A practical way to prioritize transcription factors by combining motif enrichment, expression, chromatin accessibility, timing and network position.
Metabolism is not merely a source of energy: it continuously instructs gene regulation by shaping chromatin marks and transcriptional programs. Over the years, I have progressively investigated this metabolism-gene regulation axis across complementary biological scales and questions - from skin physiology and microbiome-host interactions to the regulation of cellular senescence and its pathophysiological consequences in aging and cancer. Along this path, I have pursued integrative studies bridging genetics, functional genomics, and systems modeling to understand how metabolic rewiring reshapes regulatory networks in diverse physiological and pathophysiological settings. These projects have provided me with strong expertise in molecular and cellular biology as well as computational biology, including bioinformatics, data integration, and network inference. At the interface of experimental biology and computation, I have developed an integrated view of how metabolic states translate into epigenetic and transcriptional programs that govern cell fate decisions, including senescence. Moving forward, I will build on this framework to address pathophysiological questions at the intersection of metabolism, epigenetics, and aging.
I am currently working at the Montpellier Cancer Research Institute as a postdoctoral fellow, in the unit Molecular Oncogenesis headed by Laurent Le Cam.
PhD in Genetics and Genomics, 2014
Agrocampus Ouest, Rennes, France
MEng in Agronomical Science, 2011
Agrocampus Ouest, Rennes, France
MSc in Cell and Molecular Biology, 2011
Université Rennes 1, Rennes, France
MSc in Environment and Oceanology, 2009
Université des Sciences et Technologies, Lille, France
Metabolism, genome regulation and integrative omics across aging, cancer and skin biology.
My research connects experimental biology, functional genomics and computational modelling to understand how metabolic states reshape regulatory networks. Across projects, I combine molecular and cellular biology with RNA-seq, ATAC-seq, CUT&RUN, ChIP-seq, metabolomics, quantitative genetics and machine-learning strategies to move from omic profiles to mechanistic hypotheses.
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Developing ATAC-seq beyond chromatin accessibility into an all-in-one assay for genetic, epigenetic and aging-related signatures.
Time-resolved multi-omic analyses of senescence to identify regulatory hierarchies, chromatin transitions and vulnerabilities in aging and cancer.
A stringent DNA/RNA-seq framework to distinguish genuine RNA editing events from sequencing, mapping and biological noise.
Combining linkage mapping, whole-genome sequencing, selection signatures and expression QTLs to prioritize causal genes for complex traits.
Representative papers across senescence, metabolism, epigenomics and integrative genomics.
Selected papers highlighting the main biological questions and methodological approaches developed across my research trajectory.
For the complete publication record, open the Publications page from the navigation menu.
Practical notes on genomics, epigenomics and data analysis.
A practical way to prioritize transcription factors by combining motif enrichment, expression, chromatin accessibility, timing and network position.
A practical framework for integrating enhancer states, chromatin signal and gene expression without pretending that nearest gene assignment solves everything.
How to get more biological information from ATAC-seq by looking at fragments, nucleosomes, TSS profiles, footprints and genomic signal.
A generic strategy for using pseudoreplicates and IDR-like thinking to build more robust ChIP-seq and ATAC-seq peak sets.
A compact checklist for deciding whether ChIP-seq or ATAC-seq peak calls are biologically interpretable.
A reusable strategy for extracting dynamic programs from time-course transcriptomic data with splines, clustering and module-level interpretation.
Molecular biology, functional genomics, bioinformatics and omics data analysis.
My teaching connects molecular mechanisms with practical data analysis. I focus on helping biologists move from a biological question to an experimental strategy, a reproducible workflow and a critical interpretation of the results.
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Hands-on training in ChIP-seq, ATAC-seq and MNase-seq analysis, from sequencing quality control to peak calling, normalization and functional interpretation.
Practical training for biologists in RNA-seq data analysis with UNIX, from raw data quality control to alignment, variant calling and transcript model inference.
Training in data visualization with R and ggplot, with emphasis on readable figures, exploratory analysis and reproducible communication of genomic data.
Research mentoring from molecular biology to integrative omics.
I have supervised or co-supervised research trainees at doctoral, Master 2 and Master 1 levels, mainly on projects combining functional genomics, bioinformatics, epigenomics, metabolism and senescence biology.
Mentoring snapshot
Recent projects include ATAC-seq-based detection of cancer mutations and genome instability, p53/E4F1-mediated metabolic and epigenetic reprogramming during senescence, molecular signatures of senescence from multi-omic data, and in vivo metabolic adaptation during aging.