Author

Ruben Cools

KU LeuvenORCID 0009-0004-7484-5564Unclaimed 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 Organism:human· 2 Assay:ATAC-seq· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Assay:long-read sequencing· 1 Assay:scRNA-seq· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Alexandra PančíkováiD· 1 shared Ann SwilleniD· 1 shared Anne S. BassettiD· 1 shared Beverly S. EmanueliD· 1 shared Donna M. McDonald‐McGinniD· 1 shared Erika L. SoucheiD· 1 shared Heidi SegersiD· 1 shared Hilde PeetersiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenomics

Alexandra PančíkováORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintSep 8, 2025

Long-read single-cell genome, transcriptome and open chromatin profiling links genotype to phenotypes.

Alexandra Pančíková, Ruben Cools, Marios Eftychiou…·Jonas Demeulemeester

SPLONGGET enables comprehensive genotype-phenotype analysis by integrating long-read single-cell genome, transcriptome, and open chromatin profiling in thousands of cells.

2 citations

humanscRNA-seq

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GeneticsbioRxivPreprintMar 14, 2024

Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome

Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos…·Joris Robert Vermeesch

The paper investigates the mechanisms behind the high incidence of 22q11.2 deletion syndrome by analyzing recombination events and paralogous structures in LCR22 regions.

DOI 10.1101/2024.03.14.585046

humanwhole-genome sequencing

𝕏 PostBluesky