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CONTACT

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The best care of
your patients is in their DNA

Genetic analyses created by veterinarians for the personalised care of your furry friends.

 

DNA Samples

Blood sample in EDTA tubes.

In specific cases, we also send saliva kits to the veterinary centre for sample collection. The kits are very simple to use, and are designed specifically for collecting and preserving DNA samples..

Science

We isolate and process the DNA using the most advanced genomic technology.

Thanks to this, we offer you recommendations that improve the quality of life of your patients.

Support

We send you a report with the results and recommendations for personalising the treatment of each patients.

Additionally, you can always request further support after receiving the results.

GenTest

genomics analysis for your patients

Genetic screening identifies potential health risks and allows veterinarians and pet owners to improve and extend the quality of life of patients, both preventively and curatively.

Support

If you have any questions, contact our experts at info@omicabiomed.com. We will be delighted to help you.

Time

 Time is important for everyone. We deliver results within 15 days from when the samples arrive at our lab

Results

In the GenTest reports, the results are detailed in a user friendly format, easy to interpret for pet owners.

Functionals Gentic Panels

Functional panels, we group breeds phylogenetically, optimising costs to offer you only what you need at a unique price. Exclusively for sale to veterinarians.

CANINE GENTEST 1

General panel with the 10 most common diseases in dogs.

14 common diseases in Breeds Group 1.

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Diseases

General Panel diseases:

  • Exercise Induced Collapse (EIC)
  • Factor VII Deficiency
  • Chondrodysplasia
  • Degenerative Myelopathy (DM)
  • Hyperuricosuria (SLC)
  • Malignant Hyperthermia (MH)
  • Primary Lens Luxation (PLL)
  • Progressive Retinal Atrophy (prcd-PRA)
  • MDR1 – Multi-Drug Resistance
  • Von Willebrand Disease Type I (VWD1

Breed group diseases

  • Copper Toxicosis
  • Type IA Cystinuria
  • Hereditary Nasal Parakeratosis (HNPK)
  • Narcolepsy
  • Degenerative Myelopathy 2 (DM2)
  • Stargardt Disease (STGD-PRA)
  • Primary Open Angle Glaucoma (POAG)
  • Gallbladder Mucocele
  • Familial Nephropathy
  • Skeletal Dysplasia 2 (SD2)
  • Pyruvate Kinase Deficiency (DPK)
  • Intestinal Cobalamin Malabsorption (Beagle)
  • Mast Cell Tumor Risk
  • Osteosarcoma Risk
Breeds

Group 1

    • American Cocker Spaniel
    • Basset Hound
    • Beagle
    • Hound
    • Petit Basset Griffon Vendéen (PBGV)
    • Dachshund (Teckel)
    • Dalmatian
    • Bernese Mountain Dog
    • English Cocker Spaniel
    • English Springer Spaniel
    • Cavalier King Charles Spaniel
    • Irish Water Spaniel
    • Brittany Spaniel
    • German Shorthaired Pointer
    • Great Dane
    • Rottweiler
    • Flat-coated Retriever
    • Golden Retriever
    • Labrador Retriever
    • Newfoundland
    • Borzoi
    • Scottish Deerhound
    • Irish Wolfhound
    • Greyhound
    • Sighthound (Lebrel)
    • Italian Greyhound
    • Ibizan Hound
    • Azawakh
Extra diseases

Extra diseases 1, 2, 3

 

 

CANINE GENTEST 2

General panel with the 10 most common diseases in dogs.

12 common diseases in Breeds Group 2.

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Diseases

General Panel diseases

  • Exercise Induced Collapse (EIC)
  • Factor VII Deficiency
  • Chondrodysplasia
  • Degenerative Myelopathy (DM)
  • Hyperuricosuria (SLC)
  • Malignant Hyperthermia (MH)
  • Primary Lens Luxation (PLL)
  • Progressive Retinal Atrophy (prcd-PRA)
  • MDR1 – Multi-Drug Resistance
  • Von Willebrand Disease Type I (VWD1)

 Breed group diseases

  • Progressive Retinal Atrophy (crd2-PRA)
  • Multifocal Retinopathy (CMR1,2,3)
  • Achromatopsia (day blindness) (ACHM1)
  • Collie Eye Anomaly (CEA)
  • Type 3 Cystinuria
  • Hemophilia A 1, 2 (Factor VIII)
  • Hemophilia B
  • Ichthyosis (SLC27A4, ASPRV1)
  • Primary Ciliary Dyskinesia
  • Intestinal Cobalamin Malabsorption (Collie)
  • Congenital Myotonia
  • Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND)
Breeds

