We only test for specific DNA segments or points of “glitches” that are associated with certain physiological, behavioural or hormonal traits. This approach gives our users more confidence and eliminates any uncertainty they might get from other DNA tests, that look at larger segments of DNA, with variants of uncertain significance.

We made a gene panel list through a genotyping technology that utilises competitive allele-specific microarrays. This enables highly accurate bi-allelic scoring of SNPs (99.8% accurate) and indels (insertions and deletions) at a specific loci, across a wide range of genomic DNA samples (SNP & indel assay conversion rate 90%). This means that the risk of false-positive and false-negative results are limited.

Once the results have been processed, the reports are then reviewed by our specialist partners, along with your provided health information. This is all obtained via our online platform in order to deliver an accurate assessment for each individual result.