[REPLACE REPLACE website]
Panseq determines the core and accessory regions among a collection of genomic sequences based on user-defined parameters. It readily extracts regions unique to a genome or group of genomes, identifies SNPs within shared core genomic regions, constructs files for use in phylogeny programs based on both the presence/absence of accessory regions and SNPs within core regions.
module spider REPLACE to find out what environment modules are available for this application.
- HPC_REPLACE_DIR - installation directory
- HPC_REPLACE_BIN - executable directory