Author

Basile Jay

Centre National de la Recherche ScientifiqueORCID 0000-0001-8573-8722Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Microbiology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:transcription & RNA processing· 1

Frequent Co-Authors

Christine NeuveutiD· 2 shared Joao Diogo DiasiD· 2 shared Nazim SaricaiD· 2 shared Oceane LopeziD· 2 shared David DuranteliD· 1 shared Gabrielle Pozo· 1 shared Gaël Petitjean· 1 shared Irene Kasindi MekiiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersMicrobiology

Christine NeuveutORCID

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2 papers

Recent·Most cited

MicrobiologyPLoS PathogensPeer-reviewedJul 30, 2026

ddOTs: a multiplexed quantitative ddPCR approach for resolving overlapping hepatitis B virus transcripts to decipher cccDNA-driven transcription

Nazim Sarica, Oceane Lopez, Joao Diogo Dias…·Christine Neuveut

The paper introduces ddOTs, a ddPCR method to quantify overlapping HBV transcripts, enabling precise analysis of cccDNA-driven transcription and RNA stability.

1 citation

humanbulk RNA-seq

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MicrobiologybioRxivPreprintNov 10, 2025

The histone variant H2A.Z and its chaperone SRCAP are required for RNA polymerase II to access HBV chromatin

Basile Jay, Océane Lopez, Laetitia Gérossier…·Joao Diogo Dias

This study identifies H2A.Z and SRCAP as essential for HBV cccDNA transcription by promoting chromatin accessibility and RNA polymerase II recruitment.

DOI 10.1101/2025.11.10.687638

humanChIP-seq

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