----------------- 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