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samtools-fqidx(1) Bioinformatics tools samtools-fqidx(1) NAME samtools fqidx - indexes or queries regions from a fastq file SYNOPSIS samtools fqidx ref.fastq [region1 [...]] DESCRIPTION Index reference sequence in the FASTQ format or extract subsequence from indexed reference sequence. If no region is specified, fqidx will index the file and create <ref.fastq>.fai on the disk. If regions are specified, the subsequences will be retrieved and printed to stdout in the FASTQ format. The input and output can be files compressed in the BGZF format. When out- put is compressed, the default compression level is 4. The sequences in the input file should all have different names. If they do not, indexing will emit a warning about duplicate sequences and re- trieval will only produce subsequences from the first sequence with the du- plicated name. samtools fqidx should only be used on fastq files with a small number of entries. Trying to use it on a file containing millions of short sequenc- ing reads will produce an index that is almost as big as the original file, and searches using the index will be very slow and use a lot of memory. OPTIONS -o, --output FILE Write FASTQ to file rather than to stdout. If FILE ends with .gz, .bgz or .bgzf then it will be BGZF compressed. -n, --length INT Length for FASTQ sequence line wrapping. If zero, this means do not line wrap. Defaults to the line length in the input file. -c, --continue Continue working if a non-existent region is requested. -r, --region-file FILE Read regions from a file. Format is chr:from-to, one per line. -i, --reverse-complement Output the sequence as the reverse complement. When this option is used, "/rc" will be appended to the sequence names. To turn this off or change the string appended, use the --mark-strand option. --mark-strand TYPE Append strand indicator to sequence name. TYPE can be one of: rc Append '/rc' when writing the reverse complement. This is the default. no Do not append anything. sign Append '(+)' for forward strand or '(-)' for reverse comple- ment. This matches the output of "bedtools getfasta -s". custom,<pos>,<neg> Append string <pos> to names when writing the forward strand and <neg> when writing the reverse strand. Spaces are pre- served, so it is possible to move the indicator into the comment part of the description line by including a leading space in the strings <pos> and <neg>. --fai-idx FILE Read/Write to specified index file. --gzi-idx FILE Read/Write to specified compressed file index (used with .gz files). -h, --help Print help message and exit. --output-fmt-option OPT=VAL Set the output format options, level=0..9 for compression level 0 to 9. --write-index Create index for the output sequence data along with the output, in same path as <output name>.fai, <outputname>.gzi. This option is valid only for file output. -@, --threads N Set the number of extra threads for operations on compressed files. AUTHOR Written by Heng Li, with modifications by Andrew Whitwham and Robert Davies, all from the Sanger Institute. SEE ALSO samtools(1), samtools-faidx(1), samtools-fasta(1), samtools-fastq(1) Samtools website: <http://www.htslib.org/> samtools-1.23.1 18 March 2026 samtools-fqidx(1)
NAME | SYNOPSIS | DESCRIPTION | OPTIONS | AUTHOR | SEE ALSO
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