arXiv subjects

Anaïs Baudot

Publications and source records attributed to Anaïs Baudot.

7 recordsLinked to original sources

arXiv2026

MODIS: Multi-Omics Data Integration for Small and unpaired datasets

An important objective in computational biology is the efficient integration of multi-omics data. The task of integration comes with challenges: multi-omics data are most often unpaired (requiring diagonal integration), partially labeled with information about biological conditions, and in some situations such as rare diseases, only very small datasets are available. We present MODIS, a semi supervised framework designed to account for these particular challenges. To address the challenge of very small datasets, we propose to exploit the information contained in larger multi-omics databases by training our model on a large reference database and a small target dataset simultaneously, effectively turning the challenge into a problem of learning with class imbalance. MODIS performs diagonal integration on unpaired samples, leveraging class-labels to align modalities despite class imbalance and data scarcity. The architecture combines multiple variational auto-encoders, a class classifier and an adversarially trained modality classifier. To ensure training stability, we adapted a regularized relativistic GAN loss to this setting. We first validate MODIS on a synthetic dataset to assess the level of supervision needed for accurate alignment and to quantify the impact of class imbalance on predictive performance. We then apply our approach to the large public TCGA database, considering between 10 and 34 classes (cancer types and normal tissue). MODIS demonstrates high prediction accuracy, robust performance with limited supervision, and stability to class imbalance. These results position MODIS as a promising solution for challenging integration scenarios, particularly diagonal integration with a small number of samples, typical of rare diseases studies. The code is available at https://github.com/VILLOUTREIXLab/MODIS.

cs.LG↗

arXiv2026

On the Promises and Limits of Multi-omics Integration for Deconvolution: The HADACA3 Benchmark

Understanding the cellular composition of complex tissues, such as tumors, is a key challenge in biology and medicine. A common approach, known as deconvolution, aims to estimate the cellular composition from bulk molecular measurements. With the growing availability of multiple types of molecular data, it is often assumed that combining data sources should improve deconvolution performance. Here, we present HADACA3, a community-driven benchmark designed to evaluate this assumption. We conducted a four-day collaborative competition followed by a large-scale computational benchmark, testing more than 250,000 analysis pipelines across nine datasets with matched DNA methylation (DNAm) and RNA profiles, representing a wide range of biological and experimental conditions. Our framework jointly evaluates the impact of preprocessing, feature selection, modeling, and integration strategies. We find that DNAm alone achieves the highest median performance across datasets, making it the most stable and reliable single-modality approach. However, multi-omics integration strategies can regularly achieve higher top performance in specific datasets and pipeline configurations. Among the tested strategies, late integration based on error-weighted averaging provides a strong and reliable baseline, while non-linear early integration methods, such as optimal transport, show promising results on real biological datasets. Overall, our results show that multi-omics integration does not systematically improve average performance over DNAm alone, but can improve best-case performance in specific settings. This highlights a trade-off between robustness and peak performance, and emphasizes the importance of aligning integration strategies with the statistical properties of the data. All data, code, and evaluation tools are publicly available to support reproducible research and future method development.

q-bio.QM↗

arXiv2024

Refining Boolean models with the partial most permissive scheme

Motivation: In systems biology, modelling strategies aim to decode how molecular components interact to generate dynamical behaviour. Boolean modelling is more and more used, but the description of the dynamics from two-levels components may be too limited to capture certain dynamical properties. %However, in Boolean models, the description of the dynamics may be too limited to capture certain dynamical properties. Multivalued logical models can overcome this limitation by allowing more than two levels for each component. However, multivaluing a Boolean model is challenging. Results: We present MRBM, a method for efficiently identifying the components of a Boolean model to be multivalued in order to capture specific fixed-point reachabilities in the asynchronous dynamics. To this goal, we defined a new updating scheme locating reachability properties in the most permissive dynamics. MRBM is supported by mathematical demonstrations and illustrated on a toy model and on two models of stem cell differentiation.

