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Kits & Reagents
Use these components in ATAC-Seq experiments to analyze chromatin accessibility
Selection & Planning Tools
Take your research further with the right sequencing panels or microarrays for your project
Software & Informatics Products
Provides accurate, ultra-rapid secondary analysis of sequencing data
Hands-on training with expert instructors or online courses to fit your schedule
Find popular product groupings designed for your research focus and instrument
RNA-Seq and HLA typing are increasing the power and efficiency of a target discovery platform
Helping Students Nationwide Learn the Real-World Impacts of Genomics
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Upgrade solution for Illumina systems
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Product Support Services
Illumina to collaborate with the Frederick National Laboratory for Cancer Research
Cancer Genomics Products
Microbial Genomics Research
A fast, integrated workflow for a wide range of applications
Microbial Genomics Products
Deadline for 2020 Agricultural Greater Good Initiative grant applications is December 6
Discover how genetic variants and PRS could enable more effective treatment of genetic conditions.
Complex Disease Research Products
Assay targeting multiple somatic variant types from plasma, including TMB and MSI
Learn how noninvasive prenatal testing (NIPT) is making an impact around the world.
Consortium aims to expand access to clinical whole-genome sequencing for genetic diseases
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
Find tools to help you choose the right products for your needs and plan your experiments. Identify the right library prep kit or microarray, calculate sequencing coverage, explore methods compiled from publications, design custom assays, and more.
This guide contains an overview of instrument components and instructions for operating and maintaining the MiniSeq System.
This guide contains lab specifications and requirements for preparing the lab for the MiniSeq System.
Online Illumina sequencing courses are free, interactive, and available any time.
This tool will help you determine the best hands-on sequencing training for your needs based on your area of interest, application, library preparation kit, and platform.
Sequencing coverage describes the average number of NGS reads that align to known reference bases. Coverage requirements vary by application.
Additional information about sequencing quality scores, how they are calculated, and the relationship between quality score and base call accuracy.
Find system guides, related application and technical notes, and other supporting documentation for the MiniSeq System.
These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantitation.
The Custom Protocol Selector enables you to generate your own customized documentation, specifically tailored to your experiment.
Discover how the simple, affordable MiniSeq System makes sequencing an everyday tool for labs of any size.
Mattia Prosperi, PhD, will use his MINI Cooper and MiniSeq to study the spread of mosquito-borne pathogens in Florida.
Hongmei Li-Byarlay, PhD, describes how she will use the MiniSeq to study the honeybee.
Una McVeigh discusses how the MiniSeq System will help her identify new genetic variants associated with breast cancer.
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