Our software platforms are the solutions you need to aggregate, interrogate, and share data to achieve scientific breakthroughs
Next-generation sequencers generate massive amounts of data. When you have the right bioinformatics tools, you can aggregate this data, interpret it, and socialize the information quickly.
The Illumina software suite offers data solutions that support genomics research and clinical research from setup to analysis. We embrace changing technology and defy the barriers that challenge innovation.
Adopt lab automation to improve efficiency.Learn More
Data sharing allows you to publish and collaborate with speed.
See what a LIMS can do for you.Learn More
Simplify how you import biological sample information, design and pool libraries, prepare sequencing runs, and much, much more.See How
Automate workflows, integrate instruments, and manage samples with ease.Explore the Technology
Options for every kind of data analysis imagineable.Browse the Formats
A robust, enterprise-grade, versatile platform empowering omics workflows, scalability, global compliance, and data science tools.
In this webinar, bioinformatics experts discuss multiomics dataset integration challenges, tools used, the impact of multiomic data integration on research, and more.
Learn how cloud-based genomic data solutions can store, process, and share large NGS and genomic datasets with greater speed, scalability, and security.
Illumina Connected Analytics breaks down the barriers of data silos by delivering versatile and integrated data science tools that enable high-volume automated multi-omics workflows and operations.Learn More
Our sequencers come equipped with primary data analysis tools built in. For secondary analysis, our bioinformatics tools align and assemble DNA and RNA fragments to fully sequence a sample so that genetic variants can be determined quickly and effectively.Learn More
Bioinformatics software and biological data mining drive insights into fundamental biological processes and the causes of genetic disease. Use our tools to interpret biological variants, understand population data, and employ focused sequencing applications for drug discovery, cancer research, single-cell analysis, and more.Learn More
Our software ecosystem provides solutions that span across workflows. From specific applications to secondary and tertiary analysis, our seamless software portfolio enables you to hit development milestones faster.
|Panel Design||Sample & Workflow Management||Instrument Run Setup & Management||Genomics Run & Monitoring|
|Secondary Data Analysis||Data Management & Collaboration||Interpretation & Case Reprting||Translational Research|
Get API, application, and developer documentation as well as access to binary downloads and installers so that you can collaborate with other developers and have conversation to make the most of your data.
A collaborative space to exchange ideas, tips, and techniques to empower your data analysis and interpretation. Learn More
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DRAGEN, Instrument, Informatics, New to NGS, Microarray, General Topics
Access high-quality, freely available software designed by trusted Illumina engineers and partners. Learn More
Access APIs to subscribe to platform events and specify delivery targets for receiving.
Direct access to developer resources for next-generation sequencing, analysis, and data science.Visit Portal
Learn how to get started, read about our native apps, SDKs and sample apps, developer tools, and more.
Find documentation, FAQs, technical bulletins, training, software downloads, and other resources in our Support Center.
Product files and installable software for use with Illumina products.
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A robust, enterprise-grade platform that empowers multi-omics workflows, on-demand scalability, and integrated data science tools.
This software as a service (SaaS) analytics solution integrates with BaseSpace Sequence Hub and is compatible with systems used for rare disease research.
The Illumina DRAGEN (Dynamic Read Analysis for GENomics) Bio-IT Platform provides accurate, ultra-rapid secondary genomic analysis of sequencing data.
Data management and simplified bioinformatics for labs getting started and for rapidly scaling next-generation sequencing operations.
This laboratory information management system helps genomics labs track samples, manage workflows, and automate routine tasks.