About MoleculeDx

We’re on a mission to make early liver cancer detection as routine as a cholesterol test.

 

Our Mission

Built Around One Uncomfortable Truth

Every year, over 30,000 Americans die from liver cancer. The majority of those deaths were potentially preventable — not because we lack treatment options, but because the cancers were found too late to treat.

MoleculeDx was founded to close this gap. We combined next-generation genomic sequencing with clinical-grade AI to create a blood test that’s simple enough for any at-risk patient to use, accurate enough for physicians to trust, and affordable enough for widespread adoption.

Our Fusion-detect™ platform doesn’t just screen — it catches cancers at the stage when treatment can still save lives.

The Science

Why Fusion Genes?

When liver cells become cancerous, they produce characteristic fusion gene events — chromosomal rearrangements that generate novel protein sequences. These are detectable in the blood years before a tumor is visible on imaging.

 

Fusion Gene Biomarkers

Our test identifies specific chromosomal fusion events in circulating tumor DNA — a molecular fingerprint that is highly specific to hepatocellular carcinoma.

AI Classification Engine

Our Fusion-detect™ AI is trained on 50,000+ clinical samples. It classifies results with 96.7% accuracy, removing the subjectivity that plagues many diagnostic tests.

CLIA-Certified Laboratory

All samples are processed in our CLIA-certified laboratory under strict federal standards. Every result is reviewed by a licensed clinical pathologist before release.

Ready to Take Control of Your Liver Health?

Booking takes 2 minutes. A phlebotomist can be at your door within 48 hours. Don’t wait for symptoms that may never come.

Are You at Risk?

Liver Cancer Risk Factors

You may benefit from regular liver cancer screening if you have one or more of these conditions.

The test screens for hepatocellular carcinoma (HCC) — the most common form of primary liver cancer. We analyze your blood for fusion gene biomarkers that are specific to early-stage liver cancer. These markers appear in the bloodstream significantly earlier than tumors become visible on ultrasound or CT scans.

The test requires only a standard venipuncture — the same blood draw you’d receive at any clinic or doctor’s office. It is not a biopsy. There’s no tissue removal, no surgery, and no imaging. Most people describe it as mild and brief. The certified phlebotomist comes to your home and the draw itself takes 5–10 minutes.
 
The Fusion-detect™ test achieves 96.7% overall accuracy, 94.2% sensitivity, and 98.1% specificity in clinical validation. A liver biopsy is considered definitive for diagnosis — but it is invasive, carries risks of bleeding and infection, and is not suitable as a screening tool. Our test is a screening tool that identifies patients who need further investigation. For a positive MoleculeDx result, we facilitate referral to a physician for confirmatory imaging or biopsy if warranted.
 
MoleculeDx is accepted by most major US insurers including UnitedHealth, Anthem/Blue Cross Blue Shield, Aetna, Cigna, Humana, and UPMC Health Plan. Medicare Advantage plans are also accepted. Coverage for cancer screening tests varies by plan and diagnosis code. Our team will verify your specific coverage for free before you book — contact us or check at booking.moleculedx.com.
 
Results are delivered digitally within 24 hours of sample receipt at our laboratory. You’ll receive a secure notification by email or SMS with access to your full clinical report. For results that require attention, a care coordinator will reach out to you directly within the same window to guide next steps.
 
A positive result does not mean you have cancer — it means biomarkers were detected that warrant further evaluation. Our care coordinator will contact you immediately to explain your results in plain language and help arrange follow-up imaging (typically an MRI or CT) and referral to a hepatologist or oncologist. We work with your existing providers or can refer you to UPMC specialists depending on your location.
 
Yes. Through our exclusive partnership with University of Pittsburgh Medical Center, patients can walk into any UPMC facility and request the MoleculeDx liver cancer screening test. UPMC physicians can also order it directly through UPMC’s Epic EHR system. Results are delivered within 24 hours and integrated directly into your UPMC health record.
 
We partner with Portamedic (portamedic.com) and Travalab (travalab.com) — two of the largest and most trusted mobile phlebotomy networks in the United States. All phlebotomists are nationally certified (CPT or equivalent) and undergo background checks and quality assurance training specific to MoleculeDx sample handling protocols.
 
No referral is required to book a self-pay test. However, insurance coverage typically requires an ordering physician. If you don’t have a primary care provider, our care coordinators can help connect you with a telemedicine physician who can provide the order — often within the same day.
 
At-home phlebotomy through Portamedic and Travalab is available across all 50 US states, though coverage in rural areas may require advance scheduling of 3–5 days. Walk-in testing is currently available exclusively at UPMC locations. We are actively expanding our clinical site network — check booking.moleculedx.com for your specific zip code coverage.