sak man page

sak — Slicing and dicing of FASTA/FASTQ files..

Synopsis

sak [Options] [-o OUT.{fa,fq}] IN.{fa,fq}

Description

"It slices, it dices and it makes the laundry!"

Original SAK tool by David Weese. Rewrite by Manuel Holtgrewe.

Required Arguments

IN INPUT_FILE

Valid filetypes are: .sam, .raw, .gbk, .frn, .fq, .fna, .ffn, .fastq, .fasta, .faa, .fa, and .embl.

Options

-h, --help

Display the help message.

--version

Display version information.

Output Options

-o, --out-path OUTPUT_FILE

Path to the resulting file.  If omitted, result is printed to stdout in FastQ format. Valid filetypes are: .sam, .raw, .frn, .fq, .fna, .ffn, .fastq, .fasta, .faa, and .fa.

-rc, --revcomp

Reverse-complement output.

-l, --max-length INTEGER

Maximal number of sequence characters to write out.

Filter Options

-s, --sequence List of INTEGER's

Select the given sequence for extraction by 0-based index.

-sn, --sequence-name List of STRING's

Select sequence with name prefix being NAME.

-ss, --sequences List of STRING's

Select sequences from-to where from and to are 0-based indices.

-i, --infix List of STRING's

Select characters from-to where from and to are 0-based indices.

-ll, --line-length INTEGER

Set line length in output file.  See section Line Length for details. In range [-1..inf].

Line Length

You can use the setting --line-length for setting the resulting line length.  By default, sequences in FASTA files are written with at most 70 characters per line and sequences in FASTQ files are written without any line breaks.  The quality sequence in FASTQ file is written in the same way as the residue sequence.

The default is selected with a --line-length value of -1 and line breaks can be disabled with a value of 0.

Usage Examples

sak -s 10 IN.fa

Cut out 11th sequence from IN.fa and write to stdout as FASTA.

sak -ss 10-12 -ss 100-200 IN.fq

Cut out 11th up to and including 12th and 101th up to and including 199th sequence from IN.fq and write to stdout as FASTA.

Info

sak 0.4.8 [tarball]