Provided by: fastani_1.33-2build1_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.