Richard D. Paul

CV
h-index34
5papers
10citations
Novelty39%
AI Score37

5 Papers

CVSep 25, 2024
Parameter-efficient Bayesian Neural Networks for Uncertainty-aware Depth Estimation

Richard D. Paul, Alessio Quercia, Vincent Fortuin et al.

State-of-the-art computer vision tasks, like monocular depth estimation (MDE), rely heavily on large, modern Transformer-based architectures. However, their application in safety-critical domains demands reliable predictive performance and uncertainty quantification. While Bayesian neural networks provide a conceptually simple approach to serve those requirements, they suffer from the high dimensionality of the parameter space. Parameter-efficient fine-tuning (PEFT) methods, in particular low-rank adaptations (LoRA), have emerged as a popular strategy for adapting large-scale models to down-stream tasks by performing parameter inference on lower-dimensional subspaces. In this work, we investigate the suitability of PEFT methods for subspace Bayesian inference in large-scale Transformer-based vision models. We show that, indeed, combining BitFit, DiffFit, LoRA, and CoLoRA, a novel LoRA-inspired PEFT method, with Bayesian inference enables more robust and reliable predictive performance in MDE.

IVDec 7, 2025
Physics-Guided Diffusion Priors for Multi-Slice Reconstruction in Scientific Imaging

Laurentius Valdy, Richard D. Paul, Alessio Quercia et al.

Accurate multi-slice reconstruction from limited measurement data is crucial to speed up the acquisition process in medical and scientific imaging. However, it remains challenging due to the ill-posed nature of the problem and the high computational and memory demands. We propose a framework that addresses these challenges by integrating partitioned diffusion priors with physics-based constraints. By doing so, we substantially reduce memory usage per GPU while preserving high reconstruction quality, outperforming both physics-only and full multi-slice reconstruction baselines for different modalities, namely Magnetic Resonance Imaging (MRI) and four-dimensional Scanning Transmission Electron Microscopy (4D-STEM). Additionally, we show that the proposed method improves in-distribution accuracy as well as strong generalization to out-of-distribution datasets.

CVOct 7, 2025Code
acia-workflows: Automated Single-cell Imaging Analysis for Scalable and Deep Learning-based Live-cell Imaging Analysis Workflows

Johannes Seiffarth, Keitaro Kasahara, Michelle Bund et al.

Live-cell imaging (LCI) technology enables the detailed spatio-temporal characterization of living cells at the single-cell level, which is critical for advancing research in the life sciences, from biomedical applications to bioprocessing. High-throughput setups with tens to hundreds of parallel cell cultivations offer the potential for robust and reproducible insights. However, these insights are obscured by the large amount of LCI data recorded per experiment. Recent advances in state-of-the-art deep learning methods for cell segmentation and tracking now enable the automated analysis of such large data volumes, offering unprecedented opportunities to systematically study single-cell dynamics. The next key challenge lies in integrating these powerful tools into accessible, flexible, and user-friendly workflows that support routine application in biological research. In this work, we present acia-workflows, a platform that combines three key components: (1) the Automated live-Cell Imaging Analysis (acia) Python library, which supports the modular design of image analysis pipelines offering eight deep learning segmentation and tracking approaches; (2) workflows that assemble the image analysis pipeline, its software dependencies, documentation, and visualizations into a single Jupyter Notebook, leading to accessible, reproducible and scalable analysis workflows; and (3) a collection of application workflows showcasing the analysis and customization capabilities in real-world applications. Specifically, we present three workflows to investigate various types of microfluidic LCI experiments ranging from growth rate comparisons to precise, minute-resolution quantitative analyses of individual dynamic cells responses to changing oxygen conditions. Our collection of more than ten application workflows is open source and publicly available at https://github.com/JuBiotech/acia-workflows.

CVMar 12, 2025
How To Make Your Cell Tracker Say "I dunno!"

Richard D. Paul, Johannes Seiffarth, David Rügamer et al.

Cell tracking is a key computational task in live-cell microscopy, but fully automated analysis of high-throughput imaging requires reliable and, thus, uncertainty-aware data analysis tools, as the amount of data recorded within a single experiment exceeds what humans are able to overlook. We here propose and benchmark various methods to reason about and quantify uncertainty in linear assignment-based cell tracking algorithms. Our methods take inspiration from statistics and machine learning, leveraging two perspectives on the cell tracking problem explored throughout this work: Considering it as a Bayesian inference problem and as a classification problem. Our methods admit a framework-like character in that they equip any frame-to-frame tracking method with uncertainty quantification. We demonstrate this by applying it to various existing tracking algorithms including the recently presented Transformer-based trackers. We demonstrate empirically that our methods yield useful and well-calibrated tracking uncertainties.

CVMar 11, 2025
1LoRA: Summation Compression for Very Low-Rank Adaptation

Alessio Quercia, Zhuo Cao, Arya Bangun et al.

Parameter-Efficient Fine-Tuning (PEFT) methods have transformed the approach to fine-tuning large models for downstream tasks by enabling the adjustment of significantly fewer parameters than those in the original model matrices. In this work, we study the "very low rank regime", where we fine-tune the lowest amount of parameters per linear layer for each considered PEFT method. We propose 1LoRA (Summation Low-Rank Adaptation), a compute, parameter and memory efficient fine-tuning method which uses the feature sum as fixed compression and a single trainable vector as decompression. Differently from state-of-the-art PEFT methods like LoRA, VeRA, and the recent MoRA, 1LoRA uses fewer parameters per layer, reducing the memory footprint and the computational cost. We extensively evaluate our method against state-of-the-art PEFT methods on multiple fine-tuning tasks, and show that our method not only outperforms them, but is also more parameter, memory and computationally efficient. Moreover, thanks to its memory efficiency, 1LoRA allows to fine-tune more evenly across layers, instead of focusing on specific ones (e.g. attention layers), improving performance further.