Epigenetic breakthroughs with the Illumina NextSeq 1000/2000
Learn about innovations of the NextSeq 1000/2000 workflow, including the use of 3D genomics to study the functional context of GWAS variants in this webinar.
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Proven technology to power your discovery
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The NextSeq 1000 and NextSeq 2000 Systems are thoughtfully designed to enable more insights on your benchtop. With 14 configurations and read lengths from 1 × 50bp to 2 × 300bp, these systems efficiently handle benchtop workflows while driving down costs and minimizing waste. Confidently expand your research 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, more economical, and higher quality sequencing than ever before.
The NextSeq 1000 and NextSeq 2000 Systems offer the certainty of a field-tested solution and a reliable sequencing partner. Take advantage of a large ecosystem of applications, protocols, and informatics built in collaboration with thousands of researchers and thought leaders across the globe.
Access a wide range of applications including single-cell, whole-exome, and RNA sequencing—all on the market-leading benchtop platform.
Expand your capabilities. Achieve 1.8 billion single-end reads per run to power the most data intensive applications on your benchtop sequencer.
System specifications
a. Specifications based on Illumina PhiX control library at supported cluster densities.
The NextSeq 1000 and NextSeq 2000 Systems provide a comprehensive workflow that includes user-friendly run setup, a wide ecosystem of compatible library prep kits, load-and-go operation, and integrated, onboard secondary analysis.
Track samples and manage runs easily and efficiently with cloud-based and on-premises options.
Prepare libraries with a wide range of compatible library preparation kits.
Generate sequences with scalable output, efficient run times, and high data quality.
Analyze using onboard DRAGEN secondary analysis or stream to the cloud for additional analysis flexibility.
Access BaseSpace apps, instrument performance data, license management, and long-term storage solutions.
When you partner with Illumina, you’ll get more than just leading-edge technology–you become part of a community with like-minded goals.
Learn about innovations of the NextSeq 1000/2000 workflow, including the use of 3D genomics to study the functional context of GWAS variants in this webinar.
Perform transformative science with access to multiple emerging omics applications.
NextSeq 1000 and NextSeq 2000 Systems |
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Maximum output per runa,b | 15 Gb | 120 Gb | 540 Gbc | 8 Tb |
Maximum single reads per runb | 25M | 400M | 1.8Bc | 26B |
Maximum read length | 2 × 300 bp | 2 × 150 bp | 2 × 300 bp | 2 × 150 bp |
Informatics optionsd | On-premises All DRAGEN Pipelines Cloud DRAGEN Pipelines available on BSSH and ICA |
On-premises All DRAGEN Pipelines Cloud DRAGEN Pipelines available on BSSH and ICA |
On-instrument Popular DRAGEN Pipelines available onboard On-premises All DRAGEN Pipelines Cloud DRAGEN Pipelines available on BSSH and ICA |
On-instrument Popular DRAGEN Pipelines available onboard On-premises All DRAGEN Pipelines Cloud DRAGEN Pipelines available on BSSH and ICA |
a. Based on Illumina PhiX control library at supported cluster densities.
b. Data is based on single flow cell output. The NovaSeq X Plus System is capable of single flow cell runs or dual flow cell runs. The NovaSeq X System is capable of single flow cell runs.
c. Specifications are based on a P4 flow cell run. P4 flow cells are available for the NextSeq 2000 System only.
d. View key DRAGEN applications for more details.
Interested in learning more about the flexibility of NextSeq 1000 and NextSeq 2000 Systems? Contact us today to answer your questions.
Your email address is never shared with third parties.