注目製品
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.
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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
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.
TruSeq DNA Nano
Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA.
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
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
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。
High-Throughput Library Prep Automation
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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Software and Informatics Solutions
BaseSpace Sequence Hub
Simplify your bioinformatics with an economical and powerful computing environment to manage, analyze, and share data.
Learn MoreIllumina DRAGEN Bio-IT Platform
The Illumina DRAGEN (Dynamic Read Analysis for GENomics) Bio-IT Platform provides accurate, ultra-rapid secondary genomic analysis of sequencing data.
DesignStudioカスタムアッセイデザインツール
DesignStudioは、カスタムシーケンスプローブのデザインと注文、カスタムジェノタイピングアレイアッセイの作製に役立つウェブベースのアッセイデザインツールです。
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 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 20,000 genomic 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.
Bring Bioinformatics In-House to Cut Costs and Time
See how Phosphorus uses the DRAGEN™ Bio-IT Platform to perform genomics data analysis
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Instrument Services
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.