Author

Anouk C. de Jong

Erasmus MC Cancer InstituteORCID 0000-0002-7381-3171Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:machine learning (classical)· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Chris J. de WitteiD· 1 shared Christina Stangl· 1 shared Ivo Renkens· 1 shared Jean HelmijriD· 1 shared John W.M. MartensiD· 1 shared Jose Espejo Valle-InclániD· 1 shared Lisanne F. van Dessel· 1 shared Markus J. van RoosmaleniD· 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

Chris J. de WitteORCID

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1 paper

Recent·Most cited

Rapid identification of genomic structural variations with nanopore sequencing enables blood-based cancer monitoring

Jose Espejo Valle-Inclán, Christina Stangl, Anouk C. de Jong, Lisanne F. van Dessel, Markus J. van Roosmalen, Jean Helmijr, Ivo Renkens, Roel Janssen, Sam de Blank, Chris J. de Witte, John W.M. Martens, Maurice P.H.M. Jansen, Martijn P. Lolkema, Wigard P. Kloosterman

SHARC rapidly identifies somatic genomic structural variations from nanopore sequencing for blood-based cancer monitoring, detecting ten SVs per sample and enabling treatment response tracking in metastatic prostate cancer.

Genome Medicine · May 18, 2021Peer-reviewedGenetic & Genomic Medicine