Proactive Genomic Health Screening
Proactive Genomic Health Screening
A deeper look into your genome for smarter health decisions.
Your DNA carries valuable information that can help you better understand your health — not only today, but for the future. With Proactive Genomic Health Screening, you have the opportunity to uncover hidden genetic risks before symptoms arise, empowering you to make informed, preventive decisions about your well-being.
How It Works
Using a quick, non-invasive buccal swab (cheek swab), we collect a DNA sample that is analyzed using advanced next-generation sequencing (NGS) technology. This approach allows us to detect a wide range of inherited genetic changes, offering insights into multiple areas of health.
Depending on your needs for Proactive Genomic Health Screening, the analysis can be performed to provide different levels of detail and insight — from whole exome sequencing (WES), which covers all protein-coding regions, to whole genome sequencing (WGS), which analyzes your entire genetic code, or focused analysis of specific groups of genes (targeted panels), as indicated in the breakdown below.
Through a single sample, we can screen for potential risks in the following areas:
Hereditary Cancer Screening
Detect inherited mutations that increase the risk of cancers such as breast, ovarian, colorectal, prostate, and others — even before symptoms appear.
Empowering Your Health Journey
Whether you're seeking peace of mind, early awareness, or a deeper understanding of your genetic health, this screening gives you the tools to a proactive role in your health journey — with just one non-invasive test.