Does anyone have any advice/suggestions on how to deal with linked SNPs from short-read sequence data such as RADseq (i.e. multiple SNPs within a single locus) when assembling the observed SFS? If it's best to try to remove any linkage by, for example, retaining only the first SNP at each locus, then should the number of monomorphic sites be scaled down in any way - maybe by the proportion of SNPs that were retained/unlinked?