Maximize your diagnostic yield, efficiency &
confidence in the analysis of NGS data
- Accurately interpret genomic data in as little as 5-minutes
- Reduce interpretation costs and manual analysis by 95%
- Achieve the highest diagnostic yield possible
- Improve outcomes for patients
“Congenica enables us to analyze variants accurately, easily & quickly,
saving a lot of time in our NGS data and benefiting our patients.”
Dr Youngmok Lee, UConn Health, USA
“Congenica has been key in making our NGS interpretation services a success.”
Dr Gholson Lyon, M.D., Ph.D.
Institute for Basic Research in Developmental Disabilities, New York
