Carrier Screening for Inherited Disorders


Congenica software works with NGS data to enable screening of entire genes, in both the mother and the father, for the presence of disease-causing variants, eliminating the need to restrict analysis to a limited number of individual variants known to have an elevated carrier rate in a particular population. This approach gives a comprehensive picture of carrier risk and provides higher confidence for couples planning for a family – particularly in geographical areas with a dense population of individuals with shared ancestry.
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