Future of Dutch NGS-Based Newborn Screening: Exploring the Technical Possibilities and Assessment of a Variant Classification Strategy

In this study, we compare next-generation sequencing (NGS) approaches (targeted panel (tNGS), whole exome sequencing (WES), and whole genome sequencing (WGS)) for application in newborn screening (NBS). DNA was extracted from dried blood spots (DBS) from 50 patients with genetically confirmed inherited metabolic disorders (IMDs) and 50 control samples. One hundred IMD-related genes were analyzed. Two data-filtering strategies were applied: one to detect only (likely) pathogenic ((L)P) variants, and one to detect (L)P variants in combination with variants of unknown significance (VUS). The vari... Mehr ...

Verfasser: Gea Kiewiet
Dineke Westra
Eddy N. de Boer
Emma van Berkel
Tom G. J. Hofste
Martine van Zweeden
Ronny C. Derks
Nico F. A. Leijsten
Martina H. A. Ruiterkamp-Versteeg
Bart Charbon
Lennart Johansson
Janneke Bos-Kruizinga
Inge J. Veenstra
Monique G. M. de Sain-van der Velden
Els Voorhoeve
M. Rebecca Heiner-Fokkema
Francjan van Spronsen
Birgit Sikkema-Raddatz
Marcel Nelen
Dokumenttyp: Artikel
Erscheinungsdatum: 2024
Reihe/Periodikum: International Journal of Neonatal Screening, Vol 10, Iss 1, p 20 (2024)
Verlag/Hrsg.: MDPI AG
Schlagwörter: newborn screening / next-generation sequencing / inherited metabolic disorder / dried blood spots / Pediatrics / RJ1-570
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-28986959
Datenquelle: BASE; Originalkatalog
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Link(s) : https://doi.org/10.3390/ijns10010020