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Our most powerful sequencing platform, with scalable throughput and flexibility
Kits & Reagents
A fast, integrated workflow for a wide range of applications
Selection & Planning Tools
Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, or cDNA in as little as 90 minutes
Software & Informatics Products
Provides accurate, ultra-rapid secondary analysis of sequencing data
Verify instrument installation and operation, obtain an audit-ready report
Popular groupings designed for your applications
Resources to help you design, run, and evaluate your sequencing project
Shares views on actions needed to bring genomics to the patients who need it
All Investor Information
Illumina upgrade solution available across all active systems
All Support Tools
Product Support Services
FFPE-compatible panel for measuring T cell diversity and clonal expansion in tumor samples
Cancer Genomics Products
Microbial Genomics Research
Featured workflow: microbial whole-genome sequencing
Microbial Genomics Products
How genomic selection has improved breeding plans
Optimized for population-scale genetics, variant screening, pharmacogenomics studies, and precision medicine research.
Complex Disease Research Products
Target multiple variant types, including TMB and MSI
Offers comprehensive detection of rare chromosomal conditions
Podcast Episode 47: One child's rare disease and the impact of NGS-based testing on her family
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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