Next-generation sequencing (NGS) is driving new and exciting discoveries across applications, from single cell analysis, liquid biopsy research, circulating-free DNA (cfDNA) studies, genome wide association studies, metagenomics and targeted sequencing. Our innovative and high-quality NGS panels and kits can alleviate workflow challenges and help reveal meaningful insights from your results.
We employ a digital sequencing approach using molecular barcodes to overcome issues associated with PCR duplicates such as false positives and library bias. So, whether you’re looking to analyze copy number variation (CNV) or detect SNPs, InDels or other mutations and allelic differences, we have a DNA-seq solution that lets you detect your low-frequency variants of interest with confidence.