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100X Whole Exome Sequencing

TARGETED PRECISION. LIFELONG BENEFITS

Decode the most important 1–2% of your genome, THE EXOME, with 100× Whole Exome Sequencing. This ultra-deep test focuses on the regions that matter most: your protein-coding genes, where over 85% of disease-causing mutations are found.

Includes 20% OFF expert genetic counseling to help you interpret and act on your results.

CLINICALLY MEANINGFUL. HIGH-CONFIDENCE RESULTS.

100X coverage ensures that each protein-coding region is sequenced approximately 100 times for elite accuracy enabling better diagnostic confidence, especially for rare or complex conditions.

NOT JUST DATA, BUT DECISIONS BACKED BY YOUR OWN GENETICS.

Price 499.00 USD
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Focused Clinical Accuracy: Targets exons, the parts of your genome most relevant to
health and disease. Ideal for diagnosing inherited and rare genetic conditions.

Ultra-Deep Coverage (100X): High read depth ensures maximum confidence in variant
detection, reducing false positives and uncovering even subtle mutations.

Turnaround Time Guarantee*: Get your results within 4 working weeks from sample
receipt no waiting in uncertainty.

Carrier Screening & Trait Identification: Identify if you carry genetic conditions that may
affect future generations or inherited traits that influence your biology.

20% OFF Genetic Counseling: Access professional guidance to help you make sense of
your results and plan your next steps.

Clinical Grade Data: Your data meets diagnostic grade standards, suitable for use by
healthcare professionals in treatment decisions.

Genetic Risk for Inherited & Complex Diseases: Includes conditions like familial cancers, cardiomyopathies, neurological syndromes, and metabolic disorders.

    Carrier Status for Recessive Conditions: Useful for family planning, especially if you’re considering children.

      Drug Compatibility & Response (Pharmacogenomics): Discover how your DNA affects drug metabolism, dosage needs, and treatment risks.

        Health Optimization Based on Your DNA: Guidance on lifestyle, diet, supplements, and early interventions based on gene-level data.

        Understanding your exome and having personalized recommendations is beneficial for anyone interested in proactive and preventative healthcare. If you are curious about your genetic predispositions or want to optimize your health, this test can provide valuable insights:

        Patients with a family history of genetic conditions, individuals seeking clinical answers,
        physicians, or proactive health optimizers.

        Sample Type: Blood/Saliva

        Coverage: 100X Ultra Deep

        Turnaround Time: Less than 4 weeks *

        Includes: Detailed variant interpretation, clinical grade insights, and actionable health
        information

        • Full 100X Whole Exome Sequencing
        • Clinical-grade variant analysis (pathogenic, likely pathogenic, and VUS)
        • Carrier status, inherited condition screening
        • Turnaround Time GUARANTEED: Less than 4 weeks *
        • 20% OFF on Genetic Counseling
        • Personalized health reports available anytime **
        • Medically actionable variant reporting (based on ACMG guidelines)
        • Trait markers (e.g. metabolism, nutrient absorption, skin/hair traits)
        • Recommendations for further screening, lifestyle, or treatment