Provided by: fastani_1.33-3_amd64 

NAME
fastANI - Fast alignment-free computation of whole-genome Average Nucleotide Identity
DESCRIPTION
----------------- fastANI is a fast alignment-free implementation for computing whole-genome Average Nucleotide Identity (ANI) between genomes ----------------- Example usage: $ fastANI -q genome1.fa -r genome2.fa -o output.txt $ fastANI -q genome1.fa --rl genome_list.txt -o output.txt Available options ----------------- -h, --help Print this help page -r <value>, --ref <value> reference genome (fasta/fastq)[.gz] --refList <value>, --rl <value> a file containing list of reference genome files, one genome per line -q <value>, --query <value> query genome (fasta/fastq)[.gz] --ql <value>, --queryList <value> a file containing list of query genome files, one genome per line -k <value>, --kmer <value> kmer size <= 16 [default : 16] -t <value>, --threads <value> thread count for parallel execution [default : 1] --fragLen <value> fragment length [default : 3,000] --minFraction <value> minimum fraction of genome that must be shared for trusting ANI. If reference and query genome size differ, smaller one among the two is considered. [default : 0.2] --visualize output mappings for visualization, can be enabled for single genome to single genome comparison only [disabled by default] --matrix also output ANI values as lower triangular matrix (format inspired from phylip). If enabled, you should expect an output file with .matrix extension [disabled by default] -o <value>, --output <value> [required] output file name -v, --version Show version
AUTHOR
This manpage was written by Nilesh Patra for the Debian distribution and can be used for any other usage of the program. fastANI 1.32 March 2021 FASTANI(1)