Illumina offers sequencing experimental design software tools to get you started with any sequencing project. Learn more
The future of
BaseSpace Informatics Suite is the unified portfolio of Illumina bioinformatics software solutions. BaseSpace Suite integrates key informatics tools to deliver a seamless user experience that supports complete genomic research and precision medicine workflows. It provides an environment for integrating molecular and clinical data, and permits more people to participate in the discovery process.
BaseSpace Suite guides you from experiment design and sample tracking to data interpretation and meaningful reports. We make it easier to produce high-quality genomic information and apply the results for research, translational, and future precision medicine applications. Use these BaseSpace Suite products together, separately, or with the existing solutions in your lab.
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BaseSpace Sequence Hub enables users to submit sequencing instrument operational data, so Illumina can monitor instrument performance and resolve unforeseen issues.Download Technical Note
BaseSpace Clarity LIMS (formerly Clarity LIMS) is a laboratory information management system that includes preconfigured workflows, and support for regulatory compliance. It offers flexibility to adapt to new workflows, and automation to help your lab scale when sample volumes increase.Learn More
BaseSpace Sequence Hub (formerly BaseSpace) provides scalable and secure storage and analysis of genomic data. Monitor sequencing runs remotely, and share data easily. Our growing ecosystem of BaseSpace Apps simplify data analysis for a wide range of sequencing applications.Learn More
BaseSpace Variant Interpreter (Beta) enables you to rapidly extract biological insight from genomic data within a scalable and secure cloud-based solution. Add rich annotations, filter and interpret variants, and summarize findings into a structured report.Learn More
BaseSpace Cohort Analyzer (formerly NextBio Clinical) enables you to automatically aggregate and analyze subjects with genomics data in a few clicks. Review cohorts for marker frequencies, response, and outcomes. Then share data for biomarker discovery, translational research, and clinical trials.Learn More
BaseSpace Correlation Engine (formerly NextBio Research) enables you to instantly mine over 20,000 genomic studies to get data-driven answers for genes, variants, and signatures. Compare molecular profiles within this curated knowledge base to validate your results and test new hypotheses.Learn More
Go smoothly from experimental design to analysis, annotation, and understanding. Our research informatics tools help you solve challenges – whether you’re a biologist studying microorganisms or a researcher exploring tumorigenesis processes.
Move scientific discoveries from the laboratory through clinical trials and health care for improved health outcomes. Our informatics platforms transform complex genomic data into meaningful insights through integration with curated clinical and phenotypic information.
BaseSpace Correlation Engine and BaseSpace Cohort Analyzer offer powerful analytical platforms to inform drug discovery and development.
Our bioinformatics tools turn data into insight to optimize treatment strategy. Learn more
We provide a robust and scalable platform to aggregate and interpret large-scale genomic data for population sequencing applications in a secure and private environment. Learn more
This genomics computing environment for next-generation sequencing (NGS) data analysis offers a deep set of applications and integration with reporting tools for translational research. Learn more
Aggregate human subjects’ data to enable meaningful insights across the entire drug discovery and development process. Learn more