| Description |
The product contains information-rich genome-wide tagged SNPs, other high-value markers (including insertion deletions and updated exome-based content), and can incorporate up to 300,000 semi-customized markers. In addition to enabling cost-effective large-scale genotyping studies, it provides easy and rapid access to baseline sample datasets for a variety of downstream applications, such as for common variant, mtDNA, ancestry, sex identification, deletion variant, insertion deletion, and CNV detection studies. |
