Achieve the highest diagnostic yield possible

Manually identifying causative variants takes time and limits diagnostic yield, meaning fewer cases can be solved.

Exomiser sits at the heart of the Congenica NGS data analysis platform and improves diagnostic yields by an average of 30%.


Key benefits:

  • Causal variants ranked 1st more than in any other tool

  • Automate variant prioritization in all sample types from genomes to panels

  • Complete whole genome variant prioritization in under 5-minutes


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