Today’s advancements in clinical next-generation sequencing (NGS) have a profound impact on healthcare. NGS is not just giving clinicians a deeper understanding of disease, it is also unlocking previously unknown genetic anomalies that lead to better diagnoses and treatments of disease including:
- Cancer research
- Rare genetic diseases
- Infectious diseases (like COVID-19)
Additionally, the scalability and speed of these tests are making healthcare more affordable and helping patients live healthier lives.
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