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Optimal Selection™ Feline + DNA Profile with Parentage Service


Streamline your genetic testing with an all-in-one Optimal Selection™ Feline bundle. With one simple cheek swab, you'll get Optimal Selection™ Feline and an ISAG 2020 DNA profile, with complimentary self-service parentage testing for user accounts with multiple Wisdom provided ISAG 2020 DNA profiles.


Product bundle includes:

ISAG 2020 DNA Profile + Parentage Service - New!

Permanently identify your breeding cat's unique genetic "fingerprint" using ISAG 2020—the most advanced profiling panel—and confirm pedigree with parentage reporting.*

See a sample DNA report with parentage and profile certificates included

Benefits include:

  • Verify the sire of litters prior to registration
  • Eliminate pedigree uncertainties
  • Utilize for registration with cat fancier associations
  • Use for sperm banking and import/export with pre-established DNA profiles
  • Obtain certificates for parentage and DNA profiling

*Profiling and parentage do not determine breed or purebred status

Optimal Selection Feline testing panel

Our leading genetic testing panel for both pedigreed and mixed-breed cats includes 40+ genetic health tests, plus blood type, along with traits and genetic diversity.

Click to see a sample technical report
Click to see a sample dashboard

Our preferred testing panel for cat breeders, Optimal Selection Feline, is breed-focused and backed by science, for use on any pedigreed or mixed-breed cat to screen for health, traits, blood type, and genetic diversity.  We’ve taken the latest scientific research on cat population genetics and developed a simple and easy at–home swab test for the modern breeder to manage their cats' health and help reduce guesswork on litter colors and traits. Our genome-wide testing panel provides advantages over traditional techniques such as pedigree analysis, and helps breeders to develop proactive, sustainable breeding programs for themselves and their wider breed. It's no surprise that Optimal Selection Feline is used by breeders, veterinarians and researchers worldwide. The test includes:

  • Results for over 40 genetic diseases, with breed relevance noted in reports
  • Testing for 20+ traits including coat colors, coat types, and body shape
  • Comprehensive blood typing
  • Genetic diversity information
  • Continuously updated research and breed information based on new discoveries

Optimal Selection™ DNA service for cats is a genome-wide genetic analysis that gives information on several inherited characteristics. All received DNA test results are reported online to your user account in the secured Optimal Selection™ database.

Included Health Tests

  • Acute Intermittent Porphyria (Variant 1)
  • Acute Intermittent Porphyria (Variant 2)
  • Acute Intermittent Porphyria (Variant 3)
  • Acute Intermittent Porphyria (Variant 4)
  • Acute Intermittent Porphyria (Variant 5) - NEW!
  • Autoimmune Lymphoproliferative Syndrome
  • Blood Type
  • Burmese Head Defect
  • Chediak-Higashi Syndrome (Discovered in Persian cats) - NEW!
  • Congenital Adrenal Hyperplasia
  • Congenital Erythropoietic Porphyria
  • Congenital Myasthenic Syndrome
  • Cystinuria Type 1A
  • Cystinuria Type B (Variant 1)
  • Cystinuria Type B (Variant 2)
  • Cystinuria Type B (Variant 3)
  • Dihydropyrimidinase Deficiency
  • Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold)
  • Factor XII Deficiency (Variant 1)
  • Factor XII Deficiency (Variant 2) - NEW!
  • Familial Episodic Hypokalaemic Polymyopathy (Discovered in Burmese)
  • Glutaric Aciduria Type II - NEW!
  • Glycogen Storage Disease
  • GM1 Gangliosidosis
  • GM2 Gangliosidosis
  • GM2 Gangliosidosis, type II (Discovered in Burmese cats) - NEW!
  • GM2 Gangliosidosis, type II (Discovered in domestic shorthair cats)
  • GM2 Gangliosidosis, type II (Discovered in japanese domestic cats)
  • Hemophilia B (Variant 1)
  • Hemophilia B (Variant 2)
  • Hyperoxaluria type II
  • Hypertrophic Cardiomyopathy (Discovered in Maine Coon)
  • Hypertrophic Cardiomyopathy (Discovered in Ragdoll)
  • Hypotrichosis (Discovered in Sacred Birman)
  • Lipoprotein Lipase Deficiency
  • Mucopolysaccharidosis Type I
  • Mucopolysaccharidosis Type VI (G1558A variant) - NEW!
  • Mucopolysaccharidosis Type VI (T1427C variant)
  • Mucopolysaccharidosis Type VII
  • Mucopolysaccharidosis VII
  • Multidrug Resistance 1
  • Myotonia Congenita
  • Polycystic Kidney Disease (PKD)
  • Progressive Retinal Atrophy (rdAc-PRA)
  • Progressive Retinal Atrophy (Discovered in Bengal cats)
  • Progressive Retinal Atrophy (Discovered in Persian cats) - NEW!
  • Pyruvate Kinase Deficiency
  • Sphingomyelinosis (Variant 1)
  • Sphingomyelinosis (Variant 2)
  • Spinal Muscular Atrophy
  • Vitamin D-Dependent Rickets

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