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The most affordable Illumina system, designed for everyday sequencing
Kits & Reagents
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information
Find specifications and project recommendations for kits such as Nextera XT DNA using the Kit Selector tool
Software & Informatics Products
Mine over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research
Verify instrument installation and operation, and obtain an audit-ready report
Reagent kits for the NovaSeq 6000 System provide ready-to-use cartridge-based reagents for cluster generation and SBS
Low NovaSeq 6000 System sequencing costs spark new projects and customer growth
Survey finds Americans unaware of DNA's power to improve lives
Complimentary and secure instrument monitoring can help you avoid unplanned downtime
All Support Tools
Product Support Services
Deep, comprehensive, and accessible sequencing power for detecting solid tumor biomarkers
Cancer Genomics Products
Microbial Genomics Research
Local scientists analyze transmission patterns and trace origin of Ebola outbreak in the Democratic Republic of Congo
Microbial Genomics Products
A rapidly emerging method for studying biodiversity and monitoring ecosystem changes
Complex Disease Research Products
Families facing rare diseases often spend years pinpointing the problem in solitude – until now
In podcast episode 41, Dr. Åke Borg discusses developing better biomarkers for risk stratification of individuals with breast cancer
Rethink prenatal screenining. Think VeriSeq NIPT.
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.
Use this guide to help you evaluate important factors and choose the right next-generation sequencing instrument for your lab.
This interactive tool will help you compare sequencers and find the one that’s right for your lab or application.
Compare the iSeq 100 System with other Illumina benchtop sequencers.
This detailed overview describes the basics of Illumina sequencing technology, key methods, and more.
See Illumina sequencing by synthesis (SBS) technology in action and learn how it works.
Learn the key differences between NGS and Sanger sequencing and determine when NGS can be a more effective option.
Compare the benefits of NGS technology to qPCR and learn which one to choose.
Find kits, methods, and automation solutions to help you prepare DNA or RNA libraries before sequencing.
Our software simplifies sequencing data analysis, so you can focus on your research instead of setting up analysis workflows.
Learn how targeted NGS can help you gain greater insight in your studies and save time compared to traditional methods.
See how sequencing on a semiconductor chip reduces instrument cost and simplifies NGS on the compact iSeq 100 System.
Explore different buying options—including leasing, bundles, trade-in offers, and more—to find one that fits your needs.
This document offers specification information and other resources to help you justify funding for the iSeq 100 System.
Acquire the advanced technology you need now through fast, easy, and affordable financing and leasing programs.
Find supporting documentation for the iSeq 100 System.
Online Illumina sequencing courses are free, interactive, and available any time.
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.
These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantification.
New to Illumina technology? See step-by-step guidance to help you transition your studies.
Find workflow guidance from Illumina experts, including considerations for hotspot resequencing with AmpliSeq for Illumina Cancer Hotspot Panels.
View tips on transitioning to the Nextera DNA Flex Library Prep Kit, including considerations for viral and bacterial whole-genome sequencing.
See our detailed guides designed to help you transfer projects from TruSeq Custom Amplicon to AmpliSeq for Illumina panels.
Determine the best sequencing library preparation kit for your needs based on your project type, starting material, and method of interest.
Identify sequencing panels that target your genes of interest.
Find interactive tools designed to help you choose the right products for your needs and plan your experiments.
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