From question to answer, faster.
Helix Explorer is the premier enterprise genomic analysis and operations platform. It brings cohort building, population-scale genomic analysis, and AI assistance into one governed, compliance-ready environment to drive research.
Book a Demo30-second product tour
Start with a research question.
Describe the cohort and the analysis you want to create.
Overcome clinicogenomics bottlenecks in one platform
Self-serve genomic cohort building
Helix Explorer enables self-serve genomic cohort building with no-code interfaces and natural language querying, in minutes.
Population scale genomic analysis
Genomic-scale work makes variant analysis slow and costly. Built on Databricks Unity Catalog, Explorer delivers high-performance population scale genomic analysis with prebuilt workflows for GWAS, PheWAS, and gene burden testing.
Governed genomic trusted research environment
Explorer provides a hosted genomic trusted research environment with built-in role-based access controls, audit logging, and row-level security from day one.
One environment for every stage of research
Explorer houses the applications your team needs to go from cohort to insight, without leaving the platform.
No-code and AI-assisted cohort creation. Streamline genomic cohort building to create a research-ready cohort in minutes using demographic, clinical, and genomic criteria, or describe your population in plain language.
Learn more about Cohort Builder
13+ years
Linked EHR history across participants, 100% consented for recontact
Explorer MCP
Powered by Claude Science, the GenoSphere™ MCP connector enables researchers to explore de-identified, population-level human genetics and health data directly from the GenoSphere research dataset using natural language.
Researchers, clinical scientists, and life-sciences teams can instantly query dataset coverage, variant frequency, or cohort condition prevalence without writing SQL or navigating complex internal schemas. Claude interfaces directly with Helix, translating conversational prompts into aggregate, actionable statistics.
GenoSphere™ Data
GenoSphere™ datasets deliver deeply curated de-identified, clinicogenomic data by pairing Exome+® sequencing with an average of 13 years of longitudinal electronic health record (EHR) data, further enriched by medical and pharmacy claims.
Purpose-built to accelerate precision medicine, these datasets empower life sciences organizations across a wide range of therapeutic areas.
Built for every researcher
Built for every researcher in the building
Configurable, role-based access controls that map to your organization's existing research permissions.
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Health systems
Self-serve access to your own population's data and broader HRN data for population health and precision medicine research.
Ready to see what Explorer can do for your research?
Connect with our team to see how Explorer can accelerate your research, from cohort to insight.
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