Thoroughbred VGNome™ BLACK
A DNA Check-up
From diagnosing genetic disease to getting a clean bill of health
Or identifying healthy horses that could pass diseases to their foal
VGnome does it all
Comprehensive testing. Expertise you can trust
Victory Genomics
Certified Health
Whether for registration, breeding, or peace of mind, Victory Genomics can certify your horse free of any inherited genetic disease. We also tell you if your horse carries the mutation for a disease and the chances of passing it on.
Testing by Breed
It’s in the Bloodline
Different breeds are prone to different diseases. Get relevant results tailored for your horse. Or test for all diseases if you’re planning to crossbreed or suspect your horse isn’t purebred.
Inheriting Disease
Shake off Illness!
“Prevention is better than cure”. Make informed breeding choices to reduce or even negate the likelihood of an ill foal. Have a desirable bloodline. Stamp out disease.
Diagnosis
Mysterious Symptoms?
Explain the enigma with VGnome. When your horse has unexplained symptoms and no firm diagnosis, VG-Health can rule in, or rule out, common inherited diseases, guiding your vet. Early intervention often equals improved prognosis, treatment, and quality of life.
Still no diagnosis?
Engage with Victory Genomics for custom disease discovery.
Our Tests
Down with Disease
Awesome Arabians
Test for the four most common inherited diseases in Arabians. Arabian breed associations across the world recommend testing for these diseases.
Find out whether your Arabian carries the genetic mutations that can cause disease. Then, make smart breeding choices to protect the next generation of Arabian foals.
| Cerebellar abiotrophy | Lavender foal syndrome |
| Occipitoatlantoaxial malformation | Severe combined immunodeficiency disease |
Precious Thoroughbreds
Our comprehensive inherited genetic disease panel geared toward Thoroughbreds. Testing for these conditions can guide diagnosis of mysterious symptoms, determine genetic disease, and inform breeding choices.
| Androgen insensitivity syndrome | Cerebellar abiotrophy |
| Hereditary equine regional dermal asthenia | Hoof wall separation syndrome |
| Hydrocephalus | Hyperkalemic periodic paralysis |
| Immune‐mediated myositis | Malignant hyperthermia |
| Myotonia | Ocular squamous cell carcinoma |
| Overo Lethal White Syndrome | Warmblood fragile foal syndrome |
All-breed Disease Panel
Our complete test for inherited genetic diseases across all breeds for total peace of mind. Useful for cross breeds or when considering a cross breed.
| Androgen insensitivity syndrome | Cerebellar abiotrophy |
| Dwarfism, ACAN | Dwarfism, Friesian |
| Foal immunodeficiency syndrome | Glycogen branching enzyme deficiency |
| Hereditary equine regional dermal asthenia | Hoof wall separation syndrome |
| Hydrocephalus | Hyperkalemic periodic paralysis |
| Immune‐mediated myositis | Incontinentia Pigmenti |
| Junctional epidermolysis bullosa (JEB1) | Junctional epidermolysis bullosa (JEB2) |
| Lavender Foal Syndrome | Malignant hyperthermia |
| Myotonia | Naked foal syndrome |
| Occipitoatlantoaxial malformation | Ocular squamous cell carcinoma |
| Overo Lethal White Syndrome | Polysaccharide storage myopathy |
| Severe combined immunodeficiency disease | Warmblood fragile foal syndrome |
| Multiple Congenital Ocular Anomalies |
