Illumina NextSeq 2000 Sequencing System

Illumina NextSeq 2000 Sequencing System

Illumina NextSeq 2000 Sequencing System

Brief Description
The Illumina NextSeq 2000 is an advanced next-generation sequencing (NGS) platform designed for rapid, flexible, and high-quality genomic analysis. Using Illumina’s Sequencing by Synthesis (SBS) technology, the system can generate hundreds of millions to over one billion sequencing reads per run with exceptional accuracy. It supports a broad range of applications, including whole-genome sequencing (WGS), RNA sequencing (RNA-Seq), metagenomics, targeted sequencing, and single-cell genomics. Multiple flow cell configurations allow data output to be tailored to the requirements of individual projects, making the NextSeq 2000 an ideal solution for medium- to high-throughput sequencing.

Specifications

Platform Overview

The NextSeq 2000 is a high-throughput sequencing platform designed for large-scale genomic and transcriptomic studies while maintaining the compact footprint of a benchtop instrument. It is based on the NextSeq 1000 architecture but supports higher-capacity P3 and P4 flow cells, enabling substantially increased data output.

Using XLEAP-SBS chemistry, the system can generate up to 540 Gb of sequencing data per run, depending on the selected flow cell and read configuration.

Sequencing Performance

  • Data output: Up to 540 Gb per run
  • Read lengths: Up to 2 × 300 bp
  • Quality scores: Typically >90% of bases ≥ Q30 for read lengths up to 150 bp

Integrated Computing

  • 2U microserver
  • 288 GB RAM
  • 3.8 TB SSD storage
  • Linux CentOS operating system
  • Integrated DRAGEN FPGA-accelerated secondary analysis for rapid onboard processing

Optical System

  • Three laser sources:
    • 449 nm
    • 523 nm
    • 820 nm
  • Class 1 laser device

Physical Specifications

  • Dimensions: 55 × 65 × 60 cm
  • Weight: Approximately 141 kg

Supported Applications

  • Whole-genome sequencing (WGS)
  • Whole-exome sequencing (WES)
  • Large-scale RNA-Seq studies
  • Single-cell RNA sequencing
  • Comprehensive tumor genomic profiling
  • Large-scale microbiome studies

The combination of high throughput and integrated bioinformatics makes the NextSeq 2000 particularly well suited for large genomic studies, clinical genomics, and population-scale sequencing projects.

Additional information

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Operating rules

Fees

Sample preparation

Consumables

Applications (clinical protocols, basic research)

Publications

Funding

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