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.
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The VKB (Variant Knowledge Base) facilitates the sharing of variant information within your team as well as providing the option to import your own annotation databases.
NOTE: Privacy is of key importance. VKB data is never shared outside of your organization.
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