HiSeq 3000/4000 SBS Kits leverage patterned flow cell technology for even cluster spacing and uniform feature size, delivering extremely high cluster densities and significant increases in data output and daily throughput.Learn More
This kit enables cluster generation for subsequent sequencing on the HiSeq 3000 and HiSeq 4000 Systems.
Provides reagents for Single Read (SR) cluster generation on the cBot2 System. Cluster reagents are compatible with the HiSeq 3000 and HiSeq 4000 Systems.
This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.
This exome sequencing library prep kit uses a simple, one-day workflow to provide a fast path to greater understanding of the human exome.
This kit combines next-generation sequencing with epigenetic insights to accelerate biomarker discovery and understand methylation’s role in gene regulation.
The cBot 2 System streamlines the sequencing workflow by automating cluster generation. It is a required accessory instrument for HiSeq sequencers.
Illumina offers high throughput-compatible library prep kits and partnerships with leading automation vendors.
Our laboratory information management system helps researchers track samples and optimize procedures and workflows.
User-friendly touchscreen–operated instrument control software guides users through each step of the sequencing workflow, from experiment setup to reagent and flow cell loading. The software also generates real-time quality statistics for accurate run monitoring.View Software
DesignStudio is a web-based assay design tool to help researchers design and order custom sequencing probes, or create custom genotyping array assays.
Setting up and running sequencing experiments is easy with software tools designed for Illumina sequencing systems.
Simplify your bioinformatics with an economical and powerful computing environment to manage, analyze, and share data.
BaseSpace Correlation Engine mines over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research.
BaseSpace Cohort Analyzer allows you to integrate and analyze subject and genomic data together using innovative visualization and analysis tools.
BaseSpace Variant Interpreter enables genetic labs to rapidly identify biologically significant variants from human genomic data.
Illumina services and support begins when the HiSeq System 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, hands-on courses and web-based training options.
Illumina provides services that connect an experienced team direct to the laboratory to jump-start successful sequencing workflow implementation.