Products to support speed and simplicity for everyday genomics

Featured products and software solutions for the NextSeq 550 System

NextSeq Products and Services

NextSeq 500/550 v2.5 Reagent Kits
NextSeq 500/550 v2.5 Reagent Kits

Bring the power of a high-throughput sequencing system to the benchtop. Flexible configurations support a range of applications from whole-genome sequencing and large targeted resequencing panels to gene expression profiling and other counting applications.


TruSight Oncology 500
TruSight Oncology 500

Tumor mutational burden (TMB)、マイクロサテライト不安定性(MSI)などを含むさまざまなバリアントタイプをターゲットとしたアッセイです。

TruSeq Stranded mRNA
TruSeq Stranded mRNA

Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.

TruSeq DNA Nano
TruSeq DNA Nano

Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA.

TruSeq DNA Exome
TruSeq DNA Exome

This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.

TruSeq RNA Exome
TruSeq RNA Exome

Provides a reproducible, economical solution for sequencing RNA from FFPE tissues and other low-quality samples. Accuracy from as little as 10 ng total RNA.

Nextera XT DNA Library Preparation Kit
Nextera XT DNA Library Preparation Kit


Automating sequencing library preparation improves consistency, reduces hands-on time, and enables higher throughput. Access Illumina-qualified methods for automated library prep available through our partnerships with leading vendors.

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High-Throughput Library Prep Automation
BaseSpace Sequence Hub
BaseSpace Sequence Hub

Simplify your bioinformatics with an economical and powerful computing environment to manage, analyze, and share data.

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Illumina DRAGEN Bio-IT Platform

Illumina DRAGEN (Dynamic Read Analysis for GENomics) Bio-IT Platform provides accurate, comprehensive, and efficient analysis of next generation sequencing data.



BlueFuse Multiソフトウェア


BaseSpace Cohort Analyzer

BaseSpace Cohort Analyzer allows you to integrate and analyze subject and genomic data together using innovative visualization and analysis tools.

BaseSpace Correlation Engine

BaseSpace Correlation Engine mines over 23,000 (and growing) scientific studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research.

BaseSpace Variant Interpreter

BaseSpace Variant Interpreter allows scientists to rapidly identify biologically significant variants from human genomic data.

See how Phosphorus uses the DRAGEN™ Bio-IT Platform to perform genomics data analysis

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Bring Bioinformatics In-House to Cut Costs and Time
Comprehensive Scientific Support

Illumina services and support begins when the NextSeq Series is delivered. Illumina scientists and engineers assist with NGS system installation and setup and train laboratory personnel. In addition to onsite support, training courses are available to bring laboratory personnel quickly up to speed.

Illumina scientists are available 24/7 globally to answer questions every step of the way, enabling researchers to focus on making the next breakthrough discovery.

Illumina Product Support Services

In addition to the 1-year basic service warranty included with system purchase, Illumina offers maintenance, repair, and qualification solutions.

Illumina University Training

Get high-quality results on Illumina technology even faster with instructor-led or hands-on courses and web-based training options.

Illumina Consulting Services

Bring an experienced Illumina team to your lab to jump-start successful sequencing workflow implementation.

Instrument Qualification Services

Verify instrument installation, operation, or performance and obtain an audit-ready report to help meet regulatory requirements.

Proactive Instrument Monitoring

Connect to Illumina Proactive to access this complimentary instrument performance monitoring and proactive support service.