Hereditary Cancer Predisposition Services

Analyzing hereditary cancer requires precise identification of key variants and CNV’s as well as the right annotation resources to identify significant mutations. We offer a complete bioinformatic analysis solution to detect each type of variant: SNPs, Indels CNVs and mid-sized deletions. The platform also offers a number of tools to help categorize variants including annotation databases, automated ACMG scoring and a machine-learning-driven automatic variant ranking.