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As scientists obtain and analyze genomic sequence information, more genetic variants are identified. As the field moves toward trying to understand the significance and potential utility of these variants, the need for rapid, reliable methods of detection has emerged.
Thermo Fisher Scientific offers real-time PCR products and other tools specifically designed for genotyping and genetic variation research, covering the entire process from isolating and purifying genomic DNA, selecting probes and primers, and DNA amplification, to performing allelic discrimination and data analysis.
Over 17 million predesigned assays for SNP genotyping and drug metabolism enzyme (DME).
Explore: SNP genotyping
Facilitate high sample throughput for mid-density genotyping.
Explore:SNP genotyping OpenArray
Allows specific, reproducible, and easy-to-interpret copy number results.
Explore:Copy number variation
Detect and quantitate very small amounts of mutant DNA in a background of wild type DNA using competitive allele-specific PCR (castPCR).
Explore: Rare mutation detection
Detect polymorphisms in high-value DME pharmacogenetics markers, including PharmaADME core markers.
Explore: DME profiling
Identify variations in nucleic acid sequences by detecting small differences in PCR melting (dissociation) curves.
Explore: High resolution melt analysis
For Research Use Only. Not for use in diagnostic procedures.