Your genetic blueprint, at the heart of your care.

Your DNA isn’t just data — it’s a personal health map. Within it are clues that can explain why you respond to certain treatments, why you may be at risk for certain conditions, and how to prevent them before they start.

HAVE A BETTER LIFE WITH MENDLY

Our DNA-first approach can cut through years of uncertainty by placing your genomic data at the starting line of your care.

Whole genome sequencing

We sequence your entire DNA, capturing every region of your genome with the precision needed to detect not only known genetic conditions, but also rare or entirely unique variants present only in your DNA. In contrast, the usual approach — genotyping — that can only identify variants already catalogued in research databases, leaving novel mutations undetected.

Symptom-driven testing

Whenever you report a symptom, our system instantly checks your DNA for the most relevant genetic tests. No wasted time, no unnecessary worry—just the insights you need exactly when you need them. This keeps your care fast, focused, and stress-free, letting you and your doctor act with confidence.

Safer treatment

DNA first enables pharmacogenetics: your treatment is personalized from day one—minimizing risks and maximizing effectiveness. By understanding your unique genetic blueprint upfront, Mendly helps your healthcare team choose the safest medications and dosages tailored just for you. We protect you from harmful side effects and speed up your recovery!

Faster diagnosis

Your DNA is analyzed from the very start, leaving zero chance for a 6 years diagnosis odyssey. Even non-genetic conditions are diagnosed faster, as our system prioritizes likely causes when DNA insights rule out genetic risk. The result: rapid, precise guidance with no room for harmful trial-and-error treatments.