Spring 2026 Undergraduate Research Symposium
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B57: Automated Quantification of Whole Slide Steatosis Using a Custom LiverQuant Pipeline


Presenter(s)

Evan Mayse

Poster/exhibit session

11:45PM - 1:00PM: Poster session B

Faculty research mentor

David Alvarado

Authors

Daniel Alligood, MD, Xiuli Liu, MD PhD, Colin Martin, MD,

Abstract or Description

The histological gold standard for assessing hepatic steatosis relies on visual estimation by a trained pathologist, a process that is time-intensive and subject to observer variability. Automated image analysis offers opportunities to improve scalability, reproducibility, and throughput in liver disease research. This study evaluates a custom Python-based pipeline developed to implement and extend the LiverQuant framework in a murine model of intestinal failure-associated liver disease. Hematoxylin and eosin-stained whole-slide images were obtained from a longitudinal cohort of male and female mice undergoing sham operation or 75% small bowel resection, harvested at 2, 5, 10, and 26 weeks postoperatively, and scanned at 20x magnification using an Olympus VS120 whole-slide scanner. A total of 110 slides were analyzed. A custom pipeline was developed to convert whole-slide images, generate a tissue mask via color thresholding, and quantify steatosis as the percentage of lipid area relative to total tissue area. Automated measurements were compared with pathologist-derived estimates of steatosis using Pearson correlation analysis. Automated quantification demonstrated moderate-to-strong correlation with pathologist scoring across all time points (2wk: n=35, r=0.85; 5wk: n=29, r=0.78; 10wk: n=19, r=0.70; 26wk: n=27, r=0.67). Batch processing of 35 slides required approximately 39 minutes on a workstation and approximately one hour on a consumer-grade laptop. Pipeline performance was consistent across male and female cohorts. The custom LiverQuant-based pipeline provides an efficient and reproducible approach to whole-slide steatosis quantification with performance comparable to expert pathologist assessment, supporting its use as a scalable tool for experimental liver pathology research.

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