Author

Büşra Erarslan-Uysal

German Cancer Research CenterORCID 0000-0002-7135-2201Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Organism:human· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:imaging· 1 Approach:machine learning (classical)· 1 Assay:scATAC-seq· 1

Frequent Co-Authors

Andreas E. KulozikiD· 2 shared Jan O. KorbeliD· 2 shared Patrick HasenfeldiD· 2 shared Tobias RauschiD· 2 shared Aliaksandr A. HalavatyiiD· 1 shared Alice GaiattoiD· 1 shared Álvaro AndradesiD· 1 shared Ashley D. SandersiD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenomics

Andreas E. KulozikORCID

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2 papers

Recent·Most cited

Origins of de novo chromosome rearrangements unveiled by coupled imaging and genomics

Marco Raffaele Cosenza, Alice Gaiatto, Büşra Erarslan-Uysal, Álvaro Andrades, Nina Luisa Sautter, Marina Simunovic, Michael Jendrusch, Sonia Zumalave, Tobias Rausch, Aliaksandr A. Halavatyi, Eva‐Maria Geissen, Joshua Eigenmann, Thomas Weber, Patrick Hasenfeld, Eva Benito, , Jan O. Korbel

The paper introduces MAGIC, a platform combining imaging and genomics to study de novo chromosome rearrangements, finding that dicentric chromosomes initiate CA events and TP53 deficiency increases CA rates.

Nature · Oct 29, 2025Peer-reviewedGenomics

Haplotype-aware single-cell multiomics uncovers functional effects of somatic structural variation

Hyobin Jeong, Karen Grimes, Peter‐Martin Bruch, Tobias Rausch, Patrick Hasenfeld, Radhakrishnan Sabarinathan, David Porubskỳ, Sophie A. Herbst, Büşra Erarslan-Uysal, Johann-Christoph Jann, Tobias Marschall, Daniel Nowak, Jean‐Pierre Bourquin, Andreas E. Kulozik, Sascha Dietrich, , Jan O. Korbel

This paper introduces scNOVA, a method to analyze somatic structural variants in single-cell multiomics data, revealing their functional impacts on gene regulation and cancer pathways.

bioRxiv · Nov 11, 2021 · PreprintGenomics