q-bio.MN↗

arXiv2024

Current and future directions in network biology

Network biology is an interdisciplinary field bridging computational and biological sciences that has proved pivotal in advancing the understanding of cellular functions and diseases across biological systems and scales. Although the field has been around for two decades, it remains nascent. It has witnessed rapid evolution, accompanied by emerging challenges. These challenges stem from various factors, notably the growing complexity and volume of data together with the increased diversity of data types describing different tiers of biological organization. We discuss prevailing research directions in network biology and highlight areas of inference and comparison of biological networks, multimodal data integration and heterogeneous networks, higher-order network analysis, machine learning on networks, and network-based personalized medicine. Following the overview of recent breakthroughs across these five areas, we offer a perspective on the future directions of network biology. Additionally, we offer insights into scientific communities, educational initiatives, and the importance of fostering diversity within the field. This paper establishes a roadmap for an immediate and long-term vision for network biology.

q-bio.MN↗

arXiv2023

Zoo Guide to Network Embedding

Networks have provided extremely successful models of data and complex systems. Yet, as combinatorial objects, networks do not have in general intrinsic coordinates and do not typically lie in an ambient space. The process of assigning an embedding space to a network has attracted lots of interest in the past few decades, and has been efficiently applied to fundamental problems in network inference, such as link prediction, node classification, and community detection. In this review, we provide a user-friendly guide to the network embedding literature and current trends in this field which will allow the reader to navigate through the complex landscape of methods and approaches emerging from the vibrant research activity on these subjects.

cs.SI↗

arXiv2022

Universal Multilayer Network Exploration by Random Walk with Restart

The amount and variety of data is increasing drastically for several years. These data are often represented as networks, which are then explored with approaches arising from network theory. Recent years have witnessed the extension of network exploration methods to leverage more complex and richer network frameworks. Random walks, for instance, have been extended to explore multilayer networks. However, current random walk approaches are limited in the combination and heterogeneity of network layers they can handle. New analytical and numerical random walk methods are needed to cope with the increasing diversity and complexity of multilayer networks. We propose here MultiXrank, a Python package that enables Random Walk with Restart (RWR) on any kind of multilayer network with an optimized implementation. This package is supported by a universal mathematical formulation of the RWR. We evaluated MultiXrank with leave-one-out cross-validation and link prediction, and introduced protocols to measure the impact of the addition or removal of multilayer network data on prediction performances. We further measured the sensitivity of MultiXrank to input parameters by in-depth exploration of the parameter space. Finally, we illustrate the versatility of MultiXrank with different use-cases of unsupervised node prioritization and supervised classification in the context of human genetic diseases.

cs.LG↗

arXiv2021

MultiVERSE: a multiplex and multiplex-heterogeneous network embedding approach

Network embedding approaches are gaining momentum to analyse a large variety of networks. Indeed, these approaches have demonstrated their efficiency for tasks such as community detection, node classification, and link prediction. However, very few network embedding methods have been specifically designed to handle multiplex networks, i.e. networks composed of different layers sharing the same set of nodes but having different types of edges. Moreover, to our knowledge, existing approaches cannot embed multiple nodes from multiplex-heterogeneous networks, i.e. networks composed of several layers containing both different types of nodes and edges. In this study, we propose MultiVERSE, an extension of the VERSE method with Random Walks with Restart on Multiplex (RWR-M) and Multiplex-Heterogeneous (RWR-MH) networks. MultiVERSE is a fast and scalable method to learn node embeddings from multiplex and multiplex-heterogeneous networks. We evaluate MultiVERSE on several biological and social networks and demonstrate its efficiency. MultiVERSE indeed outperforms most of the other methods in the tasks of link prediction and network reconstruction for multiplex network embedding, and is also efficient in the task of link prediction for multiplex-heterogeneous network embedding. Finally, we apply MultiVERSE to study rare disease-gene associations using link prediction and clustering. MultiVERSE is freely available on github at https://github.com/Lpiol/MultiVERSE.

cs.LG↗