Breeds of the group 2

  • Doberman Pinscher
  • Giant Schnauzer
  • Standard Schnauzer
  • German Shepherd
  • Portuguese Water Dog
  • Austrian Pinscher
  • Beauceron
  • Boston Terrier
  • Boxer
  • French Bulldog
  • Miniature Bull Terrier
  • Staffordshire Bull Terrier
  • Glen of Imaal Terrier
  • Bullmastiff
  • English Mastiff
  • American Pit Bull Terrier
  • Belgian Shepherd (Belgian Malinois is one common type)
  • Australian Shepherd
  • Collie
  • Shetland Sheepdog
  • Border Collie
  • Cardigan Welsh Corgi
  • Pembroke Welsh Corgi
  • Old English Sheepdog
  • Australian Cattle Dog
Extra diseases
Extra diseases

1, 2, 3

CANINE GENTEST 3

General panel with the 10 most common diseases in dogs.

11 common disease in the breed en el grupo 3

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Que este elemento del acordeón esté oculto permite que todos los elementos se vean cerrados. La otra alternativa implicaba incluir código javascript y esta me ha parecido más sencilla.

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https://help.elegantthemes.com/en/articles/4748294-make-divi-accordions-closed-by-default

Diseases

 General panel diseases

  • Exercise Induced Collapse (EIC)
  • Factor VII Deficiency
  • Chondrodysplasia
  • Degenerative Myelopathy (DM)
  • Hyperuricosuria (SLC)
  • Malignant Hyperthermia (MH)
  • Primary Lens Luxation (PLL)
  • Progressive Retinal Atrophy (prcd-PRA)
  • MDR1 – Multi-Drug Resistance
  • Von Willebrand Disease Type I (VWD1)

Breed group diseases

  • Pyruvate Kinase Deficiency (DPK)
  • Craniomandibular Osteopathy (CMO)
  • Van den Ende-Gupta Syndrome (VDEGS)
  • Congenital Hypothyroidism with Goiter (CHG)
  • Spinocerebellar Ataxia (SCA)
  • Neuronal Ceroid Lipofuscinosis (NCL4A)
  • Polyneuropathy with Ocular Abnormalities (POANV)
  • Polycystic Kidney Disease
  • Palmoplantar Hyperkeratosis
  • X-linked Nephritis
  • Myotonia
Breeds

Breeds of the group 3

  • Basenji
  • Akita
  • Chow Chow
  • Dingo
  • Shar Pei
  • Alaskan Malamute
  • Siberian Husky
  • Afghan Hound
  • Saluki
  • American Eskimo Dog
  • Samoyed
  • Pomeranian
  • Chihuahua
  • Pekingese
  • Shih Tzu
  • Brussels Griffon
  • Pug
  • Papillon
  • Miniature Pinscher
  • Havanese
  • Standard Poodle
  • Toy Poodle
  • Jack Russell Terrier
  • Briard
  • Australian Terrier
  • Yorkshire Terrier
  • Cairn Terrier
  • West Highland White Terrier
  • Scottish Terrier
  • Norwich Terrier
Extra diseases
Extra diseases

1, 2, 3

OMIBREED

More than 460,000 markers that allow us to personalize genotyping studies, such as breed purity  ancestry and other conditions.etc..

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Traits

 

Gene Symbol Gene Name OMIA Number Trait
TYRP1 tyrosinase-related protein 1 001249 Coat colour, brown
T T brachyury transcription factor 000975 Tail, short
ASIP aspartic peptidase, retroviral-like 1 000201 Coat colour, agouti
ASIP aspartic peptidase, retroviral-like 1 000201 Coat colour, agouti
MLPH melanophilin 000031 Alopecia, colour mutant
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) 001199 Coat colour, extension
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) 001199, 001495 Coat colour, grizzle, Coat colour, extension
CBD103 beta-defensin 103 001416 Coat colour, dominant black
PSMB7 proteasome subunit beta 7 001454 Coat colour, harlequin
KRT71 keratin 71, type II 000245 Curly coat
MLPH melanophilin 000031 Coat colour, dilute
CBD103 beta-defensin 103 001416 Coat colour, dominant black
FGF5 fibroblast growth factor 5 000439 Hair, long
FGF5 fibroblast growth factor 5 000439 Hair, long
FGF5 fibroblast growth factor 5 000439 Hair, long
RSPO2 R-spondin 2 001498 Improper coat
FGF5 fibroblast growth factor 5 000439 Hair length
TYRP1 tyrosinase-related protein 1 001249 Coat colour, brown
TYRP1 tyrosinase-related protein 1 001249 Coat colour, brown
KIT KIT proto-oncogene receptor tyrosine kinase 001737 Coat colour, white spotting, KIT-related
Diseases

