Get more answers with whole genome testing

 

Whole genome-based testing is the fastest way to reach a clear diagnostic outcome, but not all genome tests are equal. You can trust our clinical experts, working with our advanced technology, to find the answers your patients need.

Watch the video below to see how we solved a challenging case of Segawa syndrome – after it was missed by traditional tests.

Our areas of testing

Genetic Disorders

We see more, so you know more. Find out why our Genomic Unity^® portfolio of tests offers the highest chance of finding an answer for conditions that occur from infancy through adulthood.

Reproductive Genetics

Get more genetic answers in the reproductive journey. Learn how our IriSight^® portfolio of tests provides comprehensive diagnostic information for fetal anomalies identified during pregnancy or following pregnancy loss.

Precision Oncology

Get comprehensive cancer insights. Explore precision testing for assessment of cancer predisposition and cancer treatment optimization with our OncoAlly^® portfolio of tests.

Wellness Testing

Help your patients understand their genetic risks. Learn about clinical grade testing with our Genomic Inform^® predictive screening test, available for healthy adults 18 years of age or older.

Resources for your practice

Billing Information

We know cost is an important factor when considering genetic testing. Learn about our commitment to transparent pricing, billing options and access to assistance programs for patients.

Forms

Visit our Forms page for quick access to everything you’ll need for ordering testing, gaining access to raw sequencing data and sharing test results with external providers.

Specimen Requirements

We accept a variety of sample types, depending on the test ordered. Access technical information for each here.

Understanding Variantyx Reports

Variantyx diagnostic reports detail genetic findings that correlate with a patient’s clinical presentation. Browse and download a sample report to learn about key sections.

ACMG Secondary and Other Actionable Findings

When a patient has broad genetic testing, they have the option to learn about variants that put them at risk for other conditions. Learn about our reporting policies for these types of actionable findings.

FAQs

You’ve got questions, we have answers. Explore our library of frequently asked questions. Don’t see what you’re looking for? Reach us via our Contact Us page.

See our testing in action

We’re proud of the role we play in providing diagnoses for many patients and their families.  Browse our library of representative cases to see some of the unique variants we’re able to detect with our technology – oftentimes after they were missed by prior genetic testing.