Kath is a user-friendly GUI tool designed to streamline the in-depth analysis of gene variation data from LOVD, gnomAD and ClinVar genetic databases. By consolidating critical information into an accessible interface, Kath empowers researchers, clinicians and geneticists to uncover actionable insights with ease.
Built for efficiency and adaptability, it is ideal for tasks such as assessing pathogenicity or cross-referencing genetic variant data. It serves as a vital tool for advancing research, improving diagnostics and supporting genomic studies.
We are honored to recognize the contributions of our advisors who bring expertise, resources and guidance to the development of Kath. Their support is instrumental in ensuring the quality, innovation and impact of our tool in the field of genetics.
