Rapidly extract and report biological insight from genomic data

BaseSpace Variant Interpreter (Beta)

Introducing the Newest Addition to BaseSpace Suite

BaseSpace Variant Interpreter (Beta) enables you to perform rapid annotation, filtering, and interpretation of genomic data. Customize workflows and summarize findings into structured reports. Determine biological significance of genomic variants within a software framework focused on data security, compliance, and operational efficiency.

This cloud-based variant interpretation platform offers:

  • User-Friendly and Efficient Variant-to-Report Workflow: Seamless integration with BaseSpace Sequence Hub, and data transfer with an intuitive user interface.
  • Rapid, Rich, and Accurate Annotation: Comprehensive annotation of genomic data from a broad range of sources.
  • Increased Lab Operational Efficiency and Scalability: Customizable workflows for all assay types, from whole-genome sequencing to targeted sequencing. Workgroups support admin-assigned user roles and permissions.
  • Support for Security and Lab Compliance: Security features include access control, audit trail, and test configuration.
  • Accelerated Variant Interpretation with BaseSpace Knowledge Network: Integrated knowledge base containing genotype-phenotype associations.

BaseSpace Variant Interpreter (Beta) uses Amazon Web Services that are ISO 27001 certified.

BaseSpace Variant Interpreter

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Additional Resources

BaseSpace Variant Interpreter (Beta) Flyer

View PDF Rapidly extract and report biological insight from genomic data.

BaseSpace Variant Interpreter (Beta) Data Sheet

View PDF Learn more about the workflows, annotations and security and lab compliance features.

BaseSpace Knowledge Network Tech Note

View PDF Variant interpretation is simplified with organized biomarker content curated from large public databases.