Up to this point I've mostly used the default 3. How would one go about determining what the optimal abundance threshold is for a given dataset. I realize that kmer size selection has the greater effect on assembly quality and I've used kmergenie effectively for this on bacterial isolates in the past.
Any input is appreciated. Thanks.
Would that be the coverage cut-off metric? Thanks for the quick reply.
Yes, those terms are synonymous: abundance threshold (Minia), coverage cut-off (Kmergenie, Velvet)
Thanks for the clarification