Enfermedades

Gene Symbol Gene Name OMIA Number Disease
CNGB1 cyclic nucleotide gated channel beta 1 000830 Progressive retinal atrophy
ENAM enamelin 001805 Amelogenesis imperfecta
SEL1L sel-1 suppressor of lin-12-like (C. elegans) 001692 Ataxia, cerebellar, progressive early-onset
LGI2 leucine-rich repeat LGI family, member 2 001596 Epilepsy, benign familial juvenile
C3 complement component 3 000155 C3 deficiency
ARSG arylsulfatase G 001503 Neuronal ceroid lipofuscinosis, 4A
ATP1B2 ATPase, Na+/K+ transporting, beta 2 polypeptide 002110 Ataxia, cerebellar, ATP1B2-related
CNGB3 cyclic nucleotide gated channel beta 3 001676 Achromatopsia (cone degeneration, hemeralopia), GSPT
VLDLR very low density lipoprotein receptor 001947 Cerebellar hypoplasia, VLDLR-associated
MUTYH mutY DNA glycosylase 000175 Cerebellar abiotrophy
SDCA1 / ATP1B2 Ataxia, cerebellar, ATP1B2-related 002110 Ataxia, cerebellar, ATP1B2-related
SNX14 sorting nexin 14 002034 Cerebellar cortical degeneration, Hungarian Vizsla
TPO thyroid peroxidase 000536 Hypothyroidism
ITGA10 integrin, alpha 10 001886 Chondrodysplasia, disproportionate short-limbed
CCDC39 coiled-coil domain containing 39 001540 Ciliary dyskinesia, primary
CLN5 ceroid-lipofuscinosis, neuronal 5 001482 Neuronal ceroid lipofuscinosis, 5
ITGB2 integrin subunit beta 2 000595 Leukocyte adhesion deficiency, type I
FERMT3 fermitin family member 3 001525 Leukocyte adhesion deficiency, type III
BEST1 bestrophin 1 001444 Multifocal retinopathy 1
BEST1 bestrophin 1 001553 Multifocal retinopathy 2
ATP7A ATPase, Cu++ transporting, alpha polypeptide 000640 Menkes disease
ATP7B ATPase, Cu++ transporting, beta polypeptide 001071 Wilson disease
SLC37A2 solute carrier family 37 (glucose-6-phosphate transporter), member 2 000236 Craniomandibular osteopathy
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta 001674 Cone-rod dystrophy 1
IQCB1 IQ motif containing B1 001675 Cone-rod dystrophy 2
RPE65 retinal pigment epithelium-specific protein 65kDa 001222 Leber congenital amaurosis (congenital stationary night blindness)
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1 000256 Cystinuria, type I – A
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1 001879 Cystinuria, type II – A
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1 001879 Cystinuria, type II – A
SLC7A9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 001880 Cystinuria, type II – B
FAM20C family with sequence similarity 20, member C 002015 Dental hypomineralization
FLCN folliculin 001335 Renal cystadenocarcinoma and nodular dermatofibrosis
BEST1 bestrophin 1 001554 Multifocal retinopathy 3
BEST1 bestrophin 1 001554 Multifocal retinopathy 3
ADAM9 ADAM metallopeptidase domain 9 001520 Cone-rod dystrophy 3
SOD1 superoxide dismutase 1, soluble 000263 Degenerative myelopathy
GLB1 galactosidase, beta 1 000402 Gangliosidosis, GM1 (Alaskan Husky)
GLB1 galactosidase, beta 1 000402 Gangliosidosis, GM1 (Gangliosidosis_PWD)
GAA glucosidase, alpha; acid 000419 Glycogen storage disease II
F9 coagulation factor IX 000438 Haemophilia B
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4 001973 Ichthyosis, SLC27A4-related
AMHR2 anti-Mullerian hormone receptor, type II 000791 Persistent Mullerian duct syndrome
ATP13A2 ATPase type 13A2 001552 Neuronal ceroid lipofuscinosis, 12
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant 001443 Neuronal ceroid lipofuscinosis, 6
PDE6A phosphodiesterase 6A, cGMP-specific, rod, alpha 001314 Rod-cone dysplasia 3
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10 : [variant c.627C>G] 002089 Ataxia, cerebellar, KCNJ10-related
F7 coagulation factor VII (serum prothrombin conversion accelerator) 000361 Factor VII deficiency
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4 001524 Gallbladder mucoceles
GALC galactosylceramidase 000578 Krabbe disease
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10 001870 Glaucoma, primary open angle, ADAMTS10-related
