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
HubSpot Video

“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