75 breakthrough innovations in one powerful instrument.
Science moves fast, and so do you. Access applications like single-cell, whole exome, and RNA sequencing, preparing for the future today.
Easier than ever. Accelerated decision making.
Experience our simplest workflow yet with dry instrumentation, easier run set up and DRAGEN on-board for 6x faster secondary analysis. Now with lossless genomic compression, saving up to 80% on storage costs.
See the system in your lab
Frame the QR code with your smartphone for a virtual view of the system on-location in your lab environment.
Simulate the system on-location in your lab environment.
Begin Virtual ViewSequencing power for the applications you need
NextSeq 2000 is redesigned from the ground up to maximize future proofing, offering sequencing power for high throughput applications. Offering scalability for evolving needs and larger studies, it supports a vast variety of applications, including:
Single-Cell Gene Expression
(100 cycles) 4k cells; 10k-50k reads/cell*
Examine the transcriptomes of individual cells for a high-resolution view of cell-to-cell variation. Explore the distinct biology of individual cells in complex tissues and understand cellular subpopulation responses to environmental cues. With P2 reagents, analyze 2-10 samples in approximately 13 hours. Or step up to P3 reagents to analyze 6-30 samples in approximately 19 hours.
*Recommended sequencing depth will largely depend on sample type and experimental objective and will need to be optimized for each study.
亚博官网人口Whole-Exome Sequencing
(200 cycles) 50× mean target coverage
Exome sequencing is a cost-effective approach when whole-genome sequencing is not practical or necessary. Efficiently identify coding variants across a broad range of applications, including population genetics, genetic disease, and cancer studies. In about 19 hours you can analyze 4 samples with P1 reagents. Or scale up to 16 samples in approximately 21 hours with P2 reagents, or 48 samples in approximately 33 hours with P3 reagents.
亚博官网人口Shotgun Metagenomics
(300 cycles) 50M reads/sample
Comprehensively sample all genes in all organisms present in a given complex sample. Evaluate bacterial diversity and detect the abundance of microbes in various environments or study unculturable microorganisms that are otherwise difficult or impossible to analyze. You can analyze 2 samples in about 19 hours with P1 reagents or step up to 8 samples in about 29 hours with P2 reagents. Scale up to 24 samples in approximately 48 hours with P3 reagents.
亚博官网人口Expand Your Access to More Data and Applications
High-Throughput Sequencing
Probe deeper into a single sample for insights or process more samples to improve statistical signficance.
Multiomics
Perform transformative science with access to multiple emerging high-throughput omics applications.
Efficient and Cost-Effective
Researchers talk about their experience using the NextSeq 1000 and NextSeq 2000 Sequencing Systems.
View Video
A simple, intuitive workflow to maximize your time and resources
The NextSeq 1000 and NextSeq 2000 Systems support emerging and mid-throughput sequencing applications as well as a broad range of methods such as exome sequencing, target enrichment, single-cell profiling, transcriptome sequencing, and more. They offer an intuitive workflow with load-and-go ease and visual cues about run status.
Prep
Support for a broad range of conventional and emerging applications
Sequence
Access mid-throughput sequencing
Analyze
Rapid, accurate, on-cloud or on-board data analysis
System Specifications
30-360 Gb*
output range100 M-2.4 B**
reads per run2 x 150 bp
max read length*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.
-
Interested in staying updated and informed on the release of the NextSeq 1000 and NextSeq 2000 Systems?
Sign up now.
Sign up now.