We achieve 99% technical accuracy through high-depth sequencing and proprietary bioinformatics pipelines that filter out "noise." However, while the raw data is stable, the clinical significance of a gene can change as global research identifies new associations. We cross-reference your data with databases like ClinVar and PharmGKB to ensure interpretations meet current international standards.

Genetics is about predisposition. For example, having a variant in the TCF7L2 gene increases the risk of Type 2 Diabetes, but it doesn't guarantee diagnosis. By knowing your susceptibility, you can implement targeted preventive wellness strategies—such as specific dietary shifts or screenings—to effectively "silence" or mitigate those genetic risks.

We translate billions of data points into a color-coded report:

• Red (High Priority/Risk)
• Yellow (Moderate/Carrier)
• Green (Normal/Low Risk)

Each finding includes Actionable Insights—specific steps for nutrition (Nutrigenomics), fitness, and lifestyle. For deep dives, we provide post-report consultations to bridge the gap between complex lab data and daily application.

Your identity is decoupled from your DNA via a Unique Barcode System. Lab technicians see code, not names. Digital data is stored using AES-256 encryption. We adhere to strict ethical standards: we do not sell data to third parties, and we do not share results with insurance providers or employers without a signed, specific legal release from you.

We hold samples for 6 months to allow for "reflex testing" or quality verification if you have questions about your results. After this window, samples are incinerated as biohazardous waste. You may opt-in to Biobanking if you wish to participate in future longitudinal research studies, but this is entirely voluntary.

We use Buccal Swabs designed to collect a high concentration of epithelial cells. Unlike blood draws, this is non-invasive and stable at room temperature for shipping. It captures the same genomic DNA found in blood, ensuring no loss in sequencing quality.

The timeline accounts for DNA extraction, library preparation, NGS sequencing, and bioinformatics analysis. You can monitor the "Lab Pipeline" through your Personalized Dashboard, seeing exactly when your sample moves from "Received" to "Sequencing" to "Clinical Review."

Inconclusive results usually occur due to "low call rates" caused by insufficient DNA on the swab. If our QC (Quality Control) metrics aren't met, we won't issue a report based on "best guesses." Instead, we send a complimentary replacement kit to ensure the final data is 100% reliable.