The P2 kitted reagents include dual-indexing support on a P2 flow cell with up to 400M reads for small whole-genome sequencing, whole-exome sequencing, and single cell RNA sequencing.View Products
A fast, integrated workflow for a wide range of applications providing targeted resequencing for custom panels, fixed panels, and whole-exome enrichment.
Data management and simplified bioinformatics for labs getting started and for rapidly scaling next-generation sequencing (NGS) operations.
iCredits are the currency used to purchase Illumina genomic data storage and analysis options.
This kit combines next-generation sequencing with epigenetic insights to accelerate biomarker discovery and understand methylation’s role in gene regulation.
Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and formalin-fixed, paraffin-embedded (FFPE) tissue.
Simple, cost-effective chromatin immunoprecipitation sequencing (ChIP-Seq) DNA library preparation, with master mixes and robust multiplex capabilities.
The Illumina DRAGEN (Dynamic Read Analysis for GENomics) Bio-IT Platform provides accurate, ultra-rapid secondary analysis of sequencing data, addressing common challenges surrounding compute times and massive volumes of data.View Products
BaseSpace Sequence Hub offers NGS data analysis apps for common Illumina sequencing methods.
These tools accelerate coronavirus detection and identification, simplify sample tracking, and help scientists contribute to public databases, free of charge.
BaseSpace Variant Interpreter allows scientists to rapidly identify biologically significant variants from human genomic 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.
DesignStudio is a web-based assay design tool to help researchers design and order custom sequencing probes, or create custom genotyping array assays.
Phosphorus uses the DRAGEN Bio-IT Platform to perform genomics data analysis onsite and at an accessible price point.Read Interview
Access a full suite of services designed to maximize performance and productivity. From instrument service plans and training to qualification services and free instrument performance services – we are here to support all of your customer needs.Learn More
This central hub offers education and assistance for your workflow, from start to finish. Learn about our technology, design your project, access selection tools, find software to glean valuable insights from your data, then purchase what you need and get support.Learn More