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.
Data sharing allows you to publish and collaborate with speed.
Access resources and solutions to help simplify your informatics infrastructure and data analysis pipeline setup.
Explore infrastructure & pipeline setupAutomate workflows, integrate instruments, and manage samples with ease.
Learn more about LIMSpromo

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 Multiomics is a fully integrated multiomic and multimodal analysis software from Illumina, enabling seamless sample-to-insight workflows. Researchers can explore multiomic data, reveal deeper biological insights, and accelerate discoveries. With this comprehensive cloud-based platform, biologists can generate powerful statistics and interactive visualizations—no bioinformatics background required.
Learn more about Illumina Connected MultiomicsOur 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. For tertiary analysis, our data interpretation tools empower researchers to turn sequencing data into biological insights.
Learn more about NGS data analysisBioinformatics 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 about biological data interpretationOur 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.
See all Illumina software
| Panel Design | Sample & Workflow Management | Instrument Run Setup & Management | Genomics Run & Monitoring |
|---|---|---|---|
| Secondary Data Analysis | Data Management & Collaboration | Interpretation & Case Reprting | Translational Research | ||||
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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.
Access high-quality, freely available software designed by trusted Illumina engineers and partners. Access Illumina GitHub
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.
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Product files and installable software for use with Illumina products.
A cloud-based multiomic analysis and interpretation software that enables sample-to-insight workflows with visualizations, scalability, and secure data management.
A comprehensive cloud-based genomics data platform for secure data management, infrastructure scalability, and bioinformatics workflow implementation.
Emedgene software streamlines variant interpretation for rare disease genomics and other germline research applications with explainable AI and automation.
Illumina DRAGEN (Dynamic Read Analysis for GENomics) secondary analysis 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.
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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.