Arrate Muñoz-Barrutia

Wanlu Lei, Caterina Fuster-Barceló, Gabriel Reder et al.

We present the BioImage$.$IO Chatbot, an AI assistant powered by Large Language Models and supported by a community-driven knowledge base and toolset. This chatbot is designed to cater to a wide range of user needs through a flexible extension mechanism that spans from information retrieval to AI-enhanced analysis and microscopy control. Embracing open-source principles, the chatbot is designed to evolve through community contributions. By simplifying navigation through the intricate bioimaging landscape, the BioImage$.$IO Chatbot empowers life sciences to progress by leveraging the collective expertise and innovation of its users.

Pedro M. Gordaliza, Juan José Vaquero, Arrate Muñoz-Barrutia

The development of new treatments often requires clinical trials with translational animal models using (pre)-clinical imaging to characterize inter-species pathological processes. Deep Learning (DL) models are commonly used to automate retrieving relevant information from the images. Nevertheless, they typically suffer from low generability and explainability as a product of their entangled design, resulting in a specific DL model per animal model. Consequently, it is not possible to take advantage of the high capacity of DL to discover statistical relationships from inter-species images. To alleviate this problem, in this work, we present a model capable of extracting disentangled information from images of different animal models and the mechanisms that generate the images. Our method is located at the intersection between deep generative models, disentanglement and causal representation learning. It is optimized from images of pathological lung infected by Tuberculosis and is able: a) from an input slice, infer its position in a volume, the animal model to which it belongs, the damage present and even more, generate a mask covering the whole lung (similar overlap measures to the nnU-Net), b) generate realistic lung images by setting the above variables and c) generate counterfactual images, namely, healthy versions of a damaged input slice.

Caterina Fuster-Barceló, Claudia Castrillón, Laura Rodrigo-Muñoz et al.

We present OREHAS (Optimized Recognition & Evaluation of volumetric Hydrops in the Auditory System), the first fully automatic pipeline for volumetric quantification of endolymphatic hydrops (EH) from routine 3D-SPACE-MRC and 3D-REAL-IR MRI. The system integrates three components -- slice classification, inner ear localization, and sequence-specific segmentation -- into a single workflow that computes per-ear endolymphatic-to-vestibular volume ratios (ELR) directly from whole MRI volumes, eliminating the need for manual intervention. Trained with only 3 to 6 annotated slices per patient, OREHAS generalized effectively to full 3D volumes, achieving Dice scores of 0.90 for SPACE-MRC and 0.75 for REAL-IR. In an external validation cohort with complete manual annotations, OREHAS closely matched expert ground truth (VSI = 74.3%) and substantially outperformed the clinical syngo.via software (VSI = 42.5%), which tended to overestimate endolymphatic volumes. Across 19 test patients, vestibular measurements from OREHAS were consistent with syngo.via, while endolymphatic volumes were systematically smaller and more physiologically realistic. These results show that reliable and reproducible EH quantification can be achieved from standard MRI using limited supervision. By combining efficient deep-learning-based segmentation with a clinically aligned volumetric workflow, OREHAS reduces operator dependence, ensures methodological consistency. Besides, the results are compatible with established imaging protocols. The approach provides a robust foundation for large-scale studies and for recalibrating clinical diagnostic thresholds based on accurate volumetric measurements of the inner ear.

Roman Kinakh, Gonzalo R. Ríos-Muñoz, Arrate Muñoz-Barrutia

Accurate assessment of PD-L1 expression is critical for guiding immunotherapy, yet current immunohistochemistry (IHC) based methods are resource-intensive. We present nnUNet-B: a Bayesian segmentation framework that infers PD-L1 expression directly from H&E-stained histology images using Multimodal Posterior Sampling (MPS). Built upon nnUNet-v2, our method samples diverse model checkpoints during cyclic training to approximate the posterior, enabling both accurate segmentation and epistemic uncertainty estimation via entropy and standard deviation. Evaluated on a dataset of lung squamous cell carcinoma, our approach achieves competitive performance against established baselines with mean Dice Score and mean IoU of 0.805 and 0.709, respectively, while providing pixel-wise uncertainty maps. Uncertainty estimates show strong correlation with segmentation error, though calibration remains imperfect. These results suggest that uncertainty-aware H&E-based PD-L1 prediction is a promising step toward scalable, interpretable biomarker assessment in clinical workflows.

Laura Nicolás-Sáenz, Agapito Ledezma, Javier Pascau et al.

In any computer vision task involving color images, a necessary step is classifying pixels according to color and segmenting the respective areas. However, the development of methods able to successfully complete this task has proven challenging, mainly due to the gap between human color perception, linguistic color terms, and digital representation. In this paper, we propose a novel method combining geometric analysis of color theory, fuzzy color spaces, and multi-label systems for the automatic classification of pixels according to 12 standard color categories (Green, Yellow, Light Orange, Deep Orange, Red, Pink, Purple, Ultramarine, Blue, Teal, Brown, and Neutral). Moreover, we present a robust, unsupervised, unbiased strategy for color naming based on statistics and color theory. ABANICCO was tested against the state of the art in color classification and with the standarized ISCC-NBS color system, providing accurate classification and a standard, easily understandable alternative for hue naming recognizable by humans and machines. We expect this solution to become the base to successfully tackle a myriad of problems in all fields of computer vision, such as region characterization, histopathology analysis, fire detection, product quality prediction, object description, and hyperspectral imaging.

