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 ...
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Dokumenttyp: | Artikel |
Erscheinungsdatum: | 2024 |
Reihe/Periodikum: | International Journal of Neonatal Screening, Vol 10, Iss 1, p 20 (2024) |
Verlag/Hrsg.: |
MDPI AG
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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 |
Powered By: | BASE |
Link(s) : | https://doi.org/10.3390/ijns10010020 |