A command-line utility for working with BINSEQ files.
bqtools provides tools to encode, decode, manipulate, and analyze BINSEQ files.
It supports both (*.bq) and (*.vbq) files and makes use of the binseq library.
BINSEQ is a binary file format family designed for high-performance processing of DNA sequences. It currently has two variants: BQ and VBQ.
- BQ (*.bq): Optimized for fixed-length DNA sequences without quality scores.
- VBQ (*.vbq): Optimized for variable-length DNA sequences with optional quality scores.
Both support single and paired sequences and make use of two-bit encoding for efficient nucleotide packing using bitnuc and efficient parallel FASTX processing using paraseq.
For more information about BINSEQ, see our preprint where we describe the format family and its applications.
- Encode: Convert FASTA or FASTQ files to a BINSEQ format
- Decode: Convert a BINSEQ file back to FASTA, FASTQ, or TSV format
- Cat: Concatenate multiple BINSEQ files
- Count: Count records in a BINSEQ file
- Grep: Search for fixed-string or regex patterns in BINSEQ files.
bqtools can be installed using cargo, the Rust package manager:
cargo install bqtoolsTo install cargo you can follow the instructions on the official Rust website.
# Clone the repository
git clone https://github.com/arcinstitute/bqtools.git
cd bqtools
# Install
cargo install --path .
# Check installation
bqtools --help# Get help information
bqtools --help
# Get help for specific commands
bqtools encode --help
bqtools decode --help
bqtools cat --help
bqtools count --helpbqtools accepts input from stdin or from file paths.
It will auto-determine the input format and compression status.
Convert FASTA/FASTQ files to BINSEQ:
# Encode a single file to bq
bqtools encode input.fastq -o output.bq
# Encode a single file to vbq
bqtools encode input.fastq -o output.vbq
# Encode a file stream to bq (auto-determine input format and compression status)
/bin/cat input.fastq.zst | bqtools encode -o output.bq
# Encode paired-end reads
bqtools encode input_R1.fastq input_R2.fastq -o output.bq
# Encode paired-end reads to vbq
bqtools encode input_R1.fastq input_R2.fastq -o output.vbq
# Encode a SAM/BAM/CRAM file to BINSEQ
bqtools encode input.bam -fb -o output.bq
# Encode an paired-end CRAM file to BINSEQ (sorted by read name)
bqtools encode input.paired.cram -I -fb -o output.vbq
# Specify a policy for handling non-ATCG nucleotides
bqtools encode input.fastq -o output.bq -p r # Randomly draw A/C/G/T for each N
# Set threads for parallel processing
bqtools encode input.fastq -o output.bq -T 4Available policies for handling non-ATCG nucleotides:
i: Ignore sequences with non-ATCG charactersp: Break on invalid sequencesr: Randomly draw a nucleotide for each N (default)a: Set all Ns to Ac: Set all Ns to Cg: Set all Ns to Gt: Set all Ns to T
You might have a directory or nested subdirectories with multiple FASTX files or FASTX file pairs.
bqtools makes use of the efficient walkdir crate to recursively identify all FASTX files with various compression formats.
It will then balance the provided file/file pairs among the thread pool to ensure efficient parallel encoding.
All options provided by bqtools encode will be passed through to the sub-encoders.
# Encode all FASTX files as BQ
bqtools encode --recursive --mode bq ./
# Encode all paired FASTX files as VBQ and index their output
bqtools encode --recursive --paired --mode vbq --index ./
# Encode recursively with a max-subdirectory depth of 2
bqtools encode --recursive --mode bq --depth 2 ./Convert BINSEQ files back to FASTA/FASTQ/TSV:
# Decode to FASTQ (default)
bqtools decode input.bq -o output.fastq
# Decode to compressed FASTQ (gzip/zstd)
bqtools decode input.bq -o output.fastq.gz
bqtools decode input.bq -o output.fastq.zst
# Decode to FASTA
bqtools decode input.bq -o output.fa -f a
# Decode paired-end reads into separate files
bqtools decode input.bq --prefix output
# Creates output_R1.fastq and output_R2.fastq
# Specify which read of a pair to output
bqtools decode input.bq -o output.fastq -m 1 # Only first read
bqtools decode input.bq -o output.fastq -m 2 # Only second read
# Specify output format
bqtools decode input.bq -o output.tsv -f t # TSV formatCombine multiple BINSEQ files:
bqtools cat file1.bq file2.bq file3.bq -o combined.bqCount records in a BINSEQ file:
bqtools count input.bqYou can easily search for specific subsequences or regular expressions within BINSEQ files:
# See full options list
bqtools grep --help
# Search for a specific subsequence (in primary sequence)
bqtools grep input.bq -e "ATCG"
# Search for a regular expression (in primary)
bqtools grep input.bq -r "AT[CG]"
# Search for both a subsequence (in extended sequence) and a regular expression (in either)
bqtools grep input.bq -E "ATCG" -P "AT[CG]"