Author

Rocío Chamorro González

Max Delbrück CenterORCID 0000-0002-5653-7259Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:variant calling· 2 Approach:deep learning· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:long-read sequencing· 1

Frequent Co-Authors

Anton George HensseniD· 2 shared Angelika EggertiD· 1 shared Anna M. Schroeer· 1 shared Annabell SzymanskyiD· 1 shared Annika WinkleriD· 1 shared Barbara HeroiD· 1 shared Bastiaan SpanjaardiD· 1 shared Christina Stangl· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersCancer Biology

Anton George HenssenORCID

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2 papers

Recent·Most cited

Quantitative and sensitive neuroblastoma minimal residual disease detection using extrachromosomal DNA (ecDNA) breakpoints

Annabell Szymansky, Falk Hertwig, Annika Winkler, Rocío Chamorro González, Konstantin Helmsauer, Anna M. Schroeer, MJ Witthauer, Eliz Karaman, Marco Lodrini, Jasmin Wünschel, Nadine Wittstruck, Steffen Fuchs, Jessica Theißen, Barbara Hero, Richard P. Koche, , Johannes Hubertus Schulte

This study develops a method to detect minimal residual disease in neuroblastoma using ecDNA breakpoints, achieving high sensitivity and specificity in bone marrow samples.

bioRxiv · Sep 12, 2026 · PreprintCancer Biology

Partner-independent fusion gene detection by multiplexed CRISPR/Cas9 enrichment and long-read Nanopore sequencing

Christina Stangl, Sam de Blank, Ivo Renkens, Liset Westera, Tamara C. A. I. Verbeek, Jose Espejo Valle-Inclán, Rocío Chamorro González, Anton George Henssen, Markus J. van Roosmalen, Ronald W. Stam, Emile E. Voest, Wigard P. Kloosterman, Gijs W van Haaften, Glen R. Monroe

This paper introduces FUDGE, a method for detecting fusion genes using CRISPR/Cas9 enrichment and long-read sequencing, achieving high sensitivity and specificity across various cancer types.

Nature Communications · Jun 5, 2020Peer-reviewedGenomics