Author

Geert Vandeweyer

University of AntwerpORCID 0000-0002-6262-6522Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Joris Robert VermeeschiD· 2 shared Aimé Zola LumakaiD· 1 shared Amin ArdeshirdavaniiD· 1 shared Annelies DheedeneiD· 1 shared Baroni Maria Chiara· 1 shared Benjamin HuremagiciD· 1 shared Beyltjens Tessi· 1 shared Björn MenteniD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Joris Robert VermeeschORCID

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2 papers

Recent·Most cited

A nationwide prospective randomized trial for diagnosing developmental disorders demonstrates genome sequencing outperforms standard of care.

Mathilde Geysens, Erika L. Souche, Baroni Maria Chiara, Valérie Benoît, Beyltjens Tessi, Wouter Bossuyt, Vincent Bours, Marian Crabbe, Croes Didier, De Smet Matthias, Julie Désir, Koenraad Devriendt, Annelies Dheedene, Dimitrov Boyan Ivanov, Katrien Janssens, , Joris Robert Vermeesch

A randomized trial compares genome sequencing to standard of care in diagnosing developmental disorders, finding higher diagnostic yield with genome sequencing.

medRxiv · Oct 18, 2025 · PreprintGenetic & Genomic Medicine

WiNGS: Widely integrated NGS platform for federated genome analysis

Haleh Chizari, Nishkala Sattanathan, Amin Ardeshirdavani, Nasim Shabani, Benjamin Huremagic, Joris Robert Vermeesch, Yves Moreau, Geert Vandeweyer

WiNGS enables federated analysis of omics data across a consortium without centralized storage, supporting variant interpretation for rare disease diagnosis.

bioRxiv · Jun 23, 2022 · PreprintBioinformatics