Achieve the highest diagnostic yield possible

 

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

Exomiser in the Congenica NGS data analysis platform helps improve 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

  • The only software for variant prioritization approved by IRDiRC