Author

Ed M. D. Schuuring

University Medical Center GroningenORCID 0000-0003-3655-143XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Andries De KokeriD· 1 shared Anxhela ZakaiD· 1 shared Bastiaan B.J. TopsiD· 1 shared Björn MenteniD· 1 shared Bram De WildeiD· 1 shared Bram Van GaeveriD· 1 shared Clémence T. B. Pasmans· 1 shared Edwin P. J. G. CuppeniD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenomics

Andries De KokerORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintSep 8, 2025

Development of circulating cell-free DNA reduced representation bisulfite sequencing for clinical methylomics diagnostics

Andries De Koker, Lennart Raman, Ruben Van Paemel…·Nico Callewaert

The paper introduces cf-RRBS, a method for methylation profiling of fragmented plasma DNA, enabling cost-effective and accurate non-invasive lung cancer subtyping.

24 citations

DNA methylationexperimental assay

𝕏 PostBluesky

Genetic & Genomic MedicineExpert Review of Pharmacoeconomics & Outcomes ResearchPeer-reviewedApr 15, 2021

Micro-costing Diagnostics in Oncology: From Single-Gene Testing to Whole Genome Sequencing

Clémence T. B. Pasmans, Bastiaan B.J. Tops, Elisabeth M. P. Steeghs…·Geert Frederix

This study compares the costs of various diagnostic techniques, including whole genome sequencing, for treating specific cancers in the Netherlands.

42 citationstop 4%

whole-genome sequencingstatistical model

𝕏 PostBluesky