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Discover how our solution leads to more interesting findings in your research.

  • Leverage trusted content of HGMD in combination with unique literature-curated zygosity and ethnicity information to ensure that no published mutation is overlooked or misinterpreted
  •  Use your knowledge of an individual’s symptoms to create causal variant hypotheses that extend beyond known gene-disease associations by mining vast networks of linked pathway relationships
  •  Multiply the answers in your search for causal variants via direct opt-in to the Allele Frequency Community, or mine QIAGEN Inova Genomes; a disease reference and control data set of 7,000+ whole genomes, to identify and validate potential causal variants