This method is unsuitable for high-density SNP genotyping because of the highly reduced representation. Although the cost and numbers of reads per sample are almost the same as existing methods (e.g. ~20 US dollars and ~1 M reads per sample for ddRADseq11), the number of SNPs is fewe...
Although the cost and numbers of reads per sample are almost the same as existing methods (e.g. ~20 US dollars and ~1 M reads per sample for ddRADseq11), the number of SNPs is fewer in our method (e.g. ~1,000 vs. ~100,000 SNPs), which means low efficiency in terms of ...