table of contents
PULLSEQ(1) | User Commands | PULLSEQ(1) |
NAME¶
pullseq - <short_description>
DESCRIPTION¶
pullseq - a bioinformatics tool for manipulating fasta and fastq files
Version: 1.0.2 Name lookup method: UTHASH (Written by bct - copyright 2012-2015)
Usage:¶
- pullseq -i <input fasta/fastq file> -n <header names to select>
- pullseq -i <input fasta/fastq file> -m <minimum sequence length>
- pullseq -i <input fasta/fastq file> -g <regex name to match>
- pullseq -i <input fasta/fastq file> -m <minimum sequence length> -a <max sequence length>
- pullseq -i <input fasta/fastq file> -t
- cat <names to select from STDIN> | pullseq -i <input fasta/fastq file> -N
- Options:
- -i, --input,
- Input fasta/fastq file (required)
- -n, --names,
- File of header id names to search for
-N, --names_stdin, Use STDIN for header id names
- -g, --regex,
- Regular expression to match (PERL compatible; always case-insensitive)
- -m, --min,
- Minimum sequence length
- -a, --max,
- Maximum sequence length
- -l, --length,
- Sequence characters per line (default 50)
- -c, --convert,
- Convert input to fastq/fasta (e.g. if input is fastq, output will be fasta)
- -q, --quality,
- ASCII code to use for fasta->fastq quality conversions
- -e, --excluded,
- Exclude the header id names in the list (-n)
- -t, --count,
- Just count the possible output, but don't write it
- -h, --help,
- Display this help and exit
- -v, --verbose,
- Print extra details during the run
- --version,
- Output version information and exit
AUTHOR¶
This manpage was written by Nilesh Patra for the Debian
distribution and
can be used for any other usage of the program.
March 2021 | pullseq 1.0.2 |