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Cost-efficient flexibility for new and emerging applications
Kits & Reagents
Enabling comprehensive genomic profiling from FFPE with up to 192 samples per flow cell
Selection & Planning Tools
Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, or cDNA in as little as 90 minutes
Software & Informatics Products
Pay-as-you-go or purchase larger quantities at a lower price point for high-throughput data analysis applications
Obtain an audit-ready report to help meet regulatory requirements
Find popular product groupings for your workflow
Q&A with Chief Medical Officer Phil Febbo, MD
Next-generation sequencing changes everything in the fight against COVID-19
All Investor Information
Procedure for novel coronavirus (2019-nCoV)
All Support Tools
Product Support Services
Cancer Research Products
Microbial Genomics Research
NGS offers a hypothesis-free research method for use with viruses (such as COVID-19) and other microbes
Microbial Genomics Products
A highly sensitive and accurate tool for measuring expression across the transcriptome
Powerful tools for studying the transcriptome in an unbiased manner from minimal input
Complex Disease Research Products
VeriSeq NIPT: The new standard in prenatal screening
Reproductive Health Products
Two cystic fibrosis assays now available in one convenient library prep
Genetic Health Products
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Cost-efficient flexibility for new and emerging applications.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
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.
Find the system guide, site prep guide, indexed sequencing guide, and other supporting documentation.
Online Illumina sequencing courses are free, interactive, and available any time.
Don’t let your budget hold you back. Explore different buying options to find which best fits your needs.
Generate your own customized documentation, specifically tailored to your experiment.
Additional information about sequencing quality scores, how they are calculated, and the relationship between sequencing quality score and base call accuracy.
Learn how to estimate and achieve the necessary sequencing coverage for your experiment.
See our best practices for generating high-quality data from human whole-genome sequencing on the NovaSeq 6000 System.
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