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The leading system for human genome interpretation

  • Quickly get comprehensive disease annotations
  • Prioritize genes by pathogenic likelihood with VAAST
  • Get access to powerful genome comparison operations
  • Securely share results with colleagues
  • Get access to comprehensively annotated public genomes
  • Supports all sequencing platforms

Sign up now:

  • Complete this sign-up form
  • Review and accept the license agreement
  • Enter credit card information. You will not be charged now. You will only be charged when you upload data for annotation and analysis.
  • Activate your account by clicking on the link in the verification email

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