Evidence map›Paper›PMID 41148224›Full record

ArticleBriefings in bioinformatics2025

BrainGeneBot: a framework for variant prioritization and generative pretrained transformer-informed interpretation across polygenic risk score studies.

Gang Qu, Nitesh Enduru, Xinyi Liu, Xiaoqian Jiang, Zhongming Zhao

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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

5 authors.

Gang QuCenter for Precision Health, McWilliams School of Biomedical Informatics, The University of Texas Health Science Center at Houston 7000 Fannin Street, Suite 600, Texas Medical Center, Houston, Harris County, TX 77030, United States.ORCID 0000-0003-2681-0880
Nitesh EnduruCenter for Precision Health, McWilliams School of Biomedical Informatics, The University of Texas Health Science Center at Houston 7000 Fannin Street, Suite 600, Texas Medical Center, Houston, Harris County, TX 77030, United States.ORCID 0000-0002-0255-706X
Xinyi LiuCenter for Precision Health, McWilliams School of Biomedical Informatics, The University of Texas Health Science Center at Houston 7000 Fannin Street, Suite 600, Texas Medical Center, Houston, Harris County, TX 77030, United States.ORCID 0000-0001-6862-1004
Xiaoqian JiangDepartment of Health Data Science and Artificial Intelligence, McWilliams School of Biomedical Informatics, The University of Texas Health Science Center at Houston 7000 Fannin Street, Suite 600, Texas Medical Center, Houston, Harris County, TX 77030, United States.ORCID 0000-0001-9933-2205
Zhongming ZhaoCenter for Precision Health, McWilliams School of Biomedical Informatics, The University of Texas Health Science Center at Houston 7000 Fannin Street, Suite 600, Texas Medical Center, Houston, Harris County, TX 77030, United States.ORCID 0000-0002-3477-0914

Funding

AIM-AI: an Actionable, Integrated and Multiscale genetic map of Alzheimer's disease via deep learningU01AG079847 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Christopher A. Gaiteri, Xiaoqian Jiang · 2023 to 2026
$5.1M
Transforming dbGaP genetic and genomic data to FAIR-ready by artificial intelligence and machine learning algorithmsR01LM012806 · NLM · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Zhongming Zhao · 2017 to 2026
$3.7M
Deep learning for decoding genetic regulation and cellular maps in craniofacial developmentR01DE030122 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI IWATA, JUNICHI, ZHAO, ZHONGMING · 2021 to 2023
$1.7M
Biomedical Informatics, Genomics and Translational Cancer Research Training ProgramCancer Prevention and Research Institute of Texas CPRIT RP210045CPRIT Postdoctoral FellowshipNIA NIH HHS U01 AG079847NIDCR NIH HHS R01 DE030122NIH HHS R01DE030122NIH HHS R01LM012806NIH HHS R01LM012806-07S1NIH HHS U01AG079847NLM NIH HHS R01 LM012806UTHealth Cancer Genomics Core for technical RP240610
6 · The paper itself

Abstract

Polygenic risk scores (PRS) are widely used to assess genetic susceptibility in Alzheimer's disease (AD) research. However, the rapid expansion of PRS studies has led to dataset-specific biases-stemming from factors like population makeup, genotyping methods, and analysis pipelines-that result in inconsistent variant prioritization and limit generalizability and reproducibility. To address these challenges, we propose a transductive learning framework that integrates multiple PRS datasets for more robust risk variant prioritization, incorporating genome-wide association study (GWAS) priority scores as biologically informed priors. Additionally, we introduce BrainGeneBot, an AI-driven tool leveraging generative pretrained transformers with retrieval-augmented generation technology to streamline genomic analyses in AD, including the STRING for protein interaction analysis, Enrichr for gene set enrichment, ClinVar for genetic variant interpretation, and Biopython for conducting literature searches. We apply our approach to publicly available AD datasets from the PGS Catalog and conduct further analyses to validate its efficacy. In parallel, we perform conventional unsupervised rank aggregation as a baseline. The transductive learning approach not only verifies high-risk variants identified by traditional methods but also reveals unique insights that better correlate with GWAS signals. Our framework streamlines data retrieval and interpretation, effectively prioritizing genetic variants in multiple PRS studies. Moreover, BrainGeneBot facilitates the discovery of biologically meaningful insights to enhance PRS interpretability and applicability in AD research, supporting the development of precise AD interventions and treatments. Our approach provides a robust framework for AD genetic research, improving data accessibility, accelerating discoveries, and refining genetic insights.

Indexed as

Alzheimer DiseaseGenetic Predisposition to DiseaseGenome-Wide Association StudyMultifactorial InheritanceSoftwareGenetic Risk ScoreHumansPolymorphism, Single Nucleotidegenomic analysisGPT-powered informaticspolygenic scorerank aggregationtransductive learning

Identifiers

PMID41148224
PMCPMC12560794

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LicenceCC BY-NC
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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.