Whole Genome Testing – Individual Screening Report
Our Whole Genome Testing provides the most complete view of your DNA available today. Unlike targeted panels that examine only select genes, Whole Genome Sequencing reads your entire genetic code — all 20,000+ genes and the vast non-coding regions in between. This ensures that both common and rare variants are captured, including those not yet fully understood by science.
With this test, you receive:
Whole Genome Sequencing (WGS): Comprehensive analysis of your entire DNA sequence.
Variant Detection: Identification of known and novel genetic variants that may influence health, traits, or biological pathways.
Screening for Known Genetic Mutations: Detection of variants already documented in global databases that could impact health or wellness.
Individual Screening Report: A clear, easy-to-understand summary of key findings relevant to you — including insights into potential health risks, carrier status for inherited conditions, and overall genomic profile.
Secure Data Storage: Your raw sequencing data is stored safely for future reanalysis as science advances.
This test gives you a lifelong foundation of genetic information that can be revisited as new discoveries emerge, allowing ongoing updates and deeper interpretation over time.
Add-On: Couples Genetic Analysis
The Couples Analysis compares both partners’ genomes to identify shared carrier risks for inherited conditions that could affect future children. This powerful add-on helps couples understand their combined genetic compatibility and make proactive, informed decisions about family planning, fertility, and health.
With this add-on, you receive:
Cross-comparison of both genomes to identify shared recessive variants.
Assessment of potential reproductive risks and inherited conditions.
A joint report summarizing shared carrier findings and next-step recommendations.
Add-On: Family Genetic Analysis
The Family Analysis expands upon individual testing by connecting genomic data across parents, children, and extended relatives. This analysis helps identify hereditary patterns, shared variants, and potential risks that run within the family.
With this add-on, you receive:
Combined interpretation of multiple family members’ genomes.
Identification of inheritance patterns and shared genetic traits.
A comprehensive family genetics report outlining relationships between variants, risk factors, and shared health insights.
