Kits, related products, and software solutions
Speed and simplicity for everyday genomics
Ready-to-use reagent kits deliver the power of high-throughput sequencing 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.
NextSeq 500/550 v2.5 sequencing reagent kits deliver the power of high-throughput sequencing on a benchtop system with increased stability and robustness.
NextSeq 500/550 v2.5 sequencing reagent kits deliver the power of high-throughput sequencing on a benchtop system with increased stability and robustness.
NextSeq 500/550 v2.5 sequencing reagent kits deliver the power of high-throughput sequencing on a benchtop system with increased stability and robustness.
Illumina DNA Prep offers flexibility for many whole-genome sequencing applications.
PhiX Control v3 is a reliable, adapter-ligated library used as a control for Illumina sequencing runs. The library is derived from the small, well-characterized PhiX genome, offering several benefits for sequencing and alignment.
Illumina Total RNA Prep with Ribo-Zero Plus provides exceptional performance for the analysis of coding and multiple forms of noncoding RNA. Gain high-confidence discovery of alternative transcripts, gene fusions, and allele-specific expression.
High-throughput library prep automation
To aid with adopting automation, methods for many of our library prep assays are available from the leading automation companies. Our partners offer a range of automation platforms to address your lab's throughput needs.
Laboratory information management systems (LIMS)
By using a LIMS, your lab can automate workflows, track reagents and lots, integrate instruments, and manage samples and associated information.
Manage, analyze, and share NextSeq 550 System data using BaseSpace Sequence Hub, a cloud computing data management platform that supports Illumina DRAGEN Secondary Analysis.
Accurate, comprehensive, and efficient secondary analysis of next-generation sequencing (NGS) data.
BlueFuse software provides molecular cytogenetic and in vitro fertilization (IVF) data analysis in a single framework.
Interactive omics knowledge base that puts private omics data in biological context with highly curated public data.
Our variant annotation and analysis software tools can help researchers extract and report biological insights from large volumes of genomic data.
This remote instrument performance monitoring service helps you minimize unscheduled downtime for your Illumina sequencers.
Qualify Illumina laboratory instruments with professional services direct from the manufacturer.
Access a full suite of accurate, expedient solutions ranging from instrument service plans to qualification services and training.
Get hands-on NGS and microarray training from expert instructors. We also offer live or self-paced online courses and other educational resources.