Illumina Genomics Products

Sequencing and microarray products for diverse applications


Nextera DNA Flex

A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbes.

TruSeq RNA Exome

An economical solution for sequencing RNA from FFPE tissues and other low-quality samples.

MiSeq Reagent Kits v3

Achieve up to 15 Gb of output with improved cluster density, read length, and quality scores.

NextSeq 500/550 v2.5 Kits

These reagents offer increased stability and robustness over the v2 kit version.

Find the system that's right for you and your lab. Explore the entire porfolio of Illumina sequencing systems and microarray scanners.

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Library Prep and Array Kit Selector

Determine the best kit for your needs based on your project type, starting material, and method of interest.

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Sequencing Platform Comparison Tool

From fast and flexible to ultra-high-throughput production power, find the NGS system that's right for you.

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Sequencing Method Explorer

Use this tool to explore experimental sequencing library preparation methods compiled from the scientific literature.

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Infinium MethylationEPIC Kit
Infinium MethylationEPIC Kit

Interrogate over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution.

Infinium Multi-Ethnic Global-8 Kit
Infinium Multi-Ethnic Global-8 Kit

Identify genetic associations with common and rare traits across diverse populations.

Infinium XT
Infinium XT

Perform production-scale targeted genotyping studies on any species with user-defined content.

Infinium Global Screening Array-24 Kit
Infinium Global Screening Array-24 Kit

GSA is a next-generation genotyping array for population-scale genetics, variant screening, pharmacogenomics studies, and precision medicine research.

Extended RAS Panel*

The first FDA-approved NGS in vitro diagnostic for metastatic colorectal cancer for use in establishing eligibility of patients for treatment with Vectibix®.

MiSeqDx Cystic Fibrosis Clinical Sequencing Assay*

FDA-cleared next-generation sequencing assay provides a full view of coding regions of the CFTR gene, to aid in in vitro diagnosis of cystic fibrosis.

MiSeqDx Cystic Fibrosis 139-Variant Assay*

FDA-cleared NGS assay with the largest panel of clinically relevant, functionally validated cystic fibrosis variants in a diverse population.

*For In Vitro Diagnostic Use.

TruSight Tumor 170

Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.

TruSight RNA Pan-Cancer

Study gene expression, variants, and fusions for 1385 oncology genes, in all RNA sample types, including FFPE.

TruSight One Sequencing Panels

Comprehensive panels targeting disease-associated regions of the exome with high analytical sensitivity and specificity.

TruSight Oncology 500

Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.

BaseSpace Sequence Hub
BaseSpace Sequence Hub

An economical and powerful computing environment to manage, analyze, and share data.

BaseSpace Clarity LIMS
BaseSpace Clarity LIMS

A laboratory information management system that helps labs track samples and optimize procedures and workflows.

BaseSpace Variant Interpreter
BaseSpace Variant Interpreter

Enables labs to rapidly annotate, filter, and interpret genomic data.

BaseSpace Correlation Engine
BaseSpace Correlation Engine

Mines genomic studies to get data-driven answers for your research.

Operational Qualification Services

Verify instrument operation and obtain an audit-ready report to help meet regulatory requirements.

Infinium FFPE QC and DNA Restoration Kits

Evaluate sample quality and repair degraded FFPE DNA samples for use in Infinium array-based assays.

cBot 2 Barcoded Strip Tubes

Unique barcodes to seamlessly track samples through the sequencing workflow.