Open-source framework for detecting bias and overfitting for large pathology images

Sildnes, Anders, Shvetsov, Nikita, Tafavvoghi, Masoud, Tran, Vi Ngoc-Nha, Møllersen, Kajsa, Busund, Lill-Tove Rasmussen, Kilvær, Thomas K., Bongo, Lars Ailo

arXiv.org Artificial Intelligence 

Abstract--Even foundational models that are trained on datasets with billions of data samples may develop shortcuts that lead to overfitting and bias. Shortcuts are non-relevant patterns in data, such as the background color or color intensity. So, to ensure the robustness of deep learning applications, there is a need for methods to detect and remove such shortcuts. Today's model debugging methods are time consuming since they often require customization to fit for a given model architecture in a specific domain. We propose a generalized, model-agnostic framework to debug deep learning models. We focus on the domain of histopathology, which has very large images that require large models - and therefore large computation resources. It can be run on a workstation with a commodity GPU. We demonstrate that our framework can replicate non-image shortcuts that have been found in previous work for self-supervised learning models, and we also identify possible shortcuts in a foundation model. Our easy to use tests contribute to the development of more reliable, accurate, and generalizable models for WSI analysis. Pathologists examining tissue specimens mounted on glass slides using a high-powered microscope is the gold standard for cancer diagnosis. Currently, glass slides are digitized into whole-slide images (WSI) that comprise billions of pixels and millions of cells. However, it is difficult for humans to extract all relevant features for prognosis in the plethora of information available in a WSI. Deep learning (DL) models therefore show great promise for WSI analysis both by themselves and as decision support for pathologists. For example, DL has demonstrated its usefulness for cancer type classification [3][9], tissue segmentation [19] and analysis of tissue microenvironments [39][41].

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