OUR PRODUCT
XetaBase
XetaBase is a genomic-native tertiary analysis tool, built on the open source Open CB platform – the world’s leading genomic data management solution. In liberating insight from genomic data at scale and speed, XetaBase will help to transform access to precision medicine for millions of people across the world.
As genomic databases move from hundreds of thousands to millions of sequences, XetaBase brings simplicity to increasing complexity with a genomic data management solution developed by and for researchers and clinicians.
Cloud-based and intuitive, XetaBase is configurable to the full spectrum of needs – from research to clinical – across the genomic, biomedical and pharmaceutical industries.
XetaBase enhances the global innovation and collaboration of OpenCB, bringing certification, security, stability and dedicated account support.
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XetaBase allows users to:
Aggregate,
integrate & control
Built on CellBase technologies, XetaBase aggregates over 10TB of reference data from over 20 reference sources – with this number growing all the time. Data is exposed over a single and consistent API: with the ability to integrate this capability into customer infrastructures, where it can be used to manage reference collections.
Store,
retrieve & annotate
Harnessing OpenCGA software, XetaBase can be deployed to store and retrieve genotype data and associated clinical and operational metadata. Integrating with XetaBase’s CellBase functionality provides powerful variant annotation capabilities. It also provides extensive web services, APIs for R and Python, and its own command line interface.
Visualise,
analyse & interpret
Using the powerful IVA web application dashboard tool, users can easily access and visualise variant information stored and annotated within XetaBase. It brings the ability to browse, filter, analyse and interpret – with high levels of customisation to suit user needs.
Visualise,
analyse & interpret
Store,
retrieve & annotate
Aggregate,
integrate & control
Xetabase
Product functionality
XetaBase harnesses database and aggregation techniques to simplify the storage of complex data. Its highly customisable UI fits seamlessly within workflows, integrated directly with the databases instead of using flat files.
XetaBase scales to the demands of genomic data – from a single sample VCF through to hundreds of thousands of whole genomes and billions of variants.
Cuts analysis time to accelerate the application of genomic data in the lab and clinic.
XetaBase is a single system that integrates clinical metadata and variant data by design – data is caller agnostic, making it accessible, manageable and manipulable – to generate greater insight.
Data is aggregated on a per customer basis to uncover previously inaccessible insights. The more data a customer loads, the more powerful insights become.
XetaBase is run, supported and maintained on a reliable and responsive infrastructure – with support models designed to customer needs – in both the research and clinical settings.
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XetaBase results
Efficiency
- Single platform consolidation increases operational efficiency.
- Reduces time devoted by clinical scientists to case interpretation, speeding up diagnosis and increasing diagnostic yield.
- Real time interrogation of data in a variety of ways, with no need to reload or reprocess data, restart the analysis or rebuild the dataset.
