The Miracle of Life - Perfected.
Panacea GenomeScreen™ is the leading edge of Preimplantation Genetic Testing with Whole Genome Sequencing (PGT-WGS), combining PGT-A, PGT-M, and PGT-SR - and much, much more in one test. Exclusively from GenEmbryomics, our test detects both inherited and new mutations across 3,200+ critical genes.
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The Only Standard That Matters: A Healthy Family
Standard preimplantation genetic testing (PGT) helps identify embryos with the correct number of chromosomes, detecting abnormalities (aneuploidies) and partial changes (mosaicism) that could affect pregnancy success. But even with correct chromosome numbers, it misses the thousands of genetic diseases hidden within an embryo's DNA sequence.
A single genetic mutation can mean the difference between a healthy baby and a severe, lifelong disease. Today, 1 in 10 families face this tragic reality, struck by a genetic disease that slips through the cracks of current preimplantation testing.
It’s Time for a Better Way
Panacea GenomeScreen™ provides comprehensive genetic screening before pregnancy. Our advanced technology not only identifies chromosome abnormalities and mosaicism but also screens for inherited and new genetic mutations. We provide clear, understandable reports so patients, under guidance, can make informed decisions about which embryo has the lowest risks and the greatest chance for a healthy future.
Safeguarding The Future of Families
Our calling is to use genetics to transform uncertainty into trust, and statistics into clarity. From the start, we safeguard the futures of families and those undergoing IVF. This is the new standard of care that every IVF journey deserves. This is GenEmbryomics, supporting health and success, hand in hand.
Family Health, First – Always
Our mission is simple: to give patients the genetic insights they need to choose the healthiest embryo and their healthiest family. By pioneering comprehensive embryo screening, we aim to bring more certainty to the IVF process through whole genome sequencing (PGT-WGS*). We want to help start a child’s life in the best way possible, with the greatest likelihood of being free from preventable genetic diseases.
*For Research Use Only
Why Choose GenEmbryomics?
- Unmatched Detail: Whole genome sequencing with Panacea GenomeScreen™ sees what others miss—every mutation, every possibility.
- Trusted Expertise: We combine innovation with reliability, giving your lab the tools to deliver superior genetic screening to IVF clinicians and their patients.
- Future-Focused: We’re not just sequencing DNA; we’re shaping a healthier tomorrow.
How It Works
"At GenEmbryomics, we are redefining IVF with genomics, putting your health in your hands."
Dr. Nick Murphy
CEO, GenEmbryomics