NGS data analysis, storage, and collaboration made easy Welcome to push-button informatics
BaseSpace is the Illumina genomics computing environment for next-generation sequencing (NGS) data analysis and management. This flexible solution is available as both a cloud bioinformatics and onsite bioinformatics solution. Now sequencing labs can easily and securely analyze, archive, and share sequencing data, and researchers can simplify and accelerate NGS data analysis with push-button tools.
BaseSpace offers a wide variety of NGS data analysis apps (tools). These include:
Together, these apps cover the common data analysis methods used with Illumina sequencing data. These methods include RNA-Seq, exome /enrichment, amplicon, whole-genome sequencing (WGS), de novo assembly, and 16S metagenomics.
Key features of BaseSpace, besides NGS data analysis, sample/run management, and cloud bioinformatics or onsite options, include:
BaseSpace makes sample and run management easy using the Prep tab feature for the NextSeq 500 Sequencing System. The Prep tab is an intuitive, graphical environment for one-stop library and run preparation.
The BaseSpace Onsite System is a local version of the BaseSpace cloud bioinformatics solution that enables you to safely and securely store, share, and analyze NGS data from the NextSeq 500 System on site.
BaseSpace Support Find user guides, app release notes, and additional technical information. Access BaseSpace Support
Getting Started with BaseSpace View Video Learn how to get started with push-button bioinformatics in BaseSpace.
BaseSpace Onsite Platform View Video BaseSpace allows users to access their next-generation sequencing data anywhere .
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