A Brain Cell Type Resource Created by Large Language Models and a Multi-Agent AI System for Collaborative Community Annotation
- URL: http://arxiv.org/abs/2510.17064v2
- Date: Wed, 22 Oct 2025 03:31:51 GMT
- Title: A Brain Cell Type Resource Created by Large Language Models and a Multi-Agent AI System for Collaborative Community Annotation
- Authors: Rongbin Li, Wenbo Chen, Zhao Li, Rodrigo Munoz-Castaneda, Jinbo Li, Neha S. Maurya, Arnav Solanki, Huan He, Hanwen Xing, Meaghan Ramlakhan, Zachary Wise, Zhuhao Wu, Hua Xu, Michael Hawrylycz, W. Jim Zheng,
- Abstract summary: Single-cell RNA sequencing has transformed our ability to identify diverse cell types and their transcriptomic signatures.<n>Traditional methods, such as Gene Set Enrichment Analysis (GSEA), depend on well-curated annotations.<n>We present BRAINCELL-AID, a novel multi-agent AI system that integrates free-text descriptions with ontology labels.
- Score: 10.987335770634884
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Single-cell RNA sequencing has transformed our ability to identify diverse cell types and their transcriptomic signatures. However, annotating these signatures-especially those involving poorly characterized genes-remains a major challenge. Traditional methods, such as Gene Set Enrichment Analysis (GSEA), depend on well-curated annotations and often perform poorly in these contexts. Large Language Models (LLMs) offer a promising alternative but struggle to represent complex biological knowledge within structured ontologies. To address this, we present BRAINCELL-AID (BRAINCELL-AID: https://biodataai.uth.edu/BRAINCELL-AID), a novel multi-agent AI system that integrates free-text descriptions with ontology labels to enable more accurate and robust gene set annotation. By incorporating retrieval-augmented generation (RAG), we developed a robust agentic workflow that refines predictions using relevant PubMed literature, reducing hallucinations and enhancing interpretability. Using this workflow, we achieved correct annotations for 77% of mouse gene sets among their top predictions. Applying this approach, we annotated 5,322 brain cell clusters from the comprehensive mouse brain cell atlas generated by the BRAIN Initiative Cell Census Network, enabling novel insights into brain cell function by identifying region-specific gene co-expression patterns and inferring functional roles of gene ensembles. BRAINCELL-AID also identifies Basal Ganglia-related cell types with neurologically meaningful descriptions. Hence, we create a valuable resource to support community-driven cell type annotation.
Related papers
- GLaDiGAtor: Language-Model-Augmented Multi-Relation Graph Learning for Predicting Disease-Gene Associations [0.0]
Understanding disease-gene associations is essential to unravelling disease mechanisms and advancing diagnostics and therapeutics.<n>To address limitations in existing models, we propose GLaDiGAtor, a novel GNN framework with an encoder-decoder architecture for disease-gene association prediction.<n>GLaDiGAtor constructs a heterogeneous biological graph integrating gene-gene, disease-disease, and gene-disease interactions from curated databases.
arXiv Detail & Related papers (2026-02-21T09:26:44Z) - Contrastive Learning Enhances Language Model Based Cell Embeddings for Low-Sample Single Cell Transcriptomics [3.7907528918903797]
Large language models (LLMs) have shown ability in generating rich representations across domains such as natural language processing and generation, computer vision, and multimodal learning.<n>We present a computational framework that integrates single-cell RNA sequencing (scRNA-seq) with LLMs to derive knowledge-informed gene embeddings.
arXiv Detail & Related papers (2025-09-28T00:45:39Z) - Bridging Large Language Models and Single-Cell Transcriptomics in Dissecting Selective Motor Neuron Vulnerability [1.9638866836733835]
We generate biologically contextualized cell embeddings using gene-specific textual annotations from the NCBI Gene database.<n>For each cell in a single-cell RNA sequencing (scRNA-seq) dataset, we rank genes by expression level, retrieve their NCBI Gene descriptions, and transform these descriptions into vector embedding representations.
