SYNOPSIS

faidx [-h] [-b BED] [-o OUT] [-i {bed,chromsizes,nucleotide,transposed}] [-c] [-r] [-n | -f] [-x] [-l] [-s DEFAULT_SEQ] [-d DELIMITER] [-g REGEX] [-m | -M] [--version] fasta [regions [regions ...]]

DESCRIPTION

Fetch sequences from FASTA. If no regions are specified, all entries in the input file are returned. Input FASTA file must be consistently line-wrapped, and line wrapping of output is based on input line lengths.

OPTIONS

Positional arguments

fasta

FASTA file

regions

space separated regions of sequence to fetch e.g. chr1:1-1000

Optional arguments

-h, --help

show this help message and exit

-b BED, --bed BED

bed file of regions

-o OUT, --out OUT

output file name (default: stdout)

-i {bed,chromsizes,nucleotide,transposed}, --transform {bed,chromsizes,nucleotide,transposed}

transform the requested regions into another format. default: None

-c, --complement

complement the sequence. default: False

-r, --reverse

reverse the sequence. default: False

-n, --no-names

omit sequence names from output. default: False

-f, --full-names

output full names including description. default: False

-x, --split-files

write each region to a separate file (names are derived from regions)

-l, --lazy

fill in --default-seq for missing ranges. default: False

-s DEFAULT_SEQ, --default-seq DEFAULT_SEQ

default base for missing positions and masking. default: N

-d DELIMITER, --delimiter DELIMITER

delimiter for splitting names to multiple values (duplicate names will be discarded). default: None

-g REGEX, --regex REGEX

regular expression for filtering non-matching sequence names. default: .*

-m, --mask-with-default-seq

mask the FASTA file using --default-seq default: False

-M, --mask-by-case

mask the FASTA file by changing to lowercase. default: False

--version

print pyfaidx version number