Human Genomics
The Path Forward for Human Genetics
Neogen® Genomics’ capabilities include a variety of technology platforms from individual SNP genotyping to whole genome sequencing. Combined with cutting edge technology and innovation, our sophisticated genetic analytics and ISO and CLIA certification allows researchers and businesses to consider what can be possible for genetic testing in humans.
CLIA Certified Labs to Make a World of Difference
Genomics in Healthcare
- Disease Analysis
- Drug Presence
- Genetic Traits & Disease Inheritance
- Genetic & Rare Diseases
- Immunology
- Pharmacogenomics
- Reproductive Health
Genomics in Research
- Cancer Research
- Neuroscience
Expand Your Customer Base with Comprehensive Genomic Testing
Custom Genotyping
A broad range of custom genotyping options for projects that may be focused on specific regions of interest or enhancing areas of coverages on a current array product and custom sequencing.
Infinium™ MethylationEPIC BeadChip
Robust methylation profiling microarray with extensive coverage of CpG islands, genes, and enhancers. Use for epigenome-wide association studies.
Infinium™ Global Screening Array (GSA) v3.0 BeadChip
A powerful, high-quality, cost-effective array for population-scale genetic studies. The Infinium Global Screening v3.0 BeadChip builds on the success of its consortium version that has been widely adopted human disease researchers, health care networks, and consumer genomics companies.
Axiom Precision Medicine Diversity Array
The Axiom Precision Medicine Diversity Research Array (PMDA) is a comprehensive genotyping array containing more than 850,000 variants relevant to human focused research, genetic testing, and more.
Human Whole-Genome Sequencing (WGS)
Accessing and Analysis of the Human Genome has never been easier. Human WGS can evaluate every base in the genome and navigate the complexity of genomic variants that make us unique.
U.K. Biobank Axiom Array
The U.K. Axiom Biobank Genotyping Array can be used to genotype a large number of genetic variants in a single assay. This array is of genotyping nearly 1 million genetic variants, SNPs, copy number variants (CNVs), and indels.