The NextSeq 1000 and NextSeq 2000 Systems are enabling biological insights with breakthrough innovative features thoughtfully designed in a compact, yet versatile platform. With up to 14 configurations and read lengths from 1x50bp to 2x300bp, these systems efficiently handle benchtop workflows with flexibility and scalability. Efficient design combined with intuitive workflows deliver ease of use while driving down costs and minimizing waste. Confidently expand your research with single-cell and spatial sequencing and other emerging applications with the NextSeq 1000 and NextSeq 2000 Systems.
These systems offer operational ease and onboard informatics, simplifying workflows for both new and advanced users. Advanced XLEAP-SBS chemistry, built on the proven foundation of standard Illumina SBS chemistry, enables faster and higher quality sequencing than ever before. Coupled with high-efficiency and low-cost workflows, the NextSeq 1000 and NextSeq 2000 Sequencing Systems deliver technological advancements for diverse sequencing applications.
The NextSeq 1000 and NextSeq 2000 Systems offer the certainty of a field-tested solution and a reliable sequencing partner. Joining this community gives access to a large ecosystem of applications, protocols, and informatics that have been built in collaboration with thousands of researchers and industry thought leaders across the globe.
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.
Researchers talk about their experience using the NextSeq 1000 and NextSeq 2000 Sequencing Systems.
View VideoThe 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.
When you partner with Illumina, you’ll get more than just leading-edge technology–you become part of a community with like-minded goals.
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