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.

詳細を確認

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

FFPE 組織やその他の品質の低いサンプルからのRNAのシーケンスに適した再現性の高い経済的なソリューションです。わずか10 ng の total RNA から精確なデータを得ることができます。

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

少量のDNAインプットで、小さなゲノム、PCRアンプリコン、およびプラスミドのシーケンスライブラリーを90分以内で調製できます。


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.

Learn More
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.

Learn More

Illumina DRAGEN Bio-IT Platform

イルミナのDRAGEN (Dynamic Read Analysis for GENomics) Bio-IT Platformは、精確で超高速なシーケンスデータの二次解析を実現します。

DesignStudioカスタムアッセイデザインツール

DesignStudio is a web-based assay design tool to help researchers design and order custom sequencing probes, or create custom genotyping array assays.

BlueFuse Multiソフトウェア

BlueFuseソフトウェアは分子細胞遺伝学およびIVFにおけるデータ解析を1つのフレームワークで実施します

BaseSpace Cohort Analyzer

BaseSpace Cohort Analyzerでは、革新的な可視化ツールと解析ツールを用いて対象データとゲノムデータを統合し、一緒に解析することができます。

BaseSpace Correlation Engine

BaseSpace Correlation Engineは、20,000を超えるゲノム研究から遺伝子、実験、薬剤、および表現型に関するデータに基づく答えを引き出し、お客様の研究をサポートします。

BaseSpace Variant Interpreter

BaseSpace Variant Interpreterにより、ゲノムラボではヒトゲノムデータから生物学的に重要なバリアントを迅速に同定することができます。


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

Read Interview
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.