Fine-tuning AI Foundation Models to Quantify Spatially-Resolved Cell-Type Fractions from Breast Cancer Digital Pathology Images
General data
| Credits (SWS) | 12 (10 SWS) |
| Module level | Master |
| Language | German/English |
| Total hours | 360 h |
| Weekly time slot | 2–3 days per week, with in-person attendance in Weihenstephan on Tuesdays |
| Block part in semester break | 03.08 - 14.08 or 21.09 - 02.10 |
Time schedule of the internship
| Apr 2026 | Kickoff meeting and assignment of projects and teams |
| Apr - Aug 2026 | Division of the project work, interim presentations |
| Aug - Oct 2026 | Blockpart for finalizing the project work, writing the report, and preparing the final presentation |
Requirements and prior knowledge
Bachelor's degree in Bioinformatics. Python and / or R skills. Prior skills in AI modeling (e.g. pytorch) and model tuning are a plus.
AI foundation models (e.g., Virchow, MUSK, OmniCLIP) offer tremendous potential for digital pathology and biomedicine by learning generalizable representations from large, heterogeneous datasets. These representations can be efficiently adapted to a wide range of tasks, enabling more accurate, scalable, and data-efficient analyses across molecular, cellular, and clinical domains. Critically, such models can be specialized for specific biomedical applications through fine-tuning on relatively small, task-specific datasets, which are far smaller than the massive datasets required for their original training.
This project aims to fine-tune AI foundation models to directly quantify spatially resolved cell-type abundances in breast cancer tumor tissues from standard, inexpensive H&E-stained histology images. By doing so, we can reduce dependence on complex and costly spatial transcriptomics experiments. Fine-tuning will leverage thousands of breast cancer H&E images paired with cell-type abundance estimates obtained from the deconvolution of matched spatial and/or bulk RNA-seq data, enabling the models to learn a direct mapping from histological images to the underlying cellular composition of the tumor microenvironment.
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