Explore sequencing and microarray products to advance breakthroughs in rare and genetic diseases.
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A high-performance, fast, and reliable human whole-exome sequencing solution that includes a comprehensive, up-to-date exome enrichment panel.
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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 WGS provides an unbiased view of the entire human genome and the genetic variants that encode human traits and disease.