The increasing volume of genomic literature presents significant challenges in the efficient retrieval and synthesis of genomic variant-specific information, which is critical for clinical and research applications. To address these challenges, we introduce VarChat, a novel generative AI-based platform designed to optimize the retrieval and summarization of up-to-date literature directly citing genomic variants of interest. VarChat uses different literature databases within a hybrid RAG framework that integrates both sparse and dense retrieval approaches and synthesizes these fragmented literature findings into concise, scientifically rigorous summaries while providing direct access to high-confidence references. The platform also integrates a guided chat feature, enabling users to explore specific questions related to the functional and clinical implications of genomic variants. VarChat integrates literature preprocessing and advanced hybrid retrieval techniques to accelerate the genomic variant interpretation process, supporting the genomic community in improving clinical decision. Availability: VarChat is freely available at varchat.engenome.com.

Generative AI Meets Genomics: VarChat, a RAG-Based Approach for Literature-Driven Variant Summarization

De Paoli F.;Berardelli S.;Tudisco A.;Blindu A.;Parimbelli E.;Zucca S.
2025-01-01

Abstract

The increasing volume of genomic literature presents significant challenges in the efficient retrieval and synthesis of genomic variant-specific information, which is critical for clinical and research applications. To address these challenges, we introduce VarChat, a novel generative AI-based platform designed to optimize the retrieval and summarization of up-to-date literature directly citing genomic variants of interest. VarChat uses different literature databases within a hybrid RAG framework that integrates both sparse and dense retrieval approaches and synthesizes these fragmented literature findings into concise, scientifically rigorous summaries while providing direct access to high-confidence references. The platform also integrates a guided chat feature, enabling users to explore specific questions related to the functional and clinical implications of genomic variants. VarChat integrates literature preprocessing and advanced hybrid retrieval techniques to accelerate the genomic variant interpretation process, supporting the genomic community in improving clinical decision. Availability: VarChat is freely available at varchat.engenome.com.
2025
Lecture Notes in Computer Science
Inglese
23rd International Conference on Artificial Intelligence in Medicine, AIME 2025
2025
ita
15735
127
131
5
9783031958403
9783031958410
Springer Science and Business Media Deutschland GmbH
Generative AI; Genomic Variant Interpretation; Literature Retrieval
no
none
De Paoli, F.; Berardelli, S.; Tudisco, A.; Blindu, A.; Parimbelli, E.; Zucca, S.
273
info:eu-repo/semantics/conferenceObject
6
4 Contributo in Atti di Convegno (Proceeding)::4.1 Contributo in Atti di convegno
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1549983
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