CLINICAL GENOMICS
Evidence-based clarity. Lifelong insights.
Streamline your diagnostic workflow with the only platform built for Sequence Once, Query Often® processes. Start with the targeted panel you need. Unlock the full exome whenever you need it.
Exome+® backbone, lifelong access
One sample. Instant digital reflexing.
AI-powered insights at scale
Continuous evidence and interpretation with Helix Wayfinder™.
Smarter than the sample
Real outcomes, millions of patients. Powered by Helix Research Network®.
Our Test Catalog
Hereditary cancer
Identify how your patient’s genetics may facilitate preventative interventions and early detection, as well as recognize at-risk family members.
11
tests
Hereditary cardiovascular
Guide diagnosis and management of cardiovascular disorders through your patient’s genetic insights.
18
tests
Pharmacogenomics
Determine optimal prescriptions by analyzing drug efficacy and side effect risk based on your patient’s genetic profile.
12
tests
Proactive screening
Reveal how your patient's genes could impact their health, enabling proactive monitoring and preventive care before conditions develop.
3
tests
Targeted analyses
Evaluate specific predefined genetic variants to determine your patient’s risk for known conditions and enable focused, personalized interventions.
2
tests
Carrier screening
Assess your patients' potential to pass on inheritable conditions and inform family planning discussions with insights into serious genetic disorders.
4
tests
Precision Diagnostics, Scalable Solutions
Our approach goes beyond traditional genetic testing. We offer a scalable platform that grows with your needs, whether you're an independent practice or a large health system.
Solving Today’s Questions. Charting Tomorrow’s Paths.
Our platform delivers more than genetic results—it provides actionable answers and insights analyzed with AI and collected through the Helix Research Network® (HRN). With real-world evidence at its core, flexible testing options, and the ability to unlock new insights from a single sample over time, we help providers and health systems in their efforts to advance care today while planning for tomorrow.
Powered by AI and Real-World Evidence
Our proprietary AI-enabled Clinical Interpretation engine, Helix Wayfinder™ incorporates real-world evidence collected through the Helix Research network to translate complex data into clinical insights for health system partners.
One Sample for Life
We sequence the full exome up front, so future clinical tests can be ordered, with patient consent, without the need for a new sample. In many cases, additional results can be returned within minutes—supporting proactive, personalized care as clinical questions evolve.
Flexible, Comprehensive Testing Options
Our menu includes both single-gene tests and focused panels, making it easy to tailor testing to individual patients or broader population health goals—all from one platform that grows with your needs.
Partnering for Genomic Integration Success
We work closely with healthcare providers to ensure smooth implementation and ongoing success of genomic diagnostics in clinical practice.
Tailored Implementation
We assess your specific needs and design an integration plan that aligns with your clinical goals and existing workflows.
Comprehensive Education
Our team provides thorough training and support, ensuring your staff is confident in interpreting and applying genomic insights.
Seamless EHR & Portal Options
We ensure genomic data is readily accessible for you how you want it, supporting informed decision-making at the point of care.
Ongoing Clinical Support
Our team of genetic experts is available for consultation, helping you navigate complex cases and maximize the utility of genomic information.
Built For The Future
Our AI-enabled framework is powering new frontiers in genomic medicine. We are also developing large language model (LLM) capabilities to capture more nuanced patient histories from health records, unlocking even greater precision in genetic association studies.
A Selection of Our Partners
