Evidence map›Paper›PMID 40826123›Full record

ArticleGenome medicine2025

Improving automated deep phenotyping through large language models using retrieval-augmented generation.

Brandon T Garcia, Lauren Westerfield, Priya Yelemali, Nikhita Gogate, E Andres Rivera-Munoz, Haowei Du, Moez Dawood, Angad Jolly, James R Lupski, Jennifer E Posey

Abstract read
In one paragraph

Article in Genome medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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  16. Domain specific phenotypic expansion associated with variants inmedRxiv : the preprint server for health sciences · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Brandon T GarciaDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Lauren WesterfieldDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Priya YelemaliDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Nikhita GogateDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
E Andres Rivera-MunozDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Haowei DuDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Moez DawoodDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Angad JollyDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
James R LupskiDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Jennifer E PoseyDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA. jep2156@cumc.columbia.edu.

Funding

Frequency of variants of unknown significance by ancestry groups in the All of Us Research Program cohortU01HG011758 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI RICHARD A GIBBS, JAMES R. LUPSKI · 2021 to 2026
$13.8M
NHGRI NIH HHS U01 HG011758
6 · The paper itself

Abstract

backgroundDiagnosing rare genetic disorders relies on precise phenotypic and genotypic analysis, with the Human Phenotype Ontology (HPO) providing a standardized language for capturing clinical phenotypes. Rule-based HPO extraction tools use concept recognition to automatically identify phenotypes, but they often struggle with incomplete phenotype assignment, requiring significant manual review. While large language models (LLMs) hold promise for more context-driven phenotype extraction, they are prone to errors and "hallucinations," making them less reliable without further refinement. We present RAG-HPO, a Python-based tool that leverages retrieval-augmented generation (RAG) to elevate accuracy of HPO term assignment by LLM. This approach bypasses the limitations of baseline models and eliminates the need for time- and resource-intensive fine-tuning. RAG-HPO integrates a dynamic vector database, containing > 54,000 phenotypic phrases mapped to HPO IDs, which allows real-time retrieval and contextual matching. The RAG-HPO workflow begins by extracting phenotypic phrases from clinical text via an LLM and then matching them via semantic similarity to entries within the database. The best term matches are returned to the LLM as context for final HPO term assignment of each phrase.

resultsPerformance was benchmarked on 112 published case reports with 1792 manually assigned HPO terms and compared to Doc2HPO, ClinPhen, and FastHPOCR. In evaluations, RAG-HPO + LLaMa-3.1 70B achieved a mean precision of 0.81, recall of 0.76, and an F1 score of 0.78-significantly surpassing conventional tools (p < 0.00001). RAG-HPO returned 1648 terms, of which 19.1% (315) were false positives that did not exactly match our manually annotated standard. Among these, < 1% (1/315) represented hallucinations, and 1.3% (4/315) represented terms with no ontological relationship to the desired target; the remaining false positives (95.2%, 300/315) were broader ancestor terms of the target term, which may still be relevant to users in many contexts.

conclusionsRAG-HPO is a user-friendly, adaptable tool designed for secure evaluation of clinical text and outperforms standard HPO-matching tools in precision, recall, and F1. Its enhanced precision and recall represent a substantial advancement in phenotypic analysis, accelerating the identification of genetic mechanisms underlying rare diseases and driving progress in genetic research and clinical genomics. RAG-HPO is available at https://github.com/PoseyPod/RAG-HPO .

Indexed as

PhenotypeBiological OntologiesHumansLanguageLarge Language ModelsSoftwareClinical genomicsGenerative AIGenerative pre-trained transformer (GPT)Human Phenotype Ontology (HPO)Large language models (LLMs)LLaMa-3Natural language processing (NLP)PhenotypingRetrieval-augmented generation (RAG)

Identifiers

PMID40826123
PMCPMC12359922

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.