Evidence map›Paper›PMID 42555501›Full record

ArticleBriefings in bioinformatics2026

GeneGenie: enhancing biomedical question-answering with agentic graphs.

Mahmoud Gamal Abdelsalam, Abdulaziz H El-Safty, Amine Zaidi, Tanvir Alam

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2026. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Mahmoud Gamal AbdelsalamCollege of Science and Engineering, Hamad Bin Khalifa University, Doha, Qatar.ORCID 0009-0009-1129-7085
Abdulaziz H El-SaftyCollege of Science and Engineering, Hamad Bin Khalifa University, Doha, Qatar.ORCID 0000-0002-1504-6357
Amine ZaidiCollege of Science and Engineering, Hamad Bin Khalifa University, Doha, Qatar.
Tanvir AlamCollege of Science and Engineering, Hamad Bin Khalifa University, Doha, Qatar.ORCID 0000-0001-7033-3693

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large language models (LLMs) have revolutionized biomedical research, yet they remain prone to hallucinations and struggle with the precise, multi-hop reasoning required for biomedical analysis. To bridge this gap between generative capability of AI model and factual rigor, this article introduces GeneGenie, a model-agnostic, multi-agent framework built upon a directed acyclic graph architecture. Unlike static prompting strategies, GeneGenie implements a deterministic five-node pipeline that orchestrates query planning, intelligent retrieval-augmented generation across curated databases (GenCC, HGNC, and UniProt), and the dynamic execution of bioinformatics tools, including NCBI E-Utilities and local BLAST+. We evaluated the system using the updated 16-module GeneTuring benchmark, comprising 1600 question-answer pairs. The experimental design compared six state-of-the-art models-including GPT-4o, Claude Sonnet 4.5, and Gemini 2.5 Pro-operating in a standalone "Direct Mode" versus the agentic "Graph Mode." The results demonstrate that the graph-based architecture consistently outperforms single-model baselines across all metrics. Notably, among the six selected LLM models we explored, Gemini 2.5 Pro achieved the highest performance, correctly answering 1158 questions (72.375% accuracy), compared with the best baseline score of only 15.8%. Furthermore, our evaluation utilized an "LLM-as-Judge" semantic assessment, revealing that the agentic approach significantly enhances not only lexical accuracy but also the completeness and factual grounding of responses. While limitations remain in named entity recognition for protein-coding genes, GeneGenie establishes a robust, reproducible paradigm for future biomedical AI systems, proving that tool-augmented orchestration is superior to reliance on raw model scale alone.

Indexed as

Biomedical ResearchComputational BiologySoftwareAlgorithmsGenerative Artificial IntelligenceHumansLarge Language Modelsagentic graphbiomedical question answeringlarge language model (LLM)retrieval-augmented generation (RAG)

Identifiers

PMID42555501
PMCPMC13440129

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.