A systematic review on the generative AI applications in human medical genetics

Although traditional statistical techniques and machine learning methods have contributed significantly to genetics and, in particular, inherited disease diagnosis, they often struggle with complex, high-dimensional data, a challenge now addressed by state-of-the-art deep learning models. Large language models (LLMs), based on transformer architectures, have excelled in tasks requiring contextual comprehension of unstructured medical data. This systematic review examines the role of generative Artificial Intelligence (AI) methods in human medical genomics, focusing on the genetic research and diagnostics of both rare and common diseases. Automated keyword-based search in PubMed, bioRxiv, medRxiv, and arXiv was conducted, targeting studies on LLM applications in diagnostics and education within genetics and removing irrelevant or outdated models. A total of 195 studies were analyzed, highlighting the prospects of their applications in knowledge navigation, analysis of clinical and genetic data, and interaction with patients and medical professionals. Key findings indicate that while transformer-based models perform well across a diverse range of tasks (such as identification of tentative molecular diagnosis from clinical data or genetic variant interpretation), major challenges persist in integrating multimodal data (genomic sequences, imaging, and clinical records) into unified and clinically robust pipelines, facing limitations in generalizability and practical implementation in clinical settings. This review provides a comprehensive classification and assessment of the current capabilities and limitations of LLMs in transforming hereditary disease diagnostics and supporting genetic education, serving as a guide to navigate this rapidly evolving field, while outlining application use cases, implementation guidance, and forward-looking research directions.

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Publication Details

Journal
Frontiers in Genetics
Published
2026-01-20
DOI
https://doi.org/10.3389/fgene.2025.1694070
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

A systematic review on the generative AI applications in human medical genetics

Anton I. Changalidis, Yury A. Barbitoff, Yulia A. Nasykhova, Andrey Sergeevich Glotov
Frontiers in Genetics
Genomics and Rare Diseases
article

A systematic review on the generative AI applications in human medical genetics

Anton I. Changalidis, Yury A. Barbitoff, Yulia A. Nasykhova, Andrey Sergeevich Glotov
article en

Abstract

Although traditional statistical techniques and machine learning methods have contributed significantly to genetics and, in particular, inherited disease diagnosis, they often struggle with complex, high-dimensional data, a challenge now addressed by state-of-the-art deep learning models. Large language models (LLMs), based on transformer architectures, have excelled in tasks requiring contextual comprehension of unstructured medical data. This systematic review examines the role of generative Artificial Intelligence (AI) methods in human medical genomics, focusing on the genetic research and diagnostics of both rare and common diseases. Automated keyword-based search in PubMed, bioRxiv, medRxiv, and arXiv was conducted, targeting studies on LLM applications in diagnostics and education within genetics and removing irrelevant or outdated models. A total of 195 studies were analyzed, highlighting the prospects of their applications in knowledge navigation, analysis of clinical and genetic data, and interaction with patients and medical professionals. Key findings indicate that while transformer-based models perform well across a diverse range of tasks (such as identification of tentative molecular diagnosis from clinical data or genetic variant interpretation), major challenges persist in integrating multimodal data (genomic sequences, imaging, and clinical records) into unified and clinically robust pipelines, facing limitations in generalizability and practical implementation in clinical settings. This review provides a comprehensive classification and assessment of the current capabilities and limitations of LLMs in transforming hereditary disease diagnostics and supporting genetic education, serving as a guide to navigate this rapidly evolving field, while outlining application use cases, implementation guidance, and forward-looking research directions.

Frontiers in GeneticsVol. 16
Research Institute of Obstetrics and Gynecology named after D.O. Ott (RU)
Ministry of Science and Higher Education of the Russian Federation
Quality Education
Openalex Percentile: Top 84%
Genomics and Rare Diseases
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