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Utilization of AI for Paper Search in the Exploration of New Targets for Pompe Disease in the Rare Disease Analysis Series

FRONTEO

【Event Overview】 In the Rare Disease Analysis Series, we will introduce the system overview and utilization methods of the paper exploration AI system "KIBIT Amanogawa," which can instantly detect papers, genes, and diseases that are highly similar or relevant to the words or sentences entered from a vast amount of paper information, focusing on the theme of target exploration for rare diseases. The theme for this session is "Pompe Disease." Pompe disease is one of the types of glycogen storage disease (GSD), specifically GSD type 2, caused by a deficiency of acid alpha-glucosidase. It presents symptoms such as muscle weakness and cardiomyopathy, and when it occurs in infancy, it can lead to very severe symptoms. In this seminar, we will demonstrate how to extract genes related to Pompe disease using paper exploration AI and formulate hypotheses for therapeutic targets, providing effective ways to utilize KIBIT Amanogawa to gain insights for research. 【Participation Conditions】 We kindly ask that individuals using free addresses, those from competing companies, and those whose affiliations are unclear refrain from applying. When accessing Zoom on the day of the event, please enter the name and email address you provided at the time of registration in the Zoom participation input field.