Exo-TEK™ analyzes all protein-coding regions of the genome (the exome). By focusing on the genes where the vast majority of disease-causing mutations occur, Exo-TEK™ serves as a powerful diagnostic tool for complex medical cases and carrier screening.
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Patients with complex, undiagnosed symptoms or conditions.
Children with unexplained developmental delays or intellectual disabilities.
Individuals suspected of having rare genetic disorders.
Prospective parents looking to identify carrier status for hereditary conditions before or during pregnancy.
Precision Focus: Targeting the 1–2% of the genome responsible for ~85% of known disease-causing variants, delivering high diagnostic yield for rare disorders.
Clinic-Led Customization: Clinics can customize analysis parameters or focus on specific gene subsets to align with their clinical needs and patient population.
Diagnostic Clarity: Designed to identify pathogenic and novel variants that standard targeted panels often miss.
Exo-TEK™ is a high-yield diagnostic tool for rare and undiagnosed conditions. To get the most out of exome sequencing in your clinic, consider:
Standardized Phenotype Documentation: Accurate, detailed phenotyping significantly improves variant prioritization and interpretation.
Established Counseling Protocols: A formal pre-test counseling protocol ensures patients understand the test’s full scope, including potential incidental findings.
Specialist Referral Pathways: Pre-defined referral pathways support patients who receive complex or pathogenic results.
Periodic Data Reanalysis: Reanalyzing exome data every 1–2 years can yield new answers as medical knowledge continues to evolve.
A simple, guided process from consultation to clinically actionable reporting.
Contact our team to learn how our tests can enhance your clinical offerings and improve patient outcomes.
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