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Mollet, B.

Publications and source records attributed to Mollet, B..

2 recordsLinked to original sources

Artificial Metabolic Networks: enabling neural computation with metabolic networks

Constraint-based metabolic models have been used for decades to predict the phenotype of microorganisms in different environments. However, quantitative predictions are limited unless labor-intensive measurements of media uptake fluxes are performed. We show how hybrid neural-mechanistic models can serve as an architecture for machine learning providing a way to improve phenotype predictions. We illustrate our hybrid models with growth rate predictions of Escherichia coli and Pseudomonas putida grown in different media and with phenotype predictions of gene knocked-out Escherichia coli mutants. Our neural-mechanistic models systematically outperform constraint-based models and require training set sizes orders of magnitude smaller than classical machine learning methods. Our hybrid approach opens a doorway to enhancing constraint-based modeling: instead of constraining mechanistic models with additional experimental measurements, our hybrid models grasp the power of machine learning while fulfilling mechanistic constrains, thus saving time and resources in typical systems biology or biological engineering projects.

systems biology↗

Inferring functionally relevant molecular tissue substructures by agglomerative clustering of digitized spatial transcriptomes

Developments on spatial transcriptomics (ST) are providing means to interrogate organ/tissue architecture from the angle of the gene programs defining their molecular complexity. However, computational methods to analyze ST data under-exploits the spatial signature retrieved within the maps. Inspired by contextual pixel classification strategies applied to image analysis, we have developed MULTILAYER, allowing to stratify ST maps into functionally-relevant molecular substructures. For it, MULTILAYER applies agglomerative clustering strategies within contiguous locally-defined transcriptomes (herein defined as gene expression elements or Gexels), combined with community detection methods for graph partitioning. MULTILAYER has been evaluated over multiple public ST data, including developmental tissues but also tumor biopsies. Its performance has been challenged for the processing of high-resolution ST maps and it has been used for an enhanced comparison of multiple public tissue biopsies issued from a cancerous prostate. MULTILAYER provides a digital perspective for the analysis of spatially-resolved transcriptomes and anticipates the application of contextual gexel classification strategies for developing self-supervised molecular diagnostics solutions. Overall, the development of MULTILAYER anticipates the application of contextual gexel classification strategies for developing self-supervised molecular diagnostics solutions.

bioinformatics↗