We offer platforms from gold standard sanger sequencing to simple and scalable next-generation sequencing (NGS) to meet your needs. Our sequencing platforms use optimized applications, high-quality consumables, and integrated analysis solutions to achieve fast, accurate, and affordable results.
Sanger sequencing is used to study a small subset of genes linked to a defined phenotype, confirm next-generation sequencing (NGS) variants, detect minor allele fractions down to 5%, or read contiguous sequences up to 1,000 bases.
NGS technologies are able to analyze millions to billions of DNA sequences in parallel with high sensitivity. With its cost dropping at a consistent rate over the last decade, NGS becomes increasingly popular in a broad range of applications, including gene expression profiling, chromosome counting, detection of epigenetic changes, and molecular analysis. NGS is driving the exciting future of personalized medicine.
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