The NextSeq Series delivers the power of high-throughput sequencing with the speed, simplicity, and affordability of a benchtop next-generation sequencing (NGS) system. The NextSeq 500 and NextSeq 550 Systems fit seamlessly into research laboratories, without need for specialized equipment. Perform many combinations of high- and mid-throughput sequencing applications to advance your studies.
NextSeq systems are efficient and flexible to handle a range of different types of projects. Perform whole-genome, transcriptome, and targeted resequencing applications with a rapid, one-day turnaround. Easily switch between two flow cell configurations to tune your output based on your current research needs for applications or sample batch sizes.
Designed to reduce setup time, the NextSeq Series features a load-and-go workflow and an intuitive user interface. Simply load flow cells and reagent cartridges and then sequence at the touch of a button. The NextSeq Series integrates cluster generation, sequencing by synthesis, and base calling into a single system. Researchers can review real-time data and performance metrics from anywhere at any time.
To streamline run management, downstream analysis, and data sharing, the NextSeq Series is integrated with BaseSpace Sequence Hub. This Illumina informatics solution, available in both cloud and on-site packages, enables researchers to go from sample to results without bioinformatics expertise.
Learn how this lab is leveraging the power of Illumina next-generation sequencing for their cutting-edge work in virology.View Video
Whole-genome sequencing with the MiSeq and NextSeq Systems enables researchers to examine nucleosome patterns and infer the gene expression status of cancer drive genes.Read Article
Ease of use and high-quality data supported a smooth transition from CGH microarrays to the Infinium CytoSNP-850K BeadChip.Read Article
These sequencing reagent kits offer a simplified workflow and improved data quality compared to the prior v1 kit version.
Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.