What's Included:
Parentage verification
Tenderness & Marbling
Complete genetic defects analysis.
Coat Color
1 Year DNA banking
Parentage Verification
Use parentage verification to confirm your breeding records. When requesting parentage test, verify that all possible parents have been genotyped by Resero Genomics prior to sample submission. If parents have not been genotyped, please include parent samples when placing an order.
Coat Color
Accurately determine the coat color genotopes for your anmals.
DNA Storage:
Store and protect your DNA in our safe-secure storage center. When you store your DNA with Resero, your DNA may be withdrawn and used for genetic testing when you are ready, or transferred to any lab of your choosing. Note: only tissue samples can be used for DNA banking.
Genetic Defects:
Make more informed breeding decisions. With Resero's comprehensive genetic defects analysis, you can reduce & eliminate genetic disorders / diseases from your herd.
Conditions Tested:
- Abortion (Embryonic Lethality)
- Achondrogenesis, type II
- Alpha Mannosidosis
- Anhidrotic ectodermal dysplasia
- Anhidrotic ectodermal dysplasia, EDAR-related
- Arthrogryposis Multiplex
- Arthrogryposis Multiplex (AM)
- Arthrogryposis, lethal syndrome
- Axonopathy
- Beta Mannosidosis
- Bovine Arachnomelia Syndrome
- Bovine Leukocyte Adhesion Deficiency (BLAD)
- Bovine Spongiform Encephalopathy (BSE)
- Briskets Disease (High Altitude Sickness)
- Caprine-like Generalized Hypoplasia Syndrome
- Cardiomyopathy and woolly haircoat syndrome
- Chediak-Higashi syndrome
- Chondrodysplasia (5 Mutations)
- Citrullinemia
- Coat Colour Dilution
- Coat colour, albinism
- Coat colour, albinism, oculocutaneous type IV
- Congenital Muscular Dystonia I
- Congenital Muscular Dystonia II
- Congenital Myoclonus
- Contractual Arachnodactyly
- Crooked Tail Syndrome
- Developmental Duplication (DD)
- Dwarfism, Angus
- Dwarfism, Fleckvieh
- Dystrophic Epidermolysis Bullosa
- Ehlers-Danlos syndrome, type VII
- Epidermolysis bullosa, dystrophic
- Factor XI deficiency
- Fanconi syndrome
- Fleckvieh Haplotype 4 (FH4)
- Forelimb-girdle muscular anomaly
- German White Fleckvieh Syndrome
- Glycogen storage disease II
- Glycogen storage disease V
- Goitre, familial
- Hemophilia A
- Hydrallantois
- Hypotrichosis
- Hypotrichosis, KRT71-related
- Hypotrichosis, streaked
- Ichthyosis congenita
- Male subfertility
- Maple Syrup Urine Disease
- Marfan syndrome
- Mulefoot
- Multiple ocular defects
- Myasthenic syndrome, congenital
- Myostatin
- Neuronal ceroid lipofuscinosis, 5
- Neuropathic Hydrocephalus
- Oculocutaneous Hypopigmentation
- Osteogenesis imperfecta, type II
- Osteopetrosis
- Osteopetrosis w/ gingival hamartomas
- Paunch Calf Syndrome
- Perinatal weak calf syndrome
- Protoporphyria
- Pseudomyotonia
- Pulmonary Hypoplasia w/ Anasarca
- Rat Tailed
- Retinitis pigmentosa 1
- RNF11 Growth Retardation
- Slick hair
- Sperm, short tail
- Spherocytosis
- Spinal Muscular Atrophy
- Susceptibility to Spongiform encephalopathy (Mad Cow Disease)
- Tibial Hemimelia
- Weaver syndrome
- Zinc deficiency-like syndrome
Additional Terms and Conditions
For parentage verification, both parents and offspring need to be tested for correct match. Any samples requiring parentage verification, ensure samples from parent(s) / offspring are submitted for testing.
Only DNA extracted from tissue samples can be banked. Hair samples don't provide sufficient DNA for long term DNA storage.