Evidence map›Paper›PMID 42369077›Full record

ArticleProceedings. IEEE International Conference on Bioinformatics and Biomedicine2025

A Knowledge-Guided Large Language Model Framework for Microbiome-Based Disease Diagnosis.

Chengyuan Liu, Huiye Han, Youran Qi, Wodan Ling

Abstract read
In one paragraph

Article in Proceedings. IEEE International Conference on Bioinformatics and Biomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Chengyuan LiuPopulation Health Sciences, Weill Cornell Medicine, New York, USA.
Huiye HanPopulation Health Sciences, Weill Cornell Medicine New York, USA.
Youran QiIndependent Researcher, New York, USA.
Wodan LingPopulation Health Sciences, Weill Cornell Medicine, New York, USA.

Funding

Statistical Methods for Enhanced Mapping of Microbiome RelationshipsR01GM151301 · NIGMS · FRED HUTCHINSON CANCER CENTER · PI MICHAEL Chiao-An WU · 2023 to 2026
$1.2M
Robust Statistical Methods for Longitudinal Microbiome StudiesR01GM155734 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI Wodan Ling · 2024 to 2026
$1.2M
NIGMS NIH HHS R01 GM151301NIGMS NIH HHS R01 GM155734
6 · The paper itself

Abstract

Gut microbiome-based disease diagnosis holds significant promise but remains challenging due to the high data dimensionality, typically small sample sizes, and the necessity of incorporating biological knowledge. Due to these challenges, traditional machine learning approaches often tend to overfit the data and fail to capture true biological relationships, resulting in inaccurate diagnoses. To fill in the gap, we propose a two-phase, knowledge-guided large language model (LLM) framework for disease diagnosis that integrates biomedical expertise with in-context learning. In Phase 1, an LLM is employed to identify disease-associated taxa from hundreds of microbial families and to infer their biological relationships with the disease outcome. This process reduces the feature space dimensionality through biologically-informed feature selection and acquires essential domain knowledge. In Phase 2, we employ few-shot prompting to guide the LLM in disease outcome classification based on the domain knowledge acquired in Phase 1. Thanks to the universal applicability of LLM and our two-phase approach, this is a generic framework that can be applied to a wide range of microbiome-based disease diagnostic tasks. We demonstrate the superiority of our framework using inflammatory bowel disease (IBD) as a representative case study, where our approach achieves an accuracy of 73.91%, significantly outperforming an optimized XGBoost classifier. Overall, our knowledge-guided framework provides a powerful and generalizable strategy for leveraging LLMs in microbiome-based disease diagnosis, and opens a new avenue for disease diagnosis in the era of LLM.

Indexed as

Disease diagnosisIn-context learningInflammatory bowel diseaseLarge language modelsMicrobiome

Identifiers

PMID42369077
PMCPMC13309222

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.