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.
Interactive omics knowledge base that puts private omics data in biological context with highly curated public data.