IVCVNov 24, 2024

Comparative Analysis of Diffusion Generative Models in Computational Pathology

arXiv:2411.15719v11 citationsh-index: 26Has Code
Originality Synthesis-oriented
AI Analysis

This work addresses the need for improved synthetic data generation in computational pathology, though it appears incremental as it applies existing methods to a new domain.

The paper tackled the application of diffusion generative models to computational pathology by conducting a comparative analysis on pathology datasets, finding that these models effectively produce high-quality synthetic data and that adjusting image size can simulate varying fields of view.

Diffusion Generative Models (DGM) have rapidly surfaced as emerging topics in the field of computer vision, garnering significant interest across a wide array of deep learning applications. Despite their high computational demand, these models are extensively utilized for their superior sample quality and robust mode coverage. While research in diffusion generative models is advancing, exploration within the domain of computational pathology and its large-scale datasets has been comparatively gradual. Bridging the gap between the high-quality generation capabilities of Diffusion Generative Models and the intricate nature of pathology data, this paper presents an in-depth comparative analysis of diffusion methods applied to a pathology dataset. Our analysis extends to datasets with varying Fields of View (FOV), revealing that DGMs are highly effective in producing high-quality synthetic data. An ablative study is also conducted, followed by a detailed discussion on the impact of various methods on the synthesized histopathology images. One striking observation from our experiments is how the adjustment of image size during data generation can simulate varying fields of view. These findings underscore the potential of DGMs to enhance the quality and diversity of synthetic pathology data, especially when used with real data, ultimately increasing accuracy of deep learning models in histopathology. Code is available from https://github.com/AtlasAnalyticsLab/Diffusion4Path

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