Built for speed, scale, and insights, Illumina Connected Analytics meets the biggest challenges in data engineering. This versatile bioinformatics platform is fully integrated with Illumina sequencing platforms and harnesses the power of DRAGEN. Ready to transform your data bottleneck into a catalyst for scientific discovery?
Learn More Request InfoAttain high-quality, reproducible insights using DRAGEN, most comprehensive and leading accuracy for germline and somatic variant calling as measured by PrecisionFDA1.
Minimize hands-on time and seamlessly connect data from across your entire workflow. Illumina software is built for deep sequencer integration and efficient scaling in order to meet your data needs.
Reduce bioinformatics bottlenecks and streamline your entire workflow. Illumina is committed to relentless innovation, creating new bioinformatics technologies that expand access to genomics for all.
Streamlined cloud-based run setup and monitoring.
Intuitive on-instrument run setup and monitoring.
The most accurate and comprehensive secondary analysis for next-generation sequencing optimized for efficiency1.
Accurate, comprehensive and efficient secondary analysis for Infinium array-based assays.
Operationalize bioinformatics workflows with sequencer integration, automatic analysis of customizable workflows, or out-of-the-box DRAGEN pipelines.
Push-button analysis with direct sequencer integration.
Enable high efficiency data interpretation workflows for germline research WGS, WES, and panels, with the support of explainable AI (XAI) and user-configured automation to maximize scale potential.
Streamline user-defined data interpretation workflows and report generation for somatic oncology and soon hereditary diseases, leveraging extensive third party knowledge sources.
An interactive omics knowledgebase that puts private omics data in biological context with highly curated public data.
This eBook provides an overview of Illumina Connected Software solutions that can maximize the discovery power of your transcriptomics and epigenomics research.
Download eBookFor investigating a sample for a known genotype-phenotype association
Discover new genotype-phenotype associations with software customizable to accelerate new insights
Highly accurate and efficient analysis completely customizable for large scale genomics analysis and discovery at scale
Prof. Dr. Andreas Ziegler, scientific director and CEO of Cardio-CARE, uses genomics to study cardiovascular disease and population health data with a clinical focus.
NysnoBio uses Illumina Connected Analytics and Cohorts to analyze NGS data and enable development of a gene therapy to slow Parkinson's Disease progression in individuals under age 50.
Implementation of Clarity LIMS Software enables Rapid Novor to future-proof their growing laboratory operations.
Identify relevant DNA and RNA variants in tumor types and conduct in-house comprehensive genomic profiling of tumor samples.
Discover variants associated with rare disease through our AI-powered software. Offers support for genomes, exomes, panels, and virtual panels.
Obtain accurate and informative NIPT results from Illumina VeriSeq.
Detect and characterize infectious diseases like COVID-19 with powerful, easy-to-use software analysis.
Visit the software resources portal to access documentation, developer resources, and software news and updates
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llumina software solutions are built with the same exceptional level of accuracy, accessibility, and security standards as our sequencing solutions. Our comprehensive bioinformatics suite maximizes efficiency and empowers you to transform your data into insights with powerful tools
for configuration, seamless instrument integration, and approachable user experiences. To help you get up to speed faster, we offer best-in-class implementation support accelerating your utilization of genomics data.
To meet the most stringent security requirements, our software products are built with the following security and compliance certifications in mind. Data sharing security and governance, audit trails with encryption, and controlled sharing ensure your data is kept safe and secure. See informatics product pages to understand product-specific compliance and security certifications.
DRAGEN platform on Microsoft Azure provides ultra-rapid secondary analysis capabilities in the cloud, enabling adoption of high-throughput whole-genome sequencing.
Developing and automating best-practice workflows that make analyzing, processing, and disseminating genomic data more accessible.
Phosphorus uses the DRAGEN Bio-IT Platform to perform genomics data analysis onsite and at an accessible price point.
This web-based assay design tool helps scientists design custom targeted sequencing panels and create custom genotyping microarray assays.
Extend your research by mining scientific studies to get data-driven answers for genes, experiments, drugs, and phenotypes.
This user-friendly research software simplifies the process of polygenic risk score calculation, analysis, and reporting with an easy-to-use interface.