Explore sequencing and microarray products to advance breakthroughs in rare and genetic diseases.
Featured products
A high-performance, fast, and reliable human whole-exome sequencing solution that includes a comprehensive, up-to-date exome enrichment panel.
View productFeatured products
Genotyping array providing a scalable, cost-effective solution for population genetics, pharmacogenomics studies, and precision medicine research.
View productNGS technology is helping to drive breakthroughs in genetic disease testing by facilitating early detection and diagnosis.
Rare disease whole-genome sequencing
Whole-genome sequencing is the most comprehensive test for rare disease, with the potential for superior diagnostics and outcomes.
Human whole-genome sequencing provides the most detailed view into the complex genetic variants that make us unique.