Ready-to-use, cartridge-based reagents combined with multiple flow cell configurations create a combination of scalable throughput and flexibility for virtually any genome, sequencing method, and scale.Learn More
Simple, all-inclusive whole-genome sequencing (WGS) library preparation that provides accurate and comprehensive coverage of complex genomes.
A robust, highly scalable whole-transcriptome analysis (RNA-Seq) solution for a variety of species and sample types, including human, mouse, and formalin-fixed, paraffin-embedded (FFPE) tissue.
This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.
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
BaseSpace Sequence Hub provides a user-friendly, scalable, and secure cloud-computing platform for storage and analysis of genomic data. Monitor sequencing runs remotely, and share data easily with collaborators. Our rich ecosystem of BaseSpace Apps makes data analysis simple and accessible for a wide range of sequencing applications.Learn More
Combines per-cycle BCL files from a run and translates them into demultiplexed FASTQ files for downstream data analysis.
Setting up and running sequencing experiments is easy with software tools designed for Illumina sequencing systems.
BaseSpace Clarity LIMS is a laboratory information management system that helps laboratories track samples and optimize procedures and workflows.
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 NovaSeq 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.