

Genomics transforms livestock breeding globally, boosting productivity and sustainability. In the U.S., SNP arrays guide dairy cattle selection since 2007. Europe targets milk yield and disease resistance. India’s NDDB and GenomeIndia advance genomic selection for local breeds. Standardized SNP arrays enhance diverse breed applications.
Our advanced lab supports global research organizations with cutting-edge genomics services.











Our animal genomics services leverage advanced sequencing to decode the genetic makeup of livestock, aqua and even wild animals, enhancing breeding, health, and sustainability. By identifying key genetic markers, we enable marker-assisted selection for traits like disease resistance, productivity, and environmental adaptability.
Utilizing next-generation sequencing and SNP microarrays, we deliver precise, actionable insights for optimized breeding programs. Our solutions empower breeders, animal research, and animal products organizations with data-driven decisions to improve herd quality and agricultural efficiency.
Genomics adoption in animal genetics is transforming livestock breeding worldwide, with widespread integration in North America, Europe, and Asia to enhance productivity and sustainability. In the U.S., genomic selection, introduced in 2007, is standard for dairy cattle, leveraging SNP arrays for precise trait selection. Europe’s dairy and beef industries use genomics for traits like milk yield and disease resistance, driven by cost-effective genotyping.
In India, the National Dairy Development Board’s programs and the GenomeIndia Project’s livestock initiatives are advancing genomic selection in breeds like Gyr and Sahiwal. Projects like the Bovine Pangenome Consortium globally and India’s Buffalo Genome Project promote standardized SNP arrays, accelerating adoption by providing accessible genetic tools for diverse breeds.






















Genetic testing is a process of testing genes and DNA to identify mutations or defects in the genes. These mutations can cause more than 3000 genetic disorders.
A genetic test is the ultimate diagnostic test. Once the disease-causing mutation is identified, prenatal diagnosis can be offered for all family members at risk to prevent genetic disorders. Some genetic tests identify a predisposition to cancer or other late-onset diseases so that preventive measures can be taken.
Genetic tests are either screening or diagnostic. Genetic screening tests will test if there is an elevated risk of a genetic disorder whereas diagnostic tests identify the defect with >99% accuracy. Genetic disorders can be identified at the chromosomal level or DNA level depending on the size of the defect involved. Cytogenetics (Karyotyping) is the study of chromosomes and Molecular genetics (Mutation analysis) is the study of DNA.
Not all genetic disorders are hereditary. Genetic disorders occurring in Somatic cells (cells other than Sperm or egg cells) are not hereditary. These genetic mutations are random events and cannot be passed to the next generation.