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Frederick Klauschen

Possible papers associated with this exact author name in Arrow. This page groups case-insensitive exact name matches and is not a full identity disambiguation profile.

3 papers
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3

TMLR Journal 2025 Journal Article

Explaining Bayesian Neural Networks

  • Kirill Bykov
  • Marina MC Höhne
  • Adelaida Creosteanu
  • Klaus Robert Muller
  • Frederick Klauschen
  • Shinichi Nakajima
  • Marius Kloft

To advance the transparency of learning machines such as Deep Neural Networks (DNNs), the field of Explainable AI (XAI) was established to provide interpretations of DNNs' predictions. While different explanation techniques exist, a popular approach is given in the form of attribution maps, which illustrate, given a particular data point, the relevant patterns the model has used for making its prediction. Although Bayesian models such as Bayesian Neural Networks (BNNs) have a limited form of transparency built-in through their prior weight distribution, they lack explanations of their predictions for given instances. In this work, we take a step toward combining these two perspectives by examining how local attributions can be extended to BNNs. Within the Bayesian framework, network weights follow a probability distribution; hence, the standard point explanation extends naturally to an explanation distribution. Viewing explanations probabilistically, we aggregate and analyze multiple local attributions drawn from an approximate posterior to explore variability in explanation patterns. The diversity of explanations offers a way to further explore how predictive rationales may vary across posterior samples. Quantitative and qualitative experiments on toy and benchmark data, as well as on a real-world pathology dataset, illustrate that our framework enriches standard explanations with uncertainty information and may support the visualization of explanation stability.

NeurIPS Conference 2024 Conference Paper

xMIL: Insightful Explanations for Multiple Instance Learning in Histopathology

  • Julius Hense
  • Mina Jamshidi Idaji
  • Oliver Eberle
  • Thomas Schnake
  • Jonas Dippel
  • Laure Ciernik
  • Oliver Buchstab
  • Andreas Mock

Multiple instance learning (MIL) is an effective and widely used approach for weakly supervised machine learning. In histopathology, MIL models have achieved remarkable success in tasks like tumor detection, biomarker prediction, and outcome prognostication. However, MIL explanation methods are still lagging behind, as they are limited to small bag sizes or disregard instance interactions. We revisit MIL through the lens of explainable AI (XAI) and introduce xMIL, a refined framework with more general assumptions. We demonstrate how to obtain improved MIL explanations using layer-wise relevance propagation (LRP) and conduct extensive evaluation experiments on three toy settings and four real-world histopathology datasets. Our approach consistently outperforms previous explanation attempts with particularly improved faithfulness scores on challenging biomarker prediction tasks. Finally, we showcase how xMIL explanations enable pathologists to extract insights from MIL models, representing a significant advance for knowledge discovery and model debugging in digital histopathology.

NeurIPS Conference 2023 Conference Paper

DiffInfinite: Large Mask-Image Synthesis via Parallel Random Patch Diffusion in Histopathology

  • Marco Aversa
  • Gabriel Nobis
  • Miriam Hägele
  • Kai Standvoss
  • Mihaela Chirica
  • Roderick Murray-Smith
  • Ahmed M. Alaa
  • Lukas Ruff

We present DiffInfinite, a hierarchical diffusion model that generates arbitrarily large histological images while preserving long-range correlation structural information. Our approach first generates synthetic segmentation masks, subsequently used as conditions for the high-fidelity generative diffusion process. The proposed sampling method can be scaled up to any desired image size while only requiring small patches for fast training. Moreover, it can be parallelized more efficiently than previous large-content generation methods while avoiding tiling artifacts. The training leverages classifier-free guidance to augment a small, sparsely annotated dataset with unlabelled data. Our method alleviates unique challenges in histopathological imaging practice: large-scale information, costly manual annotation, and protective data handling. The biological plausibility of DiffInfinite data is evaluated in a survey by ten experienced pathologists as well as a downstream classification and segmentation task. Samples from the model score strongly on anti-copying metrics which is relevant for the protection of patient data.