Recent research · 2026
A better control for ATAC-seq
We showed that using whole-genome sequencing as a control improves ATAC-seq peak calling.
NAR Genomics and Bioinformatics
Explore the publicationsBioinformatics · Montpellier, France
I analyse sequencing data to understand blood disorders and gene regulation. I also build tools that make genomic analysis easier to use.
Recent research · 2026
We showed that using whole-genome sequencing as a control improves ATAC-seq peak calling.
NAR Genomics and Bioinformatics
Explore the publicationsVariant analysis
Explore and prioritise variants in whole-exome sequencing data.
Nanopore sequencing
An amplicon-based sequencing pipeline for tracking pathogen variants.
Bioinformatician and data scientist working on sequencing data since 2018, at IGMM, Institut Imagine and IRCM.
Much of my work concerns how red blood cells are made and what goes wrong in inherited blood disorders: single-cell analysis of CD34+ cells in sickle cell anaemia, a Myb enhancer deletion in β-thalassaemia, and the ZEB1–GATA2–KLF1 switch published in Nucleic Acids Research in 2026. At IRCM, I also worked on cancer genomics.
I also develop machine-learning methods for gene regulation. RegFiT (manuscript in preparation) reconstructs enhancer-based gene regulatory networks from paired ATAC-seq and RNA-seq data, from as few as two experimental conditions. Applied to eight stages of erythroid differentiation, it identified a functional interaction between the erythroid transcription factor KLF1 and ZEB1, which was then validated experimentally.
I have supervised bioinformatics engineers and doctoral students, and managed bioinformatics and data science projects at Institut Imagine from 2025 to 2026. Since October 2026 I am back at IGMM, and I continue to collaborate with members of the GR-Ex Laboratory of Excellence (InIdex GR-Ex).
University of Montpellier
Bioinformatics & Data Science
267 Citations, h-index: 8
Montpellier, France
Montpellier, France
Montpellier, France
Paris, France
Montpellier, France
NAR Genomics and Bioinformatics (2026)
View PublicationNucleic Acids Research (2026)
Selected as an NAR Breakthrough Article — the journal's highest distinction, reserved for the top 1–2% of papers. Alexia Kinoo, Virginie Deleuze and Mohammad Salma contributed equally as co-first authors.
View PublicationAmerican Journal of Hematology (2026)
View PublicationNature Communications (2025)
View PublicationHemaSphere (2025)
View PublicationScientific Reports (2025)
View PublicationBlood (2023)
View PublicationIScience (2023)
View PublicationEpigenetics & Chromatin (2023)
Developed a web-based tool that significantly streamlines WES data analysis, offering extensive gene and variant filtering, clustering, and enrichment tools without requiring complex bioinformatics skills.
View PublicationBlood Cells, Molecules, and Diseases (2023)
View PublicationBioinformatics (2022)
View PublicationJournal of Clinical Investigation (2021)
View PublicationBlood (2021)
Demonstrates how p53 activation during ribosome biogenesis plays a crucial role in regulating normal erythroid differentiation processes.
View PublicationMethods in Molecular Biology (2017)
View PublicationScientia Horticulturae (2014) - 41 Citations
View PublicationProtoplasma (2014) - 23 Citations
View Publication원예과학기술지 (2012)
View PublicationGoogle Scholar metrics as of .
Publications
Citations
h-index
i10-index
A web-based tool for exploring and prioritizing variants in whole-exome sequencing data. Features extensive filtering, clustering, and enrichment capabilities without requiring complex bioinformatics skills.
Nanopore-based pipeline for tracking pathogenic variants. Developed for real-time monitoring of SARS-CoV-2 and other pathogen variants using Oxford Nanopore sequencing.
Comprehensive suite of bioinformatics pipelines for multi-omics analysis including RNA-Seq, ATAC-Seq, ChIP-Seq, and single-cell sequencing with automated QC and reporting.
Machine learning models for biomarker identification and predictive analysis in cancer genomics using TensorFlow and scikit-learn frameworks.
Get in touch about collaborations on sequencing data, chromatin accessibility or gene regulatory networks, questions about Var|Decrypt or ONTdeCIPHER, or job opportunities.
Montpellier, France