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Enable comprehensive genomic profiling with accurate and comprehensive homologous recombination deficiency assessment
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Discover novel trait and disease associations with optimized tag SNPs and functional exonic content at an attractive price
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DRAGEN v4.0 release enables machine learning by default, providing increased accuracy out of the box
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
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Whole-exome sequencing kit with library prep, hybridization reagents, exome probe panel, size selection beads, and indexes
See what is possible through the latest advances in high-throughput sequencing technology
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View the unveiling of our newest technologies and products on-demand, recorded live at the Illumina Genomics Forum
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Monitor SARS-CoV-2 variants and other respiratory viruses in the community
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Mapping genetic diversity to identify where confiscated gorillas come from and boost survival rates
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Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation
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Comprehensive, IVD, in-lab aneuploidy screening solution for accurate NIPT results in 26 hours
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Whole-genome sequencing (WGS) for rare disease offers key advantages over other genetic testing methods
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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.