Science moves fast, and so do you. Access applications ranging from targeted sequencing to data-rich multiomics applications including whole-exome, spatial transcriptomics, and single-cell sequencing. Scalability to help you prepare for the future today.
Experience our simplest workflow yet with easier run setup, time-saving dry instrumentation, and DRAGEN on-board for no additional cost, providing accurate and efficient secondary analysis, up to 6x faster. Now with lossless genomic compression, saving up to 80% on storage costs.
Frame the QR code with your smartphone for a virtual view of the system on-location in your lab environment.
The NextSeq 1000 and NextSeq 2000 are redesigned from the ground up. Their flexibility, affordability, and scalability help both new and experienced users achieve fast turnaround times and reduced operating costs. With the wide range of available flow cells, they support a variety of applications including:
Examine the transcriptomes of individual cells for a high-resolution view of cell-to-cell variation.
Efficiently identify coding variants across a broad range of applications, including population genetics, genetic disease, and cancer studies.
Comprehensively sample all genes in all organisms present in a given complex sample.
Pinpoint predictive cellular state and their spatial localization to understand the influence of the cellular and spatial architecture on the microenvironment.
Analyze both coding RNA and multiple forms of noncoding RNA for a comprehensive view of the transcriptome.
Infectious Disease Research Description: A universal, culture-free method for infectious disease characterization and surveillance that may be used with viruses, bacteria, fungi, and parasites, and can replace the need for multiple tests.
High-intensity sequencing applications generate dramatically more data for more impactful insights.
Perform transformative science with access to multiple emerging high-throughput omics applications.
The NextSeq 1000 and NextSeq 2000 Systems support a wide range of methods such as exome sequencing, target enrichment, single-cell profiling, transcriptome sequencing, and more. With DRAGEN onboard, the systems offer an intuitive workflow with load-and-go ease and push-button bioinformatics analysis.
Support for a broad range of conventional and emerging applications
Access best-in-class benchtop sequencing accuracy, performance, and throughput
Rapid, accurate analysis in the cloud and on-instrument
*Specifications based on Illumina PhiX control library at supported cluster densities.
**100 M - 1.2 B single reads per run. 200 M - 2.4 B paired-end reads per run.
When you partner with Illumina, you’ll get more than just leading-edge technology–you become part of a community with like-minded goals.