Genomic solutions & clinical action
The insights that personalize care
Moving from reactive to predictive, our genomic sequencing solutions utilize the power of genomics to help inform clinical decisions in an easy and approachable way.
Why you should take action
of people have taken a health-risk genetic test¹
spend on adverse drug reactions annually²
emergency department visits each year due to adverse drug events³
cost of medical services for breast cancer in 2020⁴
Our genetic testing solutions
myPGx
This broad, at-home pharmacogenomics (PGx) solution analyzes an individual's DNA to identify variants that may affect their response to certain drugs.
myGeneticScreen
This 11 gene panel identifies genes that may increase the risk for certain cancers and cardiac conditions.
Who is this solution for?
Health plans
Harness the power of this member-centric solution to facilitate better healthcare for members
Employers
Offer competitive benefits to empower your workforce with health insights they can use for years to come
Public Sector
Transform your constituents healthcare experiences by empowering them with personalized care
Health Systems
Leverage key insights to guide your patient care by integrating our solutions into your existing EMR
What sets us apart?
State-of-the-art owned labs
With CLIA Certification and CAP accreditation, the LetsGetChecked labs operate with gold-standard quality practices on a global level. Ownership of our own Laboratory infrastructure fuels the freedom to design panels that are optimized for specific population needs.
Making genomics approachable
Genetic data can be overwhelming, but our roots lie in an unbeatable patient-centric experience that focuses on education and engagement, driving results by empowering patients and providers.
Targeted engagement strategies
Expert-led online education hub
All-in-one secure patient portal
Configurable program design to achieve your goals
Our technology makes it easy to integrate our solution into your existing program infrastructure.
Real-time reporting portal
Powerful data visualizations
API technology
End-to-end care services to drive action
We have designed a solution to help patients and providers understand the next best steps to take post-result.
Counselling services from genetic experts
Regular screening plans for those who need closer monitoring
Clinical decision support
Pharmacy services to put pharmacogenomic insights into action
Dr. Avni Santani
Chief Genomics Officer
Dr. Robert Mordkin, MD
Chief Medical Officer
Dr. Kate Karfilis
Director of Product - Genomics
Michael Rummel
Chief Laboratory Officer
Request a demo
Learn more about our solution suite
myPGx
Genetic variations influence how we react to medications, which can lead to reduced efficacy and adverse side effects. This broad at-home PGx solution identifies potential drug-gene interactions for 100+ drugs across three major disease categories, representing 1 billion prescriptions, annually.
Behavioral health, pain, and cardiovascular drugs
Patient-friendly test and experience
Clinical decision support
myGeneticScreen
Our proactive screening test determines genetic risk for the most common hereditary conditions, enabling patients and their families to take preventative measures and facilitate early detection.
Hereditary Breast and Ovarian Cancer Syndrome, Lynch Syndrome, and Familial Hypercholesterolemia
Pre- and post-genetic counseling
Family member testing
Follow-up screening services for cholesterol
A simple patient experience
At-home sample collection
Simple saliva sample kits sent to the home and returned to our lab
Genetics education hub
Empower & inform with our expert-led information hub
Result report delivery
Online through their secure dashboard for easy access
Counselling services
Access to experts to better understand results
Clinical decision support
Guidance for HCPs from genetic experts
Related articles
The Human Genome Project and Pharmacogenomics
How PGx testing can help improve outcomes in patients with depression
Potential Cost Savings By Preventing Adverse Drug Events