run.sh

# !/bin/bash

# align sequences with default parameters (single linkage tree)
./famsa ./test/adeno_fiber/adeno_fiber sl.aln

# align sequences using UPGMA tree with 8 computing threads, store the result in the GZ archive
./famsa -gt upgma -t 8 -gz ./test/adeno_fiber/adeno_fiber upgma.aln.gz

# export a neighbour joining guide tree to the Newick format
./famsa -gt nj -gt_export ./test/adeno_fiber/adeno_fiber nj.dnd

# align sequences with the previously generated guide tree
./famsa -gt import nj.dnd ./test/adeno_fiber/adeno_fiber nj.aln

# align sequences with an approximated medoid guide tree and UPGMA subtrees
./famsa -medoidtree -gt upgma ./test/hemopexin/hemopexin upgma.medoid.aln

# export distance matrix to CSV format (lower triangular) 
./famsa -dist_export ./test/adeno_fiber/adeno_fiber dist.csv

# export pairwise identity (PID) matrix to CSV format (square) 
./famsa -dist_export -pid -square_matrix ./test/adeno_fiber/adeno_fiber pid.csv

# profile-profile alignment without refining output 
./famsa -refine_mode off ./test/adeno_fiber/upgma.no_refine.part1.fasta ./test/adeno_fiber/upgma.no_refine.part2.fasta pp.fasta