NovaSeq 6000 Sequencing System is by far our most powerful instrument, designed to adapt to your needs.
Kits & Reagents
Improved Q30 score, support for UMIs, extended shelf life, and support for Illumina DNA PCR-Free Library Prep
Selection & Planning Tools
A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
Software & Informatics Products
DRAGEN v3.9 release now available with multi-cloud support, accuracy improvements and more
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
Find popular product groupings for your workflow
Our leaders are pioneers of genetic research and clinical applications. They are deeply committed to scientific accessibility, data, and community.
Next-generation sequencing is helping Native nations with sovereignty and genetic research
All Investor Information
New page replaces MyIllumina Technical Updates email
All Support Tools
Product Support Services
Maximize identification of molecularly matched therapies with one biopsy, one test, one report
Cancer Research Products
Microbial Genomics Research
With the debut of the COVIDSeq Assay, smaller labs are participating in surveillance
Microbial Genomics Products
Identifying variants could help select highly productive breeds that adapt to rapidly changing climates
The most comprehensive genotyping microarray on the market for pharmacogenomic research now at 25% off, restrictions apply
Complex Disease Research Products
Comprehensive genomic profiling is driving innovation across the 51-hospital system
The collaboration will introduce VeriSeq NIPT Solution v2 in Southeast Asia
Reproductive Health Products
Illumina supports the release of a landmark consensus on whole-genome sequencing in the diagnosis of genetic diseases in newborns
Genetic Health Products
Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study.
Genet Med 18 231-8 2016
Clinical Sensitivity of Cystic Fibrosis Mutation Panels in a Diverse Population.
Hum Mutat 37 201-8 2016
Next-Generation Molecular Testing of Newborn Dried Blood Spots for Cystic Fibrosis.
J Mol Diagn 18 267-82 2016
Information about instrument components and software, performing a sequencing run, and maintenance.
Preparing a lab for the MiSeqDx Platform: lab space, electrical, and bench requirements, and user-supplied consumables.
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.
User guide, safety guide, site preparation guide, and related application and tech notes for the MiSeqDx instrument.
These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantitation.