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。
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.
Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA.
This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.
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.
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 MoreSimplify your bioinformatics with an economical and powerful computing environment to manage, analyze, and share data.
Learn MoreIllumina DRAGEN (Dynamic Read Analysis for GENomics) Bio-IT Platform provides accurate, comprehensive, and efficient analysis of next generation sequencing data.
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 allows you to integrate and analyze subject and genomic data together using innovative visualization and analysis tools.
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 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
Read InterviewIllumina 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.
In addition to the 1-year basic service warranty included with system purchase, Illumina offers maintenance, repair, and qualification solutions.
Get high-quality results on Illumina technology even faster with instructor-led or hands-on courses and web-based training options.
Bring an experienced Illumina team to your lab to jump-start successful sequencing workflow implementation.
Verify instrument installation, operation, or performance and obtain an audit-ready report to help meet regulatory requirements.
Connect to Illumina Proactive to access this complimentary instrument performance monitoring and proactive support service.