Hi, I also have the quaddRAD seq data and reference genome. I used
ref_map.pl script in stacks to get the list of loci, so I'm able to concatenate nearby ones. I choose the distance in 10,000 bp between two loci to concatenate, is this an adequate choice? (My species diverged about 0.5 mya). Also, can I assume that if I accidentally concatenate two loci with different topologies, I won't have missed any information because the inconsistency will be reflected in the mbsum file for this big new locus?
Cheers
Ivan