G6PC glucose-6-phosphatase, catalytic subunit 000418 Glycogen storage disease Ia
GLB1 galactosidase, beta 1 000402 Gangliosidosis, GM1
HEXB hexosaminidase B (beta polypeptide) 001462 Gangliosidosis, GM2, type II
DMD Duchenne muscular dystrophy 001081 Muscular dystrophy, Duchenne type
TTC8 tetratricopeptide repeat domain 8 001984 Golden Retriever PRA 2
AGL amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase 001577 Glycogen storage disease IIIa
CNGB1 cyclic nucleotide gated channel beta 1 000830 Progressive retinal atrophy
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4 001973 Ichthyosis, SLC27A4-related
ARHGEF10 Rho guanine nucleotide exchange factor (GEF) 10 001917 Polyneuropathy, ARHGEF10-related
COL1A1 collagen, type I, alpha 1 002126 Osteogenesis imperfecta, type III, COL1A1-related
ASPRV1 aspartic peptidase, retroviral-like 1 002099 Ichthyosis, ASPRV1-related
FOXI3 forkhead box I3 000323 Ectodermal dysplasia
CNGA3 cyclic nucleotide gated channel alpha 3 001481 Achromatopsia-2
CNGB3 cyclic nucleotide gated channel beta 3 001365 Achromatopsia (cone degeneration, hemeralopia), AMAL
CNGA1 cyclic nucleotide gated channel alpha 1 001977 Progressive retinal atrophy, CNGA1-related
ANO6 anoctamin 6 001353 Scott Syndrome
LHX3 LIM homeobox 3 000307 Dwarfism, pituitary
PKD1 polycystic kidney disease 1 (autosomal dominant) 000807 Polycystic kidney disease
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9 001033 Urolithiasis
CAT catalase 001138 Hypocatalasia
FAM83G family with sequence similarity 83, member G 001327 Hyperkeratosis, palmoplantar
KRT10 keratin 10, type I 001415 Hyperkeratosis, epidermolytic
FNIP2 folliculin interacting protein 2 000526 Hypomyelination of the central nervous system
CUBN cubilin (intrinsic factor-cobalamin receptor) 001786 Intestinal cobalamin malabsorption, CUBN-related
CUBN cubilin (intrinsic factor-cobalamin receptor) 001786 Intestinal cobalamin malabsorption, CUBN-related
RAB3GAP1 RAB3 GTPase activating protein subunit 1 (catalytic) 001970 Polyneuropathy, RAB3GAP1-related
L2HGDH L-2-hydroxyglutarate dehydrogenase 001371 L-2-hydroxyglutaricacidemia
LOC489707 carbohydrate sulfotransferase 6 002071 Macular corneal dystrophy
CLCN1 chloride channel, voltage-sensitive 1 000698 Myotonia
DMD Duchenne muscular dystrophy 001081 Muscular dystrophy, Duchenne type
GUSB glucuronidase, beta 000667 Mucopolysaccharidosis VII
SGSH N-sulfoglucosamine sulfohydrolase 001309 Mucopolysaccharidosis IIIa
GUSB glucuronidase, beta: “missense mutation (c.866C>T) causing a pathogenic p.P289L change in a conserved functional domain of β-glucuronidase (GUSB)” 000667 Mucopolysaccharidosis VII
MSTN myostatin 000683 Muscular hypertrophy (double muscling)
ADAMTSL2 ADAMTS-like 2 001509 Musladin-Lueke syndrome
CHAT choline O-acetyltransferase 002072 Myasthenic syndrome, congenital
CLCN1 chloride channel, voltage-sensitive 1 000698 Myotonia
BIN1 bridging integrator 1 001660 Myopathy, Great Dane
MTM1 myotubularin 1 001508 Myotubular myopathy 1
HCRTR2 hypocretin (orexin) receptor 2 000703 Narcolepsy
HCRTR2 hypocretin (orexin) receptor 2 000703 Narcolepsy
PPT1 palmitoyl-protein thioesterase 1 001504 Neuronal ceroid lipofuscinosis, 1
CTSD cathepsin D 001505 Neuronal ceroid lipofuscinosis, 10
CLN8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) 001506 Neuronal ceroid lipofuscinosis, 8
ATF2 activating transcription factor 2 001471 Neonatal encephalopathy with seizures
COL4A5 collagen, type IV, alpha 5 001112 Nephritis, X-linked
MFN2 mitofusin 2 002153 Neuroaxonal dystrophy
COL1A2 collagen, type I, alpha 2 002112 Osteogenesis Imperfecta
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1) 001483 Osteogenesis imperfecta_Dachshund Osteogenesis imperfecta, SERPINH1-related
P2RY12 purinergic receptor P2Y, G-protein coupled, 12 001564 Bleeding disorder due to P2RY12 defect
PDP1 pyruvate dehyrogenase phosphatase catalytic subunit 1 001406 Pyruvate dehydrogenase deficiency
