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Welcome to GeneBe

GeneBe is an innovative platform dedicated to genetic variant interpretation. Pronounced as "gene bee" (/dʒiːnbiː/), it aims to solve the challenges of genetic variant annotation and interpretation by providing a fast, reliable, and user-friendly solution.

Our Mission​

At GeneBe, we strive to make genetic variant analysis accessible and efficient for researchers, clinicians, and geneticists. Our platform aggregates data from various reputable sources, offering:

  • Comprehensive Variant Information: Including variant function, GnomAD frequencies, ClinVar annotations, and more.
  • Free ACMG Pathogenicity Calculator: A powerful tool to assess genetic variants based on ACMG/AMP guidelines.
  • Fast and Useful API: With a Pandas client for annotating variants in Python and a Java client for VCF file annotation.
  • Privacy-Focused Design: No third-party trackers, ensuring your data remains secure.

Key Features​

  • Evergreen Annotations: Continuously updated data from sources like GnomAD, ClinVar, Refseq, and more.
  • User-Friendly Interface: Simplifies navigation and exploration of genetic data.
  • API Access: Annotate VCF files, Pandas dataframes, or variant lists with ACMG scores, GnomAD frequencies, ClinVar annotations, and effect predictors. Learn more about our API.
  • Open-Source Tools: Check out our Python client on GitHub and our Java client for VCF annotation at genebe-cli.

Privacy and Security​

We take the privacy and security of our users' information seriously:

  • No Third-Party Tracking: We do not use Google Analytics or similar frameworks. All user queries and visited pages are private.
  • Secure Data Handling: We follow strict protocols to protect your data and do not sell or share personal information with third parties.
  • API Query Privacy: We do not store any queries made through our API, only counting the number of queries per day for fair resource usage. See our Rate Limits section for details.

Feedback​

As a beta platform, we value your input to improve GeneBe. Please share your ideas, suggestions, or concerns via our Feedback Form. Your feedback helps us enhance the platform and better serve the scientific community.

Learn More​

  • Explore our Variant Pathogenicity Calculator for detailed information on ACMG implementation.
  • Check the current and historic Website Status to ensure availability.
  • Visit GeneBe.net to start exploring genetic data today.

Thank you for choosing GeneBe. We hope you find our platform both useful and informative!