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Butler, K. S.

Publications and source records attributed to Butler, K. S..

2 recordsLinked to original sources

Benchmarking Large Language Models for Transcriptomic Data Analysis and Visualization: Multi-Model Workflow Evaluation

This study presents a comprehensive benchmarking evaluation of large language models(LLMs) and agentic coding systems for automated analysis and visualization workflows for transcriptomic data, in particular human responses to COVID-19 infection. Multiple models, including ChatGPT 5.5, Claude Sonnet 4.6, Gemini 3.1, and Llama4-Scout, were assessed across a series of scientific prompts designed to test their ability to reproduce workflow components such as dimensionality reduction, clustering, outlier detection, reproducibility, and code generation. The benchmark protocol involved varying prompt specificity and examined both quantitative metrics such as clustering scores and outlier counts as well as qualitative aspects such as code quality and reproducibility. Results indicate that prompt specificity improves code structure and methodological correctness, but quantitative performance depends heavily on preprocessing choices and execution environment. While some models produced strong code and reproducible outputs, alignment with scientific targets like label-based clustering was inconsistent. The findings highlight the promise and limitations of current LLMs for automating scientific data analysis and visualization and suggest directions for future benchmarking and workflow standardization.

bioinformatics↗

Augmentation of Antibacterial Activity in Mesenchymal Stromal Cells Through Systems-Level Analysis and CRISPR-mediated Activation of CD14

Mesenchymal stromal cells (MSCs) have broad-ranging therapeutic capabilities, however MSC use is confounded by cell-to-cell heterogeneity, and source-to-source phenotypic inconsistencies. We utilized a systems-based approach to compare MSCs which displayed different capacity for antibacterial activity. Although MSCs from both sources satisfied traditional MSC-defining criteria, comparative transcriptomics and quantitative membrane proteomics demonstrated two unique molecular profiles. The antibacterial MSCs respond rapidly to bacterial lipopolysaccharide (LPS) and have elevated levels of the LPS co-receptor CD14. CRISPR-mediated overexpression of endogenous CD14 in non-antibacterial MSCs resulted in faster LPS response and enhanced antimicrobial activity. Single-cell transcriptome profiling of CD14-activated MSCs revealed uniform enhancement of LPS response kinetics, and a shift in the ground state of these MSCs. Our results demonstrate that systems-level analysis can reveal critical molecular targets to optimize desirable properties in MSCs, and that overexpression of CD14 in these cells can shift their state to be more responsive to future bacterial challenge.

molecular biology↗