Biology subjects

Bansal, B.

Publications and source records attributed to Bansal, B..

3 recordsLinked to original sources

bioRxiv2026

Ignet 2.0 and Vignet: An Ontology-Driven Web Platform for Biomedical Gene Interaction Discovery and Visualization

BackgroundThe expansion of biomedical literature demands systematic ontology-guided discovery of gene interactions, vaccine mechanisms, drug associations, and adverse events. Existing platforms such as STRING, DisGeNET, and PubTator fall short of providing a unified, freely accessible system that integrates ontology-based semantic interaction classification, vaccine-focused heterogeneous network construction, and Artificial Intelligence-assisted evidence retrieval. ResultsIgnet 2.0 and Vignet are freely accessible dual-platform systems that combine PubMed literature mining, BioBERT-based interaction scoring for millions of gene-gene co-occurrence pairs and integrate three biomedical ontologies and one curated drug resource, Interaction Network Ontology (INO), Vaccine Ontology (VO), Human Disease Ontology (HDO), and DrugBank. Ignet 2.0 supports gene interaction discovery, gene set enrichment retrieval of BioBERT-scored GenePair evidence, and AI-assisted summarization through BioSummarAI. Vignet extends these features with VO-guided Vaccine Exploration, VacPair interaction scoring, and the creation of vaccine, gene, drug, and disease networks in VacNet. A public Representational State Transfer Application Programming Interface (REST API) and Model Context Protocol (MCP) endpoint enable real-time integration, fostering trust in biomedical knowledge discovery. ConclusionIgnet 2.0 and Vignet are scalable, ontology-guided biomedical knowledge platforms that facilitate evidence-based gene interaction analysis, vaccine-focused semantic exploration, and AI-assisted knowledge discovery. Their real-time PubMed data integration ensures up-to-date insights; however, users should consider validation processes and potential lags in incorporating the latest experimental data, which may affect the reliability of immediate data. AvailabilityIgnet 2.0: https://ignet.org/ignet; Vignet: https://ignet.org/vignet/

bioinformatics↗

bioRxiv2025

VO: The Vaccine Ontology

With the widespread use of vaccines in research and clinical settings, there is an urgent need to standardize vaccine representation, integrate information across diverse vaccine types, and support computer-assisted reasoning. Accordingly, we have since 2007 developed the community-based Vaccine Ontology (VO), which aligns with the Basic Formal Ontology and adheres to OBO Foundry principles. VO models ontologically vaccines, vaccine components, vaccine immune responses, vaccine investigation studies and other vaccine-related topics. VO represents more than 10,000 vaccines targeting 289 infectious pathogens and cancers in humans and over 30 nonhuman animal species. VO provides mappings to external resources such as RxNorm, CVX, FDA, and USDA. Various VO use cases exist. VO facilitates vaccine standardization in resources such as the VIOLIN vaccine database, ImmPort, and the Vaccine Adjuvant Compendium (VAC). Semantic queries can be made to query VO. VO has been shown to enhance experimental and clinical vaccine data analysis and vaccine literature mining. Overall, VO standardizes vaccine modeling and representation and greatly supports vaccine AI research in the Semantic Web era.

bioinformatics↗

bioRxiv2025

Ontology-based Protein-Protein Interaction Explanation Using Large Language Models

Protein-protein interactions (PPIs) play a crucial role in various biological processes, and understanding these interactions is essential for advancing biomedical research. Automated extraction and analysis of PPI information from the rapidly growing scientific literature remains an important challenge. We present a novel ontology-based approach to analyze protein-protein interactions using Large Language Models (LLMs). We applied different learning strategies, namely in-context learning and parameter-efficient instruction fine-tuning for the Llama-2 chat models, to identify keywords in the text that indicate an interaction between a pair of proteins. Our results show that parameter-efficient fine-tuning leads to a performance gain even when the domain is new. The smaller fine-tuned models outperformed the zero-shot performance of much larger models. The keywords identified by the Llama-2 models were mapped to the ontology terms in the Interaction Network Ontology (INO). Our study suggests that a pipeline of an LLM and an ontology is an effective strategy for explaining relations between biomedical entities. This work demonstrates the potential of leveraging ontologies and advanced language models to advance automated PPI analysis from the scientific literature.

bioinformatics↗