sqt(1)
SeQuencing Tools for biological DNA/RNA high-throughput data
Description
SQT
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.