Repository logo
  • English
  • 中文
Log In
Have you forgotten your password?
  1. Home
  2. College of Medicine / 醫學院
  3. National Taiwan University Hospital / 醫學院附設醫院 (臺大醫院)
  4. Genetic Diagnosis and Discovery Enabled by Large Language Models.
 
  • Details

Genetic Diagnosis and Discovery Enabled by Large Language Models.

Journal
Advanced science (Weinheim, Baden-Wurttemberg, Germany)
ISSN
2198-3844
Date Issued
2026-02-08
Author(s)
Tu, Tao
Saab, Khaled
Liu, Weida
Fang, Zhouqing
Cheng, Zhuanfen
Spasic, Svetolik
Djurisic, Maja
Mohri, Hiroaki
Ren, Wenlong
Palepu, Anil
Gottweis, Juraj
Karthikesalingam, Alan
Kulkarni, Kavita
Pawlosky, Annalisa
Bonner, Devon
Kravets, Elijah
Marwaha, Shruti
Mendez, Hector R
Wheeler, Matthew T
Bernstein, Jonathan A
Tsai, Cheng-Yu
CHEN-CHI WU  
Stankovic, Konstantina M
Natarajan, Vivek
Peltz, Gary
DOI
10.1002/advs.202518656
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/736860
Abstract
Artificial intelligence (AI) has been used in many areas of medicine, and large language models (LLMs) have shown potential utility for various clinical applications. However, to determine if LLMs can accelerate the pace of genetic diagnosis and discovery, we examined whether recently developed LLMs (Med-PaLM 2 and Gemini) could assist in solving four types of genetic problems with sequentially increasing complexity. First, in response to free-text input, Med-PaLM 2 correctly identified murine genes with experimentally verified causative genetic factors for six previously studied murine models of biomedical traits. Second, Med-PaLM 2 identified a novel causative murine genetic factor for spontaneous hearing loss that was validated using knock-in mice. Third, we developed a retrieval and grounding pipeline that enabled Gemini 2.5 Pro to analyze large lists of genes, which contained genetic variants that were identified in the genomic sequences of 20 human subjects with hearing loss, and demonstrated that it can assist in identifying causative genetic factors for hearing loss. Fourth, we modified the genetic analysis pipeline to enable Gemini 2.5 Pro without any task-specific fine-tuning to identify causative genetic factors for six subjects with rare genetic diseases, which required 14 to 34 different terms to describe their multi-faceted symptom complexes. These results demonstrate that an AI pipeline can facilitate genetic diagnosis and discovery in mice and humans.
Subjects
artificial intelligence
genetic discovery
large language model
Type
journal article

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

總館學科館員 (Main Library)
醫學圖書館學科館員 (Medical Library)
社會科學院辜振甫紀念圖書館學科館員 (Social Sciences Library)

開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

  • 請確認所上傳的全文是原創的內容,若該文件包含部分內容的版權非匯入者所有,或由第三方贊助與合作完成,請確認該版權所有者及第三方同意提供此授權。
    Please represent that the submission is your original work, and that you have the right to grant the rights to upload.
  • 若欲上傳已出版的全文電子檔,可使用Open policy finder網站查詢,以確認出版單位之版權政策。
    Please use Open policy finder to find a summary of permissions that are normally given as part of each publisher's copyright transfer agreement.
  • 網站簡介 (Quickstart Guide)
  • 使用手冊 (Instruction Manual)
  • 線上預約服務 (Booking Service)
  • 方案一:臺灣大學計算機中心帳號登入
    (With C&INC Email Account)
  • 方案二:ORCID帳號登入 (With ORCID)
  • 方案一:定期更新ORCID者,以ID匯入 (Search for identifier (ORCID))
  • 方案二:自行建檔 (Default mode Submission)
  • 方案三:學科館員協助匯入 (Email worklist to subject librarians)

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science