Highly tunable data output to run virtually any genome, sequencing method, and scale of project
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A rapid, single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA.
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Cloud-based variant interpretation
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Bringing efficiency and high confidence to case management, variant analysis, and interpretation in rare disease
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
Find popular product groupings for your workflow
Whole-genome shotgun sequencing and transcriptomics provide data to refine drug discovery and development
TruSight Software Suite accelerates identification of genetic diseases
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Three approaches to help researchers with sequencing
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Expanded portfolio enables comprehensive genomic profiling from blood and tissue
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Microbial Genomics Research
A culture-free method for studying complex microbiomes or environments
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A highly sensitive and accurate tool for measuring expression across the transcriptome
TruSight Software Suite accelerates the identification of genetic diseases
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Study gene expression changes in cancer, RNA biomarkers of drug response, and more
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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.
This webinar provides an introduction to the MiniSeq System and its simple, streamlined workflow.
Learn how comprehensive tumor profiling with NGS can help you avoid costly and time-consuming iterative testing.
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