Publications by authors named "Roy Straver"

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Direct detection of 8-oxo-dG using nanopore sequencing.
Marc Pagès-Gallego, Daan M K van Soest, Nicolle J M Besselink, Roy Straver, Janneke P Keijer

Nat Commun· June 2025

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ReQuant: improved base modification calling by k-mer value imputation.
Roy Straver, Carlo Vermeulen, Joe R Verity-Legg, Marc Pagès-Gallego, Dieter G G Stoker

Nucleic Acids Res· May 2025

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Author Correction: Accurate detection of circulating tumor DNA using nanopore consensus sequencing.
Alessio Marcozzi, Myrthe Jager, Martin Elferink, Roy Straver, Joost H van Ginkel

NPJ Genom Med· June 2023

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Accurate detection of circulating tumor DNA using nanopore consensus sequencing.
Alessio Marcozzi, Myrthe Jager, Martin Elferink, Roy Straver, Joost H van Ginkel

NPJ Genom Med· December 2021

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Comprehensive multiparameter genetic analysis improves circulating tumor DNA detection in head and neck cancer patients.
Steven W Mes, Arjen Brink, Erik A Sistermans, Roy Straver, Cees B M Oudejans

Oral Oncol· October 2020

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Multi-contact 4C: long-molecule sequencing of complex proximity ligation products to uncover local cooperative and competitive chromatin topologies.
Carlo Vermeulen, Amin Allahyar, Britta A M Bouwman, Peter H L Krijger, Marjon J A M Verstegen, Roy Straver

Nat Protoc· February 2020

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TargetClone: A multi-sample approach for reconstructing subclonal evolution of tumors.
Marleen M Nieboer, Lambert C J Dorssers, Roy Straver, Leendert H J Looijenga, Jeroen de Ridder

PLoS One· April 2019

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Mosaic maternal 10qter deletions are associated with FRA10B expansions and may cause false-positive noninvasive prenatal screening results.
Karin Huijsdens-van Amsterdam, Roy Straver, Merel C van Maarle, Alida C Knegt, Diane Van Opstal

Genet Med· November 2018

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Enhancer hubs and loop collisions identified from single-allele topologies.
Amin Allahyar, Carlo Vermeulen, Britta A M Bouwman, Peter H L Krijger, Marjon J A M Verstegen, Roy Straver

Nat Genet· August 2018

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Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study.
Diane Van Opstal, Merel C van Maarle, Klaske Lichtenbelt, Marjan M Weiss, Heleen Schuring-Blom, Roy Straver

Genet Med· April 2018

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WISExome: a within-sample comparison approach to detect copy number variations in whole exome sequencing data.
Roy Straver, Marjan M Weiss, Quinten Waisfisz, Erik A Sistermans, Marcel J T Reinders

Eur J Hum Genet· December 2017

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Response to letter to the editor PD-17-0390, a comment on "Comparing methods for fetal fraction determination and quality control of NIPT samples".
Daphne M van Beek, Roy Straver, Marjan M Weiss, Elles M J Boon, Karin Huijsdens-van Amsterdam

Prenat Diagn· December 2017

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Comparing methods for fetal fraction determination and quality control of NIPT samples.
Daphne M van Beek, Roy Straver, Marian M Weiss, Elles M J Boon, Karin Huijsdens-van Amsterdam

Prenat Diagn· August 2017

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Calculating the fetal fraction for noninvasive prenatal testing based on genome-wide nucleosome profiles.
Roy Straver, Cees B M Oudejans, Erik A Sistermans, Marcel J T Reinders

Prenat Diagn· July 2016

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Maternal Malignancies Detected With Noninvasive Prenatal Testing.
Erik Sistermans, Roy Straver, Brigitte H W Faas

JAMA· November 2015

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Introducing WISECONDOR for noninvasive prenatal diagnostics.
Roy Straver, Erik A Sistermans, Marcel J T Reinders

Expert Rev Mol Diagn· June 2014

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WISECONDOR: detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme.
Roy Straver, Erik A Sistermans, Henne Holstege, Allerdien Visser, Cees B M Oudejans

Nucleic Acids Res· March 2014

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