arXiv Detail & Related papers (2025-05-12T03:39:33Z) - GRAPE: Heterogeneous Graph Representation Learning for Genetic Perturbation with Coding and Non-Coding Biotype [51.58774936662233]
Building gene regulatory networks (GRN) is essential to understand and predict the effects of genetic perturbations.<n>In this work, we leverage pre-trained large language model and DNA sequence model to extract features from gene descriptions and DNA sequence data.<n>We introduce gene biotype information for the first time in genetic perturbation, simulating the distinct roles of genes with different biotypes in regulating cellular processes.
arXiv Detail & Related papers (2025-05-06T03:35:24Z) - GENERator: A Long-Context Generative Genomic Foundation Model [66.46537421135996]
We present GENERator, a generative genomic foundation model featuring a context length of 98k base pairs (bp) and 1.2B parameters.<n>Trained on an expansive dataset comprising 386B bp of DNA, the GENERator demonstrates state-of-the-art performance across both established and newly proposed benchmarks.<n>It also shows significant promise in sequence optimization, particularly through the prompt-responsive generation of enhancer sequences with specific activity profiles.
arXiv Detail & Related papers (2025-02-11T05:39:49Z) - scReader: Prompting Large Language Models to Interpret scRNA-seq Data [12.767105992391555]
We propose an innovative hybrid approach that integrates the general knowledge capabilities of large language models with domain-specific representation models for single-cell omics data interpretation.<n>By inputting single-cell gene-level expression data with prompts, we effectively model cellular representations based on the differential expression levels of genes across various species and cell types.
arXiv Detail & Related papers (2024-12-24T04:28:42Z) - VQDNA: Unleashing the Power of Vector Quantization for Multi-Species Genomic Sequence Modeling [60.91599380893732]
VQDNA is a general-purpose framework that renovates genome tokenization from the perspective of genome vocabulary learning.
By leveraging vector-quantized codebooks as learnable vocabulary, VQDNA can adaptively tokenize genomes into pattern-aware embeddings.
arXiv Detail & Related papers (2024-05-13T20:15:03Z) - Single-Cell Deep Clustering Method Assisted by Exogenous Gene
Information: A Novel Approach to Identifying Cell Types [50.55583697209676]
We develop an attention-enhanced graph autoencoder, which is designed to efficiently capture the topological features between cells.
During the clustering process, we integrated both sets of information and reconstructed the features of both cells and genes to generate a discriminative representation.
This research offers enhanced insights into the characteristics and distribution of cells, thereby laying the groundwork for early diagnosis and treatment of diseases.
arXiv Detail & Related papers (2023-11-28T09:14:55Z) - SemanticCAP: Chromatin Accessibility Prediction Enhanced by Features
Learning from a Language Model [3.0643865202019698]
We propose a new solution named SemanticCAP to identify accessible regions of the genome.
It introduces a gene language model which models the context of gene sequences, thus being able to provide an effective representation of gene sequences.
Compared with other systems under public benchmarks, our model proved to have better performance.
arXiv Detail & Related papers (2022-04-05T11:47:58Z) - Multi-modal Self-supervised Pre-training for Regulatory Genome Across
Cell Types [75.65676405302105]
We propose a simple yet effective approach for pre-training genome data in a multi-modal and self-supervised manner, which we call GeneBERT.
We pre-train our model on the ATAC-seq dataset with 17 million genome sequences.
arXiv Detail & Related papers (2021-10-11T12:48:44Z) - Select-ProtoNet: Learning to Select for Few-Shot Disease Subtype
Prediction [55.94378672172967]
We focus on few-shot disease subtype prediction problem, identifying subgroups of similar patients.
We introduce meta learning techniques to develop a new model, which can extract the common experience or knowledge from interrelated clinical tasks.
Our new model is built upon a carefully designed meta-learner, called Prototypical Network, that is a simple yet effective meta learning machine for few-shot image classification.
arXiv Detail & Related papers (2020-09-02T02:50:30Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.