A bioinformatics software suite connecting your entire genomics workflow
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.
Proven accuracy
Attain high-quality, reproducible insights using DRAGEN, most comprehensive and leading accuracy for germline and somatic variant calling as measured by PrecisionFDA1.
Integrated and efficient
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.
Trusted technology
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.
Software product portfolio
From wet lab to data insights, the Illumina software product portfolio offers solutions for every workflow stage
Wet lab
Lab
Run
BaseSpace Sequence Hub
Streamlined cloud-based run setup and monitoring.
Illumina Run Manager
Intuitive on-instrument run setup and monitoring.
Dry lab
Analytics
DRAGEN
The most accurate and comprehensive secondary analysis for next-generation sequencing optimized for efficiency1.
Illumina Connected Analytics
Operationalize bioinformatics workflows with sequencer integration, automatic analysis of customizable workflows, or out-of-the-box DRAGEN pipelines.
BaseSpace Apps
Push-button analysis with direct sequencer integration.
Insights
Emedgene
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.
Connected Insights
Streamline user-defined data interpretation workflows and report generation for somatic oncology and soon hereditary diseases, leveraging extensive third party knowledge sources.
Correlation Engine
An interactive omics knowledgebase that puts private omics data in biological context with highly curated public data.
Discovery and diagnostic power
Genomic analysis solutions for any size experiment
Clinical research
For investigating a sample for a known genotype-phenotype association
Experiment level
Discover new genotype-phenotype associations with software customizable to accelerate new insights
Trial or population genetics
Highly accurate and efficient analysis completely customizable for large scale genomics analysis and discovery at scale
Customer stories
Can genomics stop the world’s leading cause of death?
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.
Using whole-genome sequencing to study early-onset Parkinson’s disease
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.
Streamlined workflow management enables sequencing at scale
Implementation of BaseSpace Clarity LIMS Software enables Rapid Novor to future-proof their growing laboratory operations.
Focused Workflows for key applications
We support workflows in the following areas for in-depth analysis of clinical and research data:
Oncology
Identify relevant DNA and RNA variants in tumor types and conduct in-house comprehensive genomic profiling of tumor samples.
Rare disease
Discover variants associated with rare disease through our AI-powered software. Offers support for genomes, exomes, panels, and virtual panels.
Reproductive health
Obtain accurate and informative NIPT results from Illumina VeriSeq.
Infectious disease
Detect and characterize infectious diseases like COVID-19 with powerful, easy-to-use software analysis.
Software documentation and resources
Visit the Software Resources Portal to access documentation, developer resources, and software news and updates
Visit Portal
Support and documentation
Get documentation, FAQs, technical bulletins, training, developer tools, and software downloads—all in one place.
Blog
Visit our Informatics blog for the latest product news, updates, and more.
Interested in learning how informatics software can streamline your entire data workflow? Fill out the form and we’ll be in touch.
Proven industry leadership and innovation
Your trusted implementation and support partner
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.
Data security and compliance
High standards of data privacy and protection
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.
Related content
Scaling to the cloud to support sequencing
DRAGEN platform on Microsoft Azure provides ultra-rapid secondary analysis capabilities in the cloud, enabling adoption of high-throughput whole-genome sequencing.
Using analytics to improve cancer diagnosis and therapy selection
Developing and automating best-practice workflows that make analyzing, processing, and disseminating genomic data more accessible.
Bringing bioinformatics pipeline in-house reduces costs and decreases turnaround time
Phosphorus uses the DRAGEN Bio-IT Platform to perform genomics data analysis onsite and at an accessible price point.
Additional Software
DesignStudio Custom Assay Designer
This web-based assay design tool helps scientists design custom targeted sequencing panels and create custom genotyping microarray assays.
Correlation Engine
Extend your research by mining scientific studies to get data-driven answers for genes, experiments, drugs, and phenotypes.
Polygenic Risk Score Software
This user-friendly research software simplifies the process of polygenic risk score calculation, analysis, and reporting with an easy-to-use interface.
References
- DRAGEN on Illumina is the first single platform to achieve 99.83% accuracy based on PrecisionFDA v2 Truth Challenge Benchmark Data. Details here.