Genescreen is an advanced carrier screening test using NGS for full-exon analysis of genes associated with autosomal recessive and X-linked monogenic disorders. It detects pathogenic variants in asymptomatic individuals, providing an accurate reproductive risk assessment for severe genetic conditions.
With high sensitivity, GeneScreen detects both common and rare pathogenic variants, ensuring a comprehensive assessment of carrier status. Customisable panels for partner or donor-recipient matching can be expanded based on family history or clinical needs.
GeneScreen is indicated for individuals or couples with a genetic disease history, consanguinity, or those undergoing ART, gamete donation, or pregnancy.