Find G-quadruplex motifs in sequencing reads/genome assemblies. Input is expected to be a fastq (optionally can be gzipped) or a fasta (if you're working with a genome assembly). Output is a bed file with the columns sequence_id, start, end, G4, length, strand. Default output is to stdout. See https://github.com/samtools/hts-specs/blob/master/BEDv1.pdf for more information on the BED file format.

The sequences are found via a regular expression explained in https://doi.org/10.1093/nar/gki609 with Rust Regex's find_iter() (https://docs.rs/regex/latest/regex/struct.Regex.html#method.find_iter) to avoid overlaps and repeating counts.

# The default output is to stdout, you can redirect it to a file. the output is in a standard bed file format. # quick run with cargo cargo run -- --reads /path/to/reads.fastq(.gz) > g4_motifs.bed # Works with multiple read files, and pipe the output to gzip/pigz before saving cargo run -- --reads ../*.fastq.gz | pigz > g4_motifs.bed.gz # Run on Polar2020 /data2/work/local/pg4Findr/pg4Findr --reads /path/to/read/or/assembly.fa | pigz > g4_motifs.bed.gz