Author

Lieke Schoenmaker

Hartwig Medical FoundationORCID 0000-0003-3609-9869Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alexander HoischeniD· 1 shared Bauke YlstraiD· 1 shared Edwin P. J. G. CuppeniD· 1 shared Ewart de BruijniD· 1 shared Floris H. GroenendijkiD· 1 shared Hendrikus Jan DubbinkiD· 1 shared Jacobus J. M. van der HoeveniD· 1 shared Kim MonkhorstiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexander HoischenORCID

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Author profile →

1 paper

Recent·Most cited

Clinical validation of Whole Genome Sequencing for cancer diagnostics

Paul Roepman, Ewart de Bruijn, Stef van Lieshout, Lieke Schoenmaker, Mirjam C. Boelens, Hendrikus Jan Dubbink, Willemina R.R. Geurts-Giele, Floris H. Groenendijk, Manon M. H. Huibers, Mariëtte E.G. Kranendonk, Margaretha G.M. Roemer, Kris G. Samsom, Marloes Steehouwer, Wendy W.J. de Leng, Alexander Hoischen, , Edwin P. J. G. Cuppen

This study validates whole genome sequencing as a reliable single assay for detecting various cancer mutations with high sensitivity and precision.

Journal of Molecular Diagnostics · May 6, 2021Peer-reviewedGenetic & Genomic Medicine