Sequencing and microarray kits and reagents help translational and clinical researchers investigate the role of genetic variation in cancer, rare diseases, reproductive health, and more.
Our clinical cancer research solutions deliver accurate genomic information, and enable labs to analyze multiple genes in a single test.
NGS technology is helping to drive breakthroughs in genetic disease testing by facilitating early detection and diagnosis.
As a hypothesis-free method, NGS can distinguish between infectious disease strains that differ by as little as one SNP, and replace multiple tests.
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