Author

Delphine Bacq-Daian

Commissariat à l'Énergie Atomique et aux Énergies Alternatives

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 3 Approach:benchmark study· 1 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Jean‐François DeleuzeiD· 3 shared Robert OlasoiD· 3 shared Vincent MeyeriD· 3 shared Florian SandroniD· 2 shared AIMS-2-Trials A-Reps group· 1 shared Alexandre MathieuiD· 1 shared Aline LefebvreiD· 1 shared Aline VitraciD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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3 shared papersGenomics

Jean‐François DeleuzeORCID

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Author profile →

3 papers

Recent·Most cited

Unraveling the potential of short and long read sequencing for human genome profiling

Aurélie Leduc, Asmae Bachr, Florian Sandron, Marc Délepine, Damien Delafoy, Cédric Fund, Christian Daviaud, Stéphane Meslage, Violette Turon, Delphine Bacq-Daian, Francis Rousseau, Robert Olaso, Jean‐François Deleuze, Zuzana Gerber, Vincent Meyer

This study compares short and long read sequencing technologies for human genome profiling, finding they are equivalent for SNVs but long reads excel in structural variants and haplotype phasing.

bioRxiv · Apr 22, 2026 · PreprintGenomics

LEAP-InovAND a multiscale resource to explore genetics, brain imaging and clinical data in autism

Mathis Fleury, Zakaria Mougin, Claire S. Leblond, Freddy Cliquet, Alexandre Mathieu, Bethany F. M. Oakley, Anna Maruani, Jean‐Madeleine de Sainte Agathe, Selin Korkmaz, Rosemary Holt, Aline Vitrac, Frédérique Amsellem, Aria Batut, Gaelle Botton-Amiot, Thomas Rolland, , Thomas Bourgeron

The paper introduces a multiscale resource integrating genetics, brain imaging, and clinical data from autistic individuals and their relatives to explore genetic and neurobiological patterns in autism.

medRxiv · Nov 24, 2025 · PreprintGenetic & Genomic Medicine

Genetic population structure across Brittany and the downstream Loire basin provides new insights on the demographic history of Western Europe

Isabel Alves, Joanna Giemza, Michaël G. B. Blum, Carolina Bernhardsson, Stéphanie Chatel, Matilde Karakachoff, Aude Saint Pierre, Anthony F. Herzig, Robert Olaso, Martial Monteil, Véronique Gallien, Élodie Cabot, Emma Svensson, Delphine Bacq-Daian, Estelle Baron, , Christian Dina C

The paper analyzes genetic structure in Brittany and the Loire basin to understand Western Europe's demographic history, finding increased population differentiation linked to steppe and Neolithic ancestry.

bioRxiv · Feb 3, 2022 · PreprintGenetics