In our database, we cover for all the significant and strongly associated genetic markers under each category type. We consider most of the markers tested in every population and we have especially added the ones that are studied for in Asian population. With Circle, we use whole-exome sequencing technlogy to read the protein-coding genes in the human genome to analyse 31 million data points (>100x more data than leading companies such as 23andme and Ancestry.com, whom both use genotyping technology).
When we sequence for the entire gene, unlike other personal genomic testing companies screening for specific variants in the gene, we look for every mutation present in the genes so that the likelihood of missing out on hundreds of other mutations with genotyping technology is reduced.