table of contents
SQT(1) | User Commands | SQT(1) |
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.
January 2019 | sqt 0.8.0 |