Estibaliz Gómez-de-Mariscal, Hasini Jayatilaka, Özgün Çiçek et al.

Studying cell morphology changes in time is critical to understanding cell migration mechanisms. In this work, we present a deep learning-based workflow to segment cancer cells embedded in 3D collagen matrices and imaged with phase-contrast microscopy. Our approach uses transfer learning and recurrent convolutional long-short term memory units to exploit the temporal information from the past and provide a consistent segmentation result. Lastly, we propose a geometrical-characterization approach to studying cancer cell morphology. Our approach provides stable results in time, and it is robust to the different weight initialization or training data sampling. We introduce a new annotated dataset for 2D cell segmentation and tracking, and an open-source implementation to replicate the experiments or adapt them to new image processing problems.

Lorena Gallego-Viñarás, Juan Miguel Mira-Tomás, Anna Michela-Gaeta et al.

Alzheimer's disease (AD) and sleep disorders exhibit a close association, where disruptions in sleep patterns often precede the onset of Mild Cognitive Impairment (MCI) and early-stage AD. This study delves into the potential of utilizing sleep-related electroencephalography (EEG) signals acquired through polysomnography (PSG) for the early detection of AD. Our primary focus is on exploring semi-supervised Deep Learning techniques for the classification of EEG signals due to the clinical scenario characterized by the limited data availability. The methodology entails testing and comparing the performance of semi-supervised SMATE and TapNet models, benchmarked against the supervised XCM model, and unsupervised Hidden Markov Models (HMMs). The study highlights the significance of spatial and temporal analysis capabilities, conducting independent analyses of each sleep stage. Results demonstrate the effectiveness of SMATE in leveraging limited labeled data, achieving stable metrics across all sleep stages, and reaching 90% accuracy in its supervised form. Comparative analyses reveal SMATE's superior performance over TapNet and HMM, while XCM excels in supervised scenarios with an accuracy range of 92 - 94%. These findings underscore the potential of semi-supervised models in early AD detection, particularly in overcoming the challenges associated with the scarcity of labeled data. Ablation tests affirm the critical role of spatio-temporal feature extraction in semi-supervised predictive performance, and t-SNE visualizations validate the model's proficiency in distinguishing AD patterns. Overall, this research contributes to the advancement of AD detection through innovative Deep Learning approaches, highlighting the crucial role of semi-supervised learning in addressing data limitations.

Daniel Franco-Barranco, Julio Pastor-Tronch, Aitor Gonzalez-Marfil et al.

Accurate segmentation of electron microscopy (EM) volumes of the brain is essential to characterize neuronal structures at a cell or organelle level. While supervised deep learning methods have led to major breakthroughs in that direction during the past years, they usually require large amounts of annotated data to be trained, and perform poorly on other data acquired under similar experimental and imaging conditions. This is a problem known as domain adaptation, since models that learned from a sample distribution (or source domain) struggle to maintain their performance on samples extracted from a different distribution or target domain. In this work, we address the complex case of deep learning based domain adaptation for mitochondria segmentation across EM datasets from different tissues and species. We present three unsupervised domain adaptation strategies to improve mitochondria segmentation in the target domain based on (1) state-of-the-art style transfer between images of both domains; (2) self-supervised learning to pre-train a model using unlabeled source and target images, and then fine-tune it only with the source labels; and (3) multi-task neural network architectures trained end-to-end with both labeled and unlabeled images. Additionally, we propose a new training stopping criterion based on morphological priors obtained exclusively in the source domain. We carried out all possible cross-dataset experiments using three publicly available EM datasets. We evaluated our proposed strategies on the mitochondria semantic labels predicted on the target datasets. The methods introduced here outperform the baseline methods and compare favorably to the state of the art. In the absence of validation labels, monitoring our proposed morphology-based metric is an intuitive and effective way to stop the training process and select in average optimal models.

Daniel Franco-Barranco, Arrate Muñoz-Barrutia, Ignacio Arganda-Carreras

Electron microscopy (EM) allows the identification of intracellular organelles such as mitochondria, providing insights for clinical and scientific studies. In recent years, a number of novel deep learning architectures have been published reporting superior performance, or even human-level accuracy, compared to previous approaches on public mitochondria segmentation datasets. Unfortunately, many of these publications do not make neither the code nor the full training details public to support the results obtained, leading to reproducibility issues and dubious model comparisons. For that reason, and following a recent code of best practices for reporting experimental results, we present an extensive study of the state-of-the-art deep learning architectures for the segmentation of mitochondria on EM volumes, and evaluate the impact in performance of different variations of 2D and 3D U-Net-like models for this task. To better understand the contribution of each component, a common set of pre- and post-processing operations has been implemented and tested with each approach. Moreover, an exhaustive sweep of hyperparameters values for all architectures have been performed and each configuration has been run multiple times to report the mean and standard deviation values of the evaluation metrics. Using this methodology, we found very stable architectures and hyperparameter configurations that consistently obtain state-of-the-art results in the well-known EPFL Hippocampus mitochondria segmentation dataset. Furthermore, we have benchmarked our proposed models on two other available datasets, Lucchi++ and Kasthuri++, where they outperform all previous works. The code derived from this research and its documentation are publicly available.