Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.09.11.675485

AIChatBio: An Artificial Intelligence Chatbot Model for Biological Knowledge Retrieval and Biomacromolecule Design

Abstract

Conversational agents for bioinformatics data analysis and interpretation remain largely inaccessible to the broader biological research community. This gap is especially pronounced in the current Generative AI era, which demands a paradigm shift in how researchers interact with computational tools. There is a pressing need to bridge well-established biological infrastructures and databases with the capabilities of Generative AI to democratize access to bioinformatics insights. In this study, we present an integrated framework that connects the robust bioinformatics resources of the National Center for Biotechnology Information (NCBI) with Generative AI through a novel Artificial Intelligence Chatbot Model for Biological Knowledge Retrieval and Biomacromolecule Design, AIChatBio. This operational model positions Generative AI as an intelligent information hub. User interactions with the chatbot are enriched by real-time data retrieval from web portal of the biological databases hosted at NCBI, which are then translated into structured inquiries toward the web applications of NCBI and bioinformatics analysis tools. These inquiries are directed toward bioinformatics analysis tools to perform tasks such as sequence alignment and primer design. Additionally, the outputs generated by these tools are interpreted by the chatbot, allowing users to gain meaningful insights without requiring deep technical expertise in bioinformatics. To demonstrate the feasibility of this approach, we developed a prototype implementation that integrates PCR primer design using Primer-BLAST [1], literature interpretation via PubMed for general topics, and the LitVar2 for SNPs associated topics [23]. This system was built using TypeScript and the ChatGPT API combining the bioinformatics web applications from NCBI, and its source code is publicly available via GitHub and the Chrome extension is available at Chrome Web Store. Our work highlights the potential of Generative AI to transform biological data analysis workflows, making them more intuitive, accessible, and scalable for researchers across disciplines.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Liu, E., Liu, C.-Y.. 2025-09-17. AIChatBio: An Artificial Intelligence Chatbot Model for Biological Knowledge Retrieval and Biomacromolecule Design. https://doi.org/10.1101/2025.09.11.675485

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

spatialMET: an open and scalable framework for spatial metabolomics analysis

Mass spectrometry imaging (MSI) enables spatially resolved metabolomics in intact tissue sections, but analysis remains challenging at scale. Existing MSI workflows often require users to combine multiple software tools, while others rely on proprietary vendor software that limits interoperability and reproducibility. To address these challenges, we developed spatialMET, an open-source framework that provides an end-to-end workflow for MSI analysis. spatialMET provides a unified platform for preprocessing, spatial domain detection, and visualization. Downstream analyses include differential abundance testing, spatial autocorrelation and gradient analysis, dimensionality reduction, and correlation network analysis. Spatial domain detection uses hcdist, a C-based hierarchical clustering implementation that substantially reduces runtime and memory use relative to existing R-based approaches. spatialMET can be run through an interactive R Shiny application or as a standalone command-line workflow for larger datasets or high-performance computing environments. Applied to mouse small cell lung cancer MALDI-MSI data containing 284,673 pixels, spatialMET identified tumor-associated, stromal, and adjacent lung spatial domains that aligned with matched histology. Differential abundance analysis identified 117 m/z features that differed between tumor and stromal regions, while spatial autocorrelation analyses revealed spatially structured abundance patterns. Applying spatialMET to mouse lung adenocarcinoma data from an entire lung lobe containing 338,477 pixels further demonstrated scalability and captured spatial heterogeneity across tumor and surrounding lung tissue. In summary, spatialMET provides a scalable, open-source framework for end-to-end spatial metabolomics analysis, and it is distributed as a Docker container for reproducible deployment. Source code and installation instructions are available at https://github.com/biodatalab/spatialMET.

bioinformatics↗

Probing the transcriptome response to shivering in skeletal muscle using a multilayered bioinformatics approach

Cold acclimation holds therapeutic potential for improving metabolic health. We previously demonstrated that repeated cold-induced shivering enhances insulin sensitivity in humans. However, the molecular pathways that underlie the skeletal muscle shivering response, and how these relate to beneficial physiological effects, remain poorly understood. In this study, we combined complementary bioinformatics approaches to allow in-depth analysis of the transcriptomic response of human skeletal muscle to repeated shivering. We identified a robust transcriptional signature and show a sex-specific component in the shivering skeletal muscle response, which seemed to diminish following cold adaptation. Our findings provide mechanistic insights into cold-induced muscle adaptations, shed light on potential interesting molecular targets for further investigation, and emphasize the importance of including both sexes in future cold acclimation studies.

bioinformatics↗

An Information Geometry approach to model topological trajectories and Gene Expression Radius from UMAP geometry.

Understanding the relationship between gene expression dynamics and cellular identity remains a central challenge in single cell biology. Here, we introduce a novel computational and mathematical framework that integrates information geometry, fuzzy topology, and UMAP analysis to model gene expression landscapes derived from single cell RNA sequencing data. We formalize gene expression data as a fuzzy topological space, where interactions between expression points are governed by probabilistic distributions inspired by manifold learning approaches such as UMAP. Within this framework, we define an information geometric structure through a Fisher metric induced by these distributions, enabling the computation of geodesic trajectories that capture cellular differentiation processes. A key contribution of this work is the derivation of analytical conditions, expressed as expression radius formulas, that characterize local neighborhoods in gene expression space. These conditions allow for the identification of genes associated with stem cell states and predictions in transitional cell types in future work. Application of the proposed framework to single cell datasets reveals biologically meaningful gene sets enriched in key regulatory pathways and transcription factors, demonstrating the capacity of our approach to uncover latent structure in complex gene expression data. Our results suggest that integrating differential geometry with statistical learning theory offers a powerful paradigm for modeling genotype and phenotype relationships and cellular state transitions, with potential implications for precision medicine and systems biology.

bioinformatics↗