Science That Doesn't Cut Corners

Every GeneLens report is built on published genetics research, independently reviewed, and updated when the evidence changes.

CLIA Certified

Our partner laboratory holds Clinical Laboratory Improvement Amendments (CLIA) certification - the federal standard for high-complexity genetic testing in the United States.

HIPAA Compliant

Your genetic data is treated as protected health information under HIPAA. We implement encryption at rest and in transit, with strict access controls and audit logging.

Peer-Reviewed Basis

All health and pharmacogenomics reports cite the primary literature used to establish each association. You can review the studies that back your results.

Genotyping Method

Microarray Genotyping at Scale

GeneLens uses high-density SNP microarray genotyping to analyze over 700,000 positions in your genome. This method has been the industry standard for consumer genetics for over a decade - well-characterized, reproducible, and highly accurate.

Your raw sample undergoes extraction, amplification, hybridization, and scanning before the data reaches our interpretation pipeline. Each step includes quality control checkpoints. Samples that don't meet our minimum call rate threshold are flagged for re-extraction.

  • 99.6% genotyping call rate
  • Dual-strand verification for critical health variants
  • Orthogonal validation against reference databases
Lab equipment / microarray chip visualization  -
Data Interpretation

From Genotype to Insight

Raw genotype data doesn't mean much without rigorous interpretation. Our algorithms compare your variants against curated databases - including ClinVar, GWAS Catalog, and PharmGKB - to generate your reports.

For ancestry analysis, we use a reference population panel spanning over 200 groups worldwide, built from public and licensed datasets. Admixture estimates are computed using validated population genetics methods.

  • Reports cite specific SNPs and effect sizes
  • Population frequency data included for context
  • Confidence intervals shown where applicable
Data interpretation pipeline diagram  -
Privacy Architecture

Your Data, Controlled by You

We don't sell your genetic data. We don't share it with insurers, employers, or third-party advertisers. Period. Your genome is de-identified in storage and linked to your account only through a secure identifier.

You can delete your data at any time from your portal settings. Deletion is complete - raw sample, processed genotype data, and reports. We retain only the minimum records required for legal compliance for 30 days following deletion requests.

  • No data sales - ever
  • Full deletion on request
  • Research sharing is opt-in only
  • Annual third-party security audits
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Questions About Our Methods?

Our science team reads every inquiry. If you have questions about a specific report methodology, we respond with citations, not talking points.

Contact the Science Team