17 October 2018 2 3K Report

I'm working with single nucleotide polymorphisms generated by genotyping by sequencing for a non-model organism. Since I do not have a reference genome, can two snp loci generated by gbs that overlap in sequence actually be representatives of different parts of the organism's genome? The probability of these 64 base pairs being exactly the same in two different parts of the genome are small I admit. But it's theoretically plausible, correct?

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