PFKM phosphofructokinase, muscle 000421 Glycogen storage disease VII
PKLR pyruvate kinase, liver and RBC 000844 Pyruvate kinase deficiency of erythrocyte
PKLR pyruvate kinase, liver and RBC 000844 Pyruvate kinase deficiency of erythrocyte
PKLR pyruvate kinase, liver and RBC 000844 Pyruvate kinase deficiency of erythrocyte
ADAMTS17 ADAM metallopeptidase with thrombospondin type 1 motif, 17 000588 Lens luxation
NDRG1 N-myc downstream regulated 1 002120 Polyneuropathy
ADAMTS17 ADAM metallopeptidase with thrombospondin type 1 motif, 17 001976 Glaucoma
JAK2 Janus kinase 2 000809 Polycythemia
NDRG1 N-myc downstream regulated 1 002120 Polyneuropathy, NDRG1-related
SAG S-antigen; retina and pineal gland (arrestin) 001876 Progressive retinal atrophy, Basenji
KLKB1 kallikrein B, plasma (Fletcher factor) 1 000819 Prekallikrein deficiency
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta 001669 Rod-cone dysplasia 1a
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta 000882 Rod-cone dysplasia 1
COL7A1 collagen, type VII, alpha 1 000341 Epidermolysis bullosa, dystrophic
RAG1 recombination activating gene 1 001574 Severe combined immunodeficiency disease, autosomal, T cell-negative, B cell-negative, NK cell-positive
COL11A2 collagen, type XI, alpha 2 001772 Skeletal dysplasia 2 (SD2)
PRKDC protein kinase, DNA-activated, catalytic polypeptide 000220 Severe combined immunodeficiency disease, autosomal
SMOC2 SPARC related modular calcium binding 2 001551 Brachycephaly
CAPN1 calpain 1, (mu/I) large subunit 001820 Ataxia, spinocerebellar, CAPN1-related
TGM1 transglutaminase 1 000546 Ichthyosis, Golden Retriever   Ichthyosis, TGM1-related
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41) 001000 Thrombasthenia
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41) 001000 Thrombasthenia
TUBB1 tubulin, beta 1 class VI 001001 Thrombocytopaenia
RASGRP1 RAS guanyl releasing protein 1 (calcium and DAG-regulated) 001003 Thrombopathia
RASGRP1 RAS guanyl releasing protein 1 (calcium and DAG-regulated) 001003 Thrombopathia
VPS13B Vacuolar protein sorting 13 homolog B (yeast) 001428 Trapped Neutrophil Syndrome
PLP1 Proteolipid protein 1 000770 Tremor, X-linked
VDR Vitamin D (1,25- dihydroxyvitamin D3) receptor 001431 Vitamin D-deficiency rickets, type II
VWF Von Willebrand factor 001057 Von Willebrand disease I
VWF Von Willebrand factor 001339 Von Willebrand disease II
VWF Von Willebrand factor 001058 Von Willebrand disease III
VWF Von Willebrand factor 001058 Von Willebrand disease III
IL2RG Interleukin 2 receptor, gamma 000899 Severe combined immunodeficiency disease, X-linked
Breed

Any

Extra diseases
Extra diseases

 

1, 2, 3


* If you are interested in analyzing any other disease, request that we add it to the panel.

Contact us and we will explain how we can help you

Functional panels, we group breeds phylogenetically, optimizing costs to offer you only what you need at a single price.

Our goal is to offer personalized genomic services adapted to the needs of both veterinarians and breeders as well as the families of furry animals. By optimizing the service we can offer reduced prices

Customer Testimonials

“I have worked with this laboratory on several occasions and I am very happy with them and their results. Their service is fast and efficient, and their prices are very competitive.”

Dolores Jiménez

Vet

“Omica is an excellent option for any veterinarian looking for accurate and reliable results. Their technicians are experts in their field and are always willing to help you with whatever you need.”

José Martínez

Vet

“They are very kind and attentive, helping us with everything we need and providing us with quality service. 100% recommended for any veterinarian who needs it.”

Javier Carreño

Vet

How does it work?

Painless and Simple. Personalize your patients’ care from a simple blood or saliva sample.

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