HiSeq Rapid v2 SBS Kits enable the longest reads on HiSeq instruments, with reads up to 2x250 bp. The new kits generate up to 300 Gb of data per run. HiSeq Rapid SBS Kits v2 are the ideal choice for sequencing on HiSeq systems.Learn More
Reagents for determining the DNA sequence of each cluster on a flow cell using sequencing by synthesis technology on enabled HiSeq systems.
This kit uses isothermal amplification to create clonal clusters of ~1000 copies each, ready for sequencing on enabled HiSeq systems.
These kits contain ready-to-load reagents to determine the DNA sequence of each cluster on a HiSeq flow cell using sequencing by synthesis technology.
The cBot 2 System streamlines the sequencing workflow by automating cluster generation. It is a required accessory instrument for HiSeq sequencers.
This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.
Simple, all-inclusive whole-genome sequencing (WGS) library preparation that provides accurate and comprehensive coverage of complex genomes.
User-friendly touchscreen–operated instrument control software guides users through each step of the sequencingworkflow, from experiment setup to reagent and flow cell loading. The software also generates real-time quality statisticsfor accurate run monitoring.Learn More
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 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, hands-on courses and web-based training options.
Illumina provides consulting services that connect an experienced Illumina team direct to the laboratory to jump-start successful sequencing workflow implementation.