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  1. Article ; Online: Future of Dutch NGS-Based Newborn Screening: Exploring the Technical Possibilities and Assessment of a Variant Classification Strategy.

    Kiewiet, Gea / Westra, Dineke / de Boer, Eddy N / van Berkel, Emma / Hofste, Tom G J / van Zweeden, Martine / Derks, Ronny C / Leijsten, Nico F A / Ruiterkamp-Versteeg, Martina H A / Charbon, Bart / Johansson, Lennart / Bos-Kruizinga, Janneke / Veenstra, Inge J / de Sain-van der Velden, Monique G M / Voorhoeve, Els / Heiner-Fokkema, M Rebecca / van Spronsen, Francjan / Sikkema-Raddatz, Birgit / Nelen, Marcel

    International journal of neonatal screening

    2024  Volume 10, Issue 1

    Abstract: 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 ...

    Abstract 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 variants were filtered and interpreted, defining true/false positives (TP/FP) and true/false negatives (TN/FN). The variant filtering strategies were assessed in a background cohort (BC) of 4833 individuals. Reliable results were obtained within 5 days. TP results (47 patient samples) for tNGS, WES, and WGS results were 33, 31, and 30, respectively, using the (L)P filtering, and 40, 40, and 38, respectively, when including VUS. FN results were 11, 13, and 14, respectively, excluding VUS, and 4, 4, and 6, when including VUS. The remaining FN were mainly samples with a homozygous VUS. All controls were TN. Three BC individuals showed a homozygous (L)P variant, all related to a variable, mild phenotype. The use of NGS-based workflows in NBS seems promising, although more knowledge of data handling, automated variant interpretation, and costs is needed before implementation.
    Language English
    Publishing date 2024-03-07
    Publishing country Switzerland
    Document type Journal Article
    ISSN 2409-515X
    ISSN (online) 2409-515X
    DOI 10.3390/ijns10010020
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Minigene-Based Splice Assays Reveal the Effect of Non-Canonical Splice Site Variants in

    Reurink, Janine / Oostrik, Jaap / Aben, Marco / Ramos, Mariana Guