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
