Integrate your scientific and clinical research data across the entire workflow, from samples and systems to analysis. Our accurate, approachable, and comprehensive suite of bioinformatics solutions enable you to unlock the full power of your data to improve human health.
Attain 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.
The most accurate and comprehensive secondary analysis for next-generation sequencing optimized for efficiency1.
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.
For 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
Cardiovascular disease (CVD) is the world's leading cause of death. To tackle the issue, Prof. Dr. Andreas Ziegler, scientific director and CEO of Cardio-CARE, is using genomics to study population health data with a clinical focus.
NysnoBio is using 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 the age of 50.
Implementation of BaseSpace 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.
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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.