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Babaiha, N. S.

Publications and source records attributed to Babaiha, N. S..

3 recordsLinked to original sources

Leveraging Multimodal Large Language Models to Extract Mechanistic Insights from Biomedical Visuals: A Case Study on COVID-19 and Neurodegenerative Diseases

BackgroundThe COVID-19 pandemic has intensified concerns about its long-term neurological impact, with growing evidence linking SARS-CoV-2 infection to neurodegenerative diseases (NDDs) such as Alzheimers (AD) and Parkinsons (PD). Patients with these conditions not only face higher risk of severe COVID-19 outcomes but may also undergo accelerated cognitive and motor decline following infection. Proposed mechanisms--ranging from neuroinflammation and blood-brain barrier disruption to abnormal protein aggregation--closely mirror core features of neurodegenerative pathology. Yet, current knowledge is fragmented across text, figures, and pathway diagrams, hindering integration into computational models capable of uncovering systemic patterns. ResultsTo address this gap, we applied GPT-4 Omni (GPT-4o), a multimodal large language model, to extract mechanistic insights from biomedical figures. Over 10,000 images were retrieved through targeted searches on COVID-19 and neurodegeneration; after automated and manual filtering, a curated subset was analyzed. GPT-4o extracted biological relationships as semantic triples, which were grouped into six mechanistic categories--including microglial activation and barrier disruption--using ontology-guided similarity and assembled into a Neo4j knowledge graph. Accuracy was evaluated against a gold-standard dataset of expert-annotated images using BioBERT-based semantic matching. This evaluation also enabled prompt tuning, threshold optimization, and hyperparameter assessment. Results demonstrate that GPT-4o successfully recovers both established and novel mechanisms, yielding interpretable outputs that illuminate complex biological links between SARS-CoV-2 and neurodegeneration. ConclusionsThis study showcases the potential of multimodal LLMs to mine biomedical visual data at scale. By complementing text mining and integrating figure-derived knowledge, our framework advances understanding of COVID-19-related neurodegeneration and supports future translational research.

bioinformatics↗

Unraveling the Co-Morbidity between COVID-19 and Neurodegenerative Diseases Through Multi-scale Graph Analysis: A Systematic Investigation of Biological Databases and Text Mining

The COVID-19 pandemic has generated a vast volume of research, yet much of it focuses on individual diseases, overlooking complex comorbidity relationships. While extensive literature exists on both neurodegenerative diseases (NDDs), such as Alzheimers and Parkinsons, and COVID-19, their intersection remains underexplored. Co-morbidity modeling is crucial, particularly for hospitalized patients often presenting with multiple conditions. This study investigates the interplay between COVID-19 and NDDs by integrating knowledge graphs (KGs) built from curated biomedical datasets and text mining tools. We performed comprehensive analyses--including path analysis, phenotype coverage, and mapping of cellular and genetic factors--across multiple KGs, such as PrimeKG, DrugBank, OpenTargets, and those generated via natural language processing (NLP) methods. Our findings reveal notable variability in graph density and connectivity, with each KG offering unique insights into molecular and phenotypic links between COVID-19 and NDDs. Key genetic and inflammatory markers, especially immune response genes, consistently appeared across graphs, suggesting a shared pathogenic basis. By unifying structured biological data with unstructured textual evidence, we enhance co-morbidity modeling and improve recall in identifying mechanisms underlying COVID-19- NDD interactions. This integrative framework supports the development of a co-morbidity hypothesis database aimed at facilitating therapeutic target discovery. All data, methods, and instructions for accessing the co-morbidity hypothesis database are publicly available at: https://github.com/SCAI-BIO/covid-NDD-comorbidity-NLP.

bioinformatics↗

NN-RNALoc: neural network-based model for prediction of mRNA sub-cellular localization using distance-based sub-sequence profiles

Localization of messenger RNAs (mRNA) as a widely observed phenomenon is considered as an efficient way to target proteins to a specific region of a cell and is also known as a strategy for gene regulation. The importance of correct intracellular RNA placement in the development of embryonic and neural dendrites has long been demonstrated in former studies. Improper localization of RNA in the cell, which has been shown to occur due to a variety of reasons, including mutations in trans-regulatory elements, is also associated with the occurrence of some neuromuscular diseases as well as cancer. We propose NN-RNALoc, a neural network-based model to predict the cellular location of mRNAs. The features extracted from mRNA sequences along with the information gathered from their proteins are fed to this prediction model. We introduce a novel distance-based sub-sequence profile for representation of RNA sequences which is more memory and time efficient and comparying to the k-mer frequencies, can possibly better encode sequences when the distance k increases. The performance of NN-RNALoc on the following benchmark datsets CeFra-seq and RNALocate, is compared to the results achieved by two powerful prediction models that were proposed in former studies named as mRNALoc and RNATracker The results reveal that the employment of protein-protein interaction information, which plays a crucial role in many biological functions, together with the novel distance-based sub-sequence profiles of mRNA sequences, leads to a more accurate prediction model. Besides, NN-RNALoc significantly reduces the required computing time compared to previous studies. Source code and data used in this study are available at: https://github.com/NeginBabaiha/NN-RNALoc

bioinformatics↗