grepq 1.2.0

quickly filter FASTQ files by matching sequences to a set of regex patterns

Feature set

(italics signifies a new feature added to the latest version)

• very fast and scales to large FASTQ files
• gzip support
• JSON support for pattern file input and tune subcommand output, allowing named regex sets and named regex patterns. Validation of the JSON pattern file is performed before processing (see the schema.json file in the examples directory)
• does not match false positives
• output matched sequences to one of three formats
• tune your pattern file with the tune subcommand
• supports inverted matching with the inverted subcommand
• plays nicely with your unix workflows

Features and performance in detail

1. Very fast and scales to large FASTQ files

2022 model Mac Studio with 32GB RAM and Apple M1 max chip running macOS 15.0.1. The FASTQ file (SRX26365298.fastq) was 874MB in size and was stored on the internal SSD (APPLE SSD AP0512R). The pattern file contained 30 regex patterns (see examples/regex.txt for the patterns used). Under the same conditions and using the same pattern file, grepq processed a 104GB FASTQ file in 26 seconds (4GB/s) (grepq v1.1.8, ripgrep v14.1.1 and grep 2.6.0-FreeBSD. ripgrep and grep were run with the default settings).

2. Reads and writes regular or gzip-compressed FASTQ files

Use the --best option for best compression, or the --fast option for faster compression.

Conditions and versions as above, but the FASTQ file was gzip-compressed. grepq was run with the -x option, ripgrep with the -z option, and grep with the -Z option.

3. Does not match false positives

grepq will only match regex patterns to the sequence field of a FASTQ record, which is the most common use case. Unlike ripgrep and grep, which will match the regex patterns to the entire FASTQ record, which includes the record ID, sequence, separator, and quality. This can lead to false positives and slow down the filtering process.

4. Output matched sequences to one of three formats

• sequences only (default)
• sequences and their corresponding record IDs (-I option)
• FASTQ format (-R option)

5. Will tune your pattern file with the tune subcommand

Use the tune subcommand to analyze matched substrings and update the number and/or order of regex patterns in your pattern file according to their matched frequency. This can speed up the filtering process.

Specifying the -c option to the tune subcommand will output the matched substrings and their frequencies, ranked from highest to lowest.

When the patterns file is given in JSON format (specified with the -j option), then specifying the -c, --names and --json-matches options to the tune subcommand will output the matched substrings and their frequencies in JSON format to a file called matches.json, allowing named regex sets and named regex patterns. See examples/regex.json for an example of a JSON pattern file and examples/matches.json for an example of the output of the tune subcommand in JSON format.

[!NOTE] When the count option (-c) is given with the tune subcommand, grepq will count the number of FASTQ records containing a sequence that is matched, for each matching regex in the pattern file. If, however, there are multiple occurrences of a given regex within a FASTQ record sequence field, grepq will count this as one match.

When the count option (-c) is not given with the tune subcommand, grepq provides the total number of matching FASTQ records for the set of regex patterns in the pattern file.

6. Supports inverted matching with the inverted subcommand

Use the inverted subcommand to output sequences that do not match any of the regex patterns in your pattern file.

7. Plays nicely with your unix workflows

For example, see tune.sh in the examples directory. This simple script will filter a FASTQ file using grepq, tune the pattern file on a user-specified number of FASTQ records, and then filter the FASTQ file again using the tuned pattern file for a user-specified number of the most frequent regex pattern matches.

Usage

Get instructions and examples using grepq -h, and grepq tune -h and grepq inverted -h for more information on the tune and inverted subcommands, respectively.

Pattern files must contain one regex pattern per line, and patterns are case-sensitive (you can supply an empty pattern file to count the total number of records in the FASTQ file). The regex patterns should only include the DNA sequence characters (A, C, G, T), and not other IUPAC codes (e.g., not N, R, Y, etc.). If your regex patterns contain any of these other IUPAC codes, then transform them to DNA sequence characters (A, C, G, T) before using them with grepq. See regex.txt and regex.json in the examples directory for examples of valid pattern files.

Requirements

• grepq has been tested on Linux and macOS. It might work on Windows, but it has not been tested.
• Ensure that Rust is installed on your system (https://www.rust-lang.org/tools/install)
• If the build fails, make sure you have the latest version of the Rust compiler by running rustup update

Installation

• From crates.io (easiest method)

  • cargo install grepq

• From source

  • Clone the repository and cd into the grepq directory
  • Run cargo build --release
  • Relative to the cloned parent directory, the executable will be located in ./target/release
  • Make sure the executable is in your PATH or use the full path to the executable

Examples

Get instructions and examples using grepq -h, and grepq tune -h and grepq inverted -h for more information on the tune and inverted subcommands, respectively. See the examples directory for examples of pattern files and FASTQ files.

File sizes of outfiles to verify grepq is working correctly, using the regex file regex.txt and the small fastq file small.fastq, both located in the examples directory:

grepq ./examples/regex.txt ./examples/small.fastq > outfile.txt 
15953

grepq  ./examples/regex.txt ./examples/small.fastq inverted > outfile.txt
736547

grepq -I ./examples/regex.txt ./examples/small.fastq > outfile.txt
19515

grepq -I ./examples/regex.txt ./examples/small.fastq inverted > outfile.txt 
901271

grepq -R ./examples/regex.txt ./examples/small.fastq > outfile.txt
35574

grepq -R ./examples/regex.txt ./examples/small.fastq inverted > outfile.txt 
1642712

• SARS-CoV-2 example

Count of the top five most frequently matched patterns found in SRX26602697.fastq using the pattern file SARS-CoV-2.txt (this pattern file contains 64 sequences of length 60 from Table II of this preprint):

time grepq SARS-CoV-2.txt SRX26602697.fastq tune -n 10000 -c | head -5
GTATGGAAAAGTTATGTGCATGTTGTAGACGGTTGTAATTCATCAACTTGTATGATGTGT: 1595
CGGAACGTTCTGAAAAGAGCTATGAATTGCAGACACCTTTTGAAATTAAATTGGCAAAGA: 693
TCCTTACTGCGCTTCGATTGTGTGCGTACTGCTGCAATATTGTTAACGTGAGTCTTGTAA: 356
GCGCTTCGATTGTGTGCGTACTGCTGCAATATTGTTAACGTGAGTCTTGTAAAACCTTCT: 332
CCGTAGCTGGTGTCTCTATCTGTAGTACTATGACCAATAGACAGTTTCATCAAAAATTAT: 209

________________________________________________________
Executed in  236.47 millis    fish           external
   usr time  203.88 millis    0.12 millis  203.76 millis
   sys time   34.74 millis   13.57 millis   21.16 millis

Update changes

see CHANGELOG

License

MIT