2fastq, fastxmod, qgramfreq, chars, fastagrep, readcov, randomseq, samsetop, bameof, readlenhisto, cutvect} ...

SeQuencing Tools -- command-line tools for working with sequencing data

positional arguments:

{align, bam2fastq, fastxmod, qgramfreq, chars, fastagrep, readcov, randomseq, samsetop, bameof, readlenhisto, cutvect}

align

Compare two strings

bam2fastq

Extract all reads from a BAM file that map to a certain location, but try hard

fastxmod

Modify FASTA and FASTQ files by picking subsets and modifying individual entries.

qgramfreq

Print q-gram (also called k-mer) frequencies in a FASTA or FASTQ file.

chars

Print the number of characters in a string.

fastagrep

Search for a IUPAC string in the sequences of a FASTA file.

readcov

Print a report for individual reads in a SAM/BAM file.

randomseq

Generate random sequences in FASTA format

samsetop

Perform set operation on two SAM/BAM files.

bameof

Check whether the EOF marker is present in BAM files.

readlenhisto

Print and optionally plot a read length histogram of one or more FASTA or FASTQ

cutvect

Remove vector sequence

optional arguments:

-h, --help

show this help message and exit

--version

show program's version number and exit

AUTHOR

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

History