We only test for specific DNA segments or points of “glitches” that have been strongly associated with certain physiological, behavioural or hormonal traits. We use this approach to bring more certainty to our users and eliminate ambiguities brought by other DNA testing offerings that look at larger segments of DNA with variants of uncertain significance (VUS).
Our gene panel list is assayed through a genotyping technology that utilises competitive allele-specific PCR, which enables highly accurate bi-allelic scoring of SNPs (99.8% accurate) and indels (insertions and deletions) at specific loci across a wide range of genomic DNA samples (SNP & indel assay conversion rate 90%), thereby limiting the risk of false-positive and false-negative results.
Once the results have been processed, the reports are then reviewed by our specialist partners, along with your provided health information, via our online platform in order to deliver an accurate assessment for each individual result.
All users sensitive data and genetic info is stored in our database in anonymised and encrypted format.
We use a multi-level security system on all application layers.
Apps development was built using CQRS and DDD patterns.
All data transfers are secured over standard SSL SHA-256 ECDSA.
Data held in a secure database server and protected by a dedicated firewall.