Genetic insights for informed healthcare decisions
Helix provides you and your healthcare provider with advanced genetic insights to support more personalized care. Our comprehensive genetic testing services offer a deeper understanding of your health, enabling more informed decisions and proactive health management strategies.
Get in TouchComprehensive genetic testing, simplified
At Helix, we’re dedicated to making genetic insights accessible and actionable. Our state-of-the-art sequencing technology and innovative Sequence Once, Query Often® approach allow for a wide range of genetic tests from a single sample. This means you can gain valuable health information over time without repeated sample collection. Whether you’re exploring hereditary cancer risks, heart health, medication responses, or family planning, Helix provides the tools to support your healthcare journey.
Diagnostic Testing Patient Resources
Informed Consent for Helix Diagnostic Testing
DownloadInformed Consent for Helix Pharmacogenomics
DownloadHereditary Cancer Patient Brochure
DownloadCardiovascular Disease Patient Brochure
DownloadPharmacogenomics Patient Brochure
DownloadProactive Screening Patient Brochure
DownloadSpecimen Requirements
DownloadSpecimen Collection Instructions
Read moreResult Guides
Read moreCancer and Cardiology Diagnostic Pre-test Education Video
Watch NowCarrier Screening Pre-test Education Video
Watch NowCarrier Screening Patient Brochure
DownloadHow it works
From consultation to actionable results — genetic testing in five simple steps.
Consult Your Provider
Discuss if genetic testing is right for you.
Easy Ordering
Your provider can order tests directly.
Simple Sample Collection
Provide a saliva or blood sample.
Comprehensive Analysis
We analyze your sample using advanced sequencing.
Actionable Results
Receive insights to guide your healthcare decisions.
Comprehensive Test Menu
A comprehensive, clinically validated testing menu — all accessible from a single platform.
Hereditary Cancer
BRCA1/2, Lynch syndrome, and comprehensive multi-gene panels for hereditary cancer risk identification and cascade screening.
Cardiovascular Genomics
Familial hypercholesterolemia, cardiomyopathy, arrhythmia syndromes, and aortopathy panels for proactive cardiac care.
Pharmacogenomics (PGx)
Drug-gene interaction testing to optimize medication selection and dosing — with results in minutes via Sequence Once, Query Often®.
Carrier Screening
Expanded carrier screening for reproductive planning, covering hundreds of autosomal recessive and X-linked conditions.
Proactive Screening
Population-scale genomic screening programs that identify at-risk patients before symptoms appear — driving early intervention and better outcomes.
Targeted Analyses
Evaluate specific predefined variants to determine your risk for known conditions and enable focused, personalized interventions.
Frequently Asked Questions (FAQs)
Answers for patients who have questions about diagnostic testing.