Informatics Products
Bring your genomics data to life
Enabling breakthrough discoveries with clinical and translational applications
To unlock the next wave of omics discovery we must analyze, manage, aggregate, mine, and explore data more efficiently. Now, we can.
Learn MoreThe Illumina software and informatics portfolio includes some of the fastest, most accurate, and advanced solutions for analysis, interpretation, and data aggregation. Our comprehensive software, informatics, and data solutions stand alongside Illumina sequencers to offer:
| Panel Design | Sample & Workflow Management | Instrument Run Setup & Management | Genomics Run & Monitoring |
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| Secondary Data Analysis | Data Management & Collaboration | Interpretation & Case Reprting | Translational Research | ||||
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A simple and powerful method for evaluating loci and creating successful custom genotyping array and sequencing panels.
Laboratory information management system to help genomics labs track samples and manage workflows.
The platform for ultra-rapid secondary genomic analysis with highly accurate reults, diverse applications, and frequent updates. DRAGEN can process NGS data for an entire human genome at 30x coverage in about 25 minutes. Now with DRAGEN ORA compression technology, DRAGEN can losslessly compress FASTQ files up to 5x.
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Software designed for better understanding and potential solutions in rare disease. With ultra-rapid variant calling, simplified case management, intuitive interpretation mechanisms, and a secure environment, TSS drives standards in sequencing discovery.
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Built for high-volume multi-omics operations limited by data silos and a lack of bioinformatics and data science tools. Illumina Connected Analytics delivers a robust, enterprise-grade, versatile platform empowering automated omics workflows, on-demand scalability, integrated data science tools, designed with data privacy and security in mind.
Cloud based run planning and simplified bioinformatics for labs that are getting started and rapidly scaling next-generation sequencing.
LoginOrganize and manage sample inputs and structure data outputs to fit your research needs
Perform rapid, rich, and accurate annotation of genomic data for individual subjects.
Gain access to one of the largest biological databases in the world to get data-driven answers for genes, experiments, drugs and phenotypes.
Integrate and analyze subject and genomic data together using innovative visualization and analysis tools.
We support the following workflows for in-depth research and data analysis in key applications
TSS v2.0 incorporates a seamless integration with sequencers and BaseSpace SequenceHub, as well as an integrated AI-based variant prioritization tool. The updated TSS workflow reduces interpretation time and allows users to explore variants associated with rare disease.
Access API, application, and developer documentation as well as binary downloads and installers. Collaborate in real-time with like-minded collegues.
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Find support, submit requests, and join in on conversations about your work. Learn More
Get documentation, FAQs, technical bulletins, training, and software downloads all in one place. Learn More
Access high-quality, freely available software designed by trusted Illumina engineers and partners.
Learn how to get started, read about our native apps, SDKs and sample apps, developer tools, and more.
Product files and installable software for use with Illumina products.
SubscriptionOne easy annual fee with tiered access Tiers based on:
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ConsumptionScale up or down, depending on your needs Choose your amounts of:
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Add-onsIncrease capabilities with individual features Product specific customization:
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| Illumina Connected Analytics | |||
| BaseSpace Clarity LIMS | |||
| BaseSpace Sequence Hub | |||
| DRAGEN-Bio IT Platform | |||
| TruSight Software Suite |
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Whole-genome and whole-exome sequencing-based consumer genomics companies are entering the market, offering a genomic view for life-long genetic assessment.
Illumina Connected Analytics enables automated workflows that help the Genomics Platform Group at UMCCR analyze, process, and disseminate genetic data.
Sano Genetics protects individual genetic information ownership while connecting people to meaningful research.