Author

Duncan Berger

The Francis Crick InstitutePrimary ORCID profile (0000-0002-2017-6623 · 8 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Duncan BergeriD8 papers · Wellcome Sanger Institute

Biology Disciplines

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Molecular Biology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

Aleksandra MichrowskaiD· 1 shared Enkai JiniD· 1 shared Fairouz IbrahimiD· 1 shared Folkert Jacobus van WerveniD· 1 shared Hector Cross· 1 shared James R. BootiD· 1 shared Kamil R. KranciD· 1 shared Laura MasinoiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperMolecular Biology

Aleksandra MichrowskaORCID

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1 paper

Recent·Most cited

Cellular context restricts a promiscuous m6A reader IDR to a single functional effector interface for mRNA decay

Wei Yee Chan, Enkai Jin, Hector Cross, Laura Masino, Fairouz Ibrahim, Waleed S. Albihlal, Duncan Berger, James R. Boot, Aleksandra Michrowska, Stéphane Mouilleron, Mark J. Skehel, Kamil R. Kranc, Folkert Jacobus van Werven

Yeast m6A reader Pho92 uses one helical hydrophobic interface in its disordered region to engage Caf40; a single L35A substitution halts m6A-transcript decay in meiosis.

bioRxiv · Aug 5, 2026 · PreprintMolecular Biology✦ In-depth digest