Whole Genome Sequencing (WGS) is the most comprehensive genetic test available, analyzing your entire DNA sequence—over 3 billion base pairs across all 23 pairs of chromosomes, along with mitochondrial DNA. Using 33× medical-grade coverage, WGS provides highly accurate and detailed genetic information, helping uncover inherited conditions, disease risks, and how your body may respond to treatments. It empowers individuals and clinicians with actionable insights for precision and personalized healthcare.
33x medical grade coverage
At-home blood sample collection
DNA is extracted and sequenced using advanced technology
Consent is needed
Licensed nurses & lab partners
Reach out to customer support for accessing sample report of the test
Results in 45 to 50 days
Whole Genome Sequencing (WGS) studies your entire DNA, giving the most complete view of your genetic makeup. It analyzes all genes and non-coding regions that influence how your body functions, helping identify inherited conditions, disease risks, cancer-related variants, and how your body may respond to medications. By looking at the full genome, WGS provides deeper, more comprehensive insights to support personalized and preventive healthcare decisions
Whole Genome Sequencing (WGS) may be recommended for individuals who have a family history of genetic disorders, experience unexplained or recurring health issues, show early-onset or multiple cancers, have developmental delays or congenital conditions, or display unusual responses to medications. It is also valuable for those seeking personalized, preventive, and long-term health insights.



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