NOTE: There is an industry-wide shortage of Alflex TSU's. At this time, we can't guarantee shipping times. 
 
DNA Test Description:
The comprehensive beef profile is our most detailed beef profile available. The following traits & conditions are included.
 
1. Genomic Evaluation Traits:
• Tenderness
• Marbling
• Meat Quality
• Yield Grade
• Average Daily Gain (ADG)
• Fertility
• Fat Quality
 
2. Coat Color
 
3. Parentage Verification
(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 with this order.)
 
4. Comprehensive Disease Anlysis:
• Abortion (Embryonic Lethality) - Beef Breeds
• Achondrogenesis, type II
• Albinism
• Alpha Mannosidosis
• Anhidrotic ectodermal dysplasia
• Anhidrotic ectodermal dysplasia, EDAR-related
• Arthrogryposis
• 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) - Bulldog Dwarfism
• Citrullinemia
• Coat colour, albinism
• Coat colour, albinism, oculocutaneous type IV
• Congenital Muscular Dystonia I
• Congenital Muscular Dystonia II
• Congenital Myoclonus
• Crooked Tail Syndrome
• Deficiency of uridine monophosphate synthase
• Developmental Duplication (DD)
• Dwarfism, Angus
• Dwarfism, Fleckvieh
• Dystrophic Epidermolysis Bullosa
• Ehlers-Danlos syndrome, type VII (Dermatosparaxis)
• Epidermolysis bullosa, junctionalis, LAMA3-related
• 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
• Muscular hypertrophy (double muscling)
• Myasthenic syndrome, congenital, CHRNE-related
• Myostatin
• Neuronal ceroid lipofuscinosis, 5
• Osteogenesis imperfecta, type II, COL1A1-related
• Osteopetrosis with gingival hamartomas
• Paunch Calf Syndrome
• Perinatal weak calf syndrome
• Progressive degenerative myeloencephalopathy (Weaver syndrome)
• Protoporphyria
• Rat Tailed
• Retinitis pigmentosa 1
• RNF11 (Growth Retardation)
• Scurs, type 2
• Slick hair
• Sperm, short tail
• Spherocytosis
• Spinal Muscular Atrophy
• Susceptibility to spongiform encephalopathy (mad cow disease)
• Tibial Hemimelia
• Zinc deficiency-like syndrome
 
 
What you receive:
Online Genomic Evaluation
Detailed Genomic Evaluation Report 
Visual display showing Whole Herd Analysis 
Individual Animal Carrier Information