arXiv subjects

Perrine Paul-Gilloteaux

Publications and source records attributed to Perrine Paul-Gilloteaux.

8 recordsLinked to original sources

arXiv2026

From the microscope to High Performance Computing centers, a national effort toward automated data workflows for microscopy facility users in France

Modern biological microscopy routinely generates large and complex image datasets, including multidimensional, multimodal, and time-resolved acquisitions. While imaging technologies have rapidly evolved, data management infrastructures within microscopy facilities often remain fragmented, relying on heterogeneous local solutions that are difficult to maintain, scale, and integrate with High-Performance Computing (HPC) centers and public data repositories. To address these issues, France BioImaging (FBI), the French national infrastructure for biological imaging, has developed FBI.DATA and the associated BioImage Cloud platform. This initiative aims to provide a coordinated national infrastructure connecting microscopy facilities, centralized storage resources, HPC environments, and public bioimaging archives through interoperable and scalable workflows.The proposed architecture combines open-source technologies including OMERO for image management, iRODS for distributed data orchestration, Authentik for federated authentication, and emerging standards such as OME-Zarr and REMBI metadata recommendations. The infrastructure is designed to support the complete imaging data lifecycle, from acquisition and transfer to visualization, analysis, sharing, and long-term archiving. Beyond the technical implementation, this work presents the organizational and governance strategies required to deploy a shared national infrastructure across distributed imaging facilities. We discuss the challenges associated with interoperability, metadata standardization, sustainability, and user adoption, as well as the perspectives opened by tighter integration between imaging data and large-scale computing resources for future AI-driven bioimage analysis workflows.

q-bio.OT↗

arXiv2026

Learn2Reg 2024: New Benchmark Datasets Driving Progress on New Challenges

Medical image registration is critical for clinical applications, and fair benchmarking of different methods is essential for monitoring ongoing progress in the field. To date, the Learn2Reg 2020-2023 challenges have released several complementary datasets and established metrics for evaluations. Building on this foundation, the 2024 edition expands the challenge's scope to cover a wider range of registration scenarios, particularly in terms of modality diversity and task complexity, by introducing three new tasks, including large-scale multi-modal registration and unsupervised inter-subject brain registration, as well as the first microscopy-focused benchmark within Learn2Reg. The new datasets also inspired new method developments, including invertibility constraints, pyramid features, keypoints alignment and instance optimisation. Visit Learn2Reg at https://learn2reg.grand-challenge.org.

eess.IV↗

arXiv2025

F-BIAS: Towards a distributed national core facility for Bioimage Analysis

We discuss in this article the creation and organization of a national core facility for bioimage analysis, based on a distributed team. F-BIAS federates bioimage analysts across France and relies on them to deliver services to the researchers of this territory. The main challenge in implementing this structure is to provide significant scientific value to its members, thereby encouraging their active participation and persuading their respective host teams to support their involvement. F-BIAS accomplished this by creating a professional network that mitigates the negative effects of isolation experienced by its members, who are often the sole bioimage analyst within their local teams, and fosters the development of their technical skills. In a second phase we capitalized on F-BIAS to create a virtual, remotely-operating core facility for bioimage analysis, offering consultations and collaborative project services to the scientific community of France. The services are organized so that they also contribute to the technical proficiency of the analysts. To promote the creation of similar structures, we present and discuss here the organization of this nationally distributed bioimage analysis service core, highlighting successes and challenges.

q-bio.OT↗

arXiv2023

Bio-Image Informatics Index BIII: A unique database of image analysis tools and workflows for and by the bioimaging community

Bio image analysis has recently become one keystone of biological research but biologists tend to get lost in a plethora of available software and the way to adjust available tools to their own image analysis problem. We present BIII, BioImage Informatic Index (www.biii.eu), the result of the first large community effort to bridge the communities of algorithm and software developers, bioimage analysts and biologists, under the form of a web-based knowledge database crowdsourced by these communities. Software tools (> 1300), image databases for benchmarking (>20) and training materials (>70) for bio image analysis are referenced and curated following standards constructed by the community and then reaching a broader audience. Software tools are organized as full protocol of analysis (workflow), specific brick (component) to construct a workflow, or software platform or library (collection). They are described using Edam Bio Imaging, which is iteratively defined using this website. All entries are exposed following FAIR principles and accessible for other usage.

q-bio.QM↗

arXiv2022

Towards deep learning-powered IVF: A large public benchmark for morphokinetic parameter prediction

An important limitation to the development of Artificial Intelligence (AI)-based solutions for In Vitro Fertilization (IVF) is the absence of a public reference benchmark to train and evaluate deep learning (DL) models. In this work, we describe a fully annotated dataset of 704 videos of developing embryos, for a total of 337k images. We applied ResNet, LSTM, and ResNet-3D architectures to our dataset and demonstrate that they overperform algorithmic approaches to automatically annotate stage development phases. Altogether, we propose the first public benchmark that will allow the community to evaluate morphokinetic models. This is the first step towards deep learning-powered IVF. Of note, we propose highly detailed annotations with 16 different development phases, including early cell division phases, but also late cell divisions, phases after morulation, and very early phases, which have never been used before. We postulate that this original approach will help improve the overall performance of deep learning approaches on time-lapse videos of embryo development, ultimately benefiting infertile patients with improved clinical success rates (Code and data are available at https://gitlab.univ-nantes.fr/E144069X/bench_mk_pred.git).

eess.IV↗

arXiv2021

A registration error estimation framework for correlative imaging

Correlative imaging workflows are now widely used in bioimaging and aims to image the same sample using at least two different and complementary imaging modalities. Part of the workflow relies on finding the transformation linking a source image to a target image. We are specifically interested in the estimation of registration error in point-based registration. We propose an application of multivariate linear regression to solve the registration problem allowing us to propose a framework for the estimation of the associated error in the case of rigid and affine transformations and with anisotropic noise. These developments can be used as a decision-support tool for the biologist to analyze multimodal correlative images and are available under Ec-CLEM, an open-source plugin under ICY.

q-bio.QM↗

arXiv2021

QUAREP-LiMi: A community-driven initiative to establish guidelines for quality assessment and reproducibility for instruments and images in light microscopy

In April 2020, the QUality Assessment and REProducibility for Instruments and Images in Light Microscopy (QUAREP-LiMi) initiative was formed. This initiative comprises imaging scientists from academia and industry who share a common interest in achieving a better understanding of the performance and limitations of microscopes and improved quality control (QC) in light microscopy. The ultimate goal of the QUAREP-LiMi initiative is to establish a set of common QC standards, guidelines, metadata models, and tools, including detailed protocols, with the ultimate aim of improving reproducible advances in scientific research. This White Paper 1) summarizes the major obstacles identified in the field that motivated the launch of the QUAREP-LiMi initiative; 2) identifies the urgent need to address these obstacles in a grassroots manner, through a community of stakeholders including, researchers, imaging scientists, bioimage analysts, bioimage informatics developers, corporate partners, funding agencies, standards organizations, scientific publishers, and observers of such; 3) outlines the current actions of the QUAREP-LiMi initiative, and 4) proposes future steps that can be taken to improve the dissemination and acceptance of the proposed guidelines to manage QC. To summarize, the principal goal of the QUAREP-LiMi initiative is to improve the overall quality and reproducibility of light microscope image data by introducing broadly accepted standard practices and accurately captured image data metrics.

q-bio.OT↗

arXiv2020

Cross-modal registration using point clouds and graph-matching in the context of correlative microscopies

Correlative microscopy aims at combining two or more modalities to gain more information than the one provided by one modality on the same biological structure. Registration is needed at different steps of correlative microscopies workflows. Biologists want to select the image content used for registration not to introduce bias in the correlation of unknown structures. Intensity-based methods might not allow this selection and might be too slow when the images are very large. We propose an approach based on point clouds created from selected content by the biologist. These point clouds may be prone to big differences in densities but also missing parts and outliers. In this paper we present a method of registration for point clouds based on graph building and graph matching, and compare the method to iterative closest point based methods.

cs.CV↗