The cost of sequencing a full human genome has dropped from nearly $100 million to just a few hundred dollars. This isn’t a minor price shift—it’s a complete reinvention of what’s possible in genomics. For decades, consumers expected little value from genetic tests because companies like 23andMe were limited to analyzing small portions of DNA. That limited analysis meant no insights into individual health, no guidance on family planning, no personalized medication dosages. At Nucleus Genomics, our view is very different. With AI, we're able to analyze entire genomes quickly and affordably, delivering real-world, medically relevant insight starting from a single swab.
Artificial intelligence isn’t just improving accuracy—it’s making population-scale personalized care viable. As a CLIA-certified and CAP-accredited medical provider, Nucleus isn’t a novelty or a toy. Our tests are physician-ordered, and the data is handled as securely as it would be in a hospital. Patients get full control over how, when, and where their data is used.
Too many people still fear sharing their genetic information. It’s time to set the record straight. Health insurers are legally barred from using your genetic information under the Genetic Information Nondiscrimination Act (GINA). That means safe access to a powerful tool that can help you understand disease risk, optimize treatment, and even ensure healthier children.
This is not the death of consumer genomics. It’s its transformation. And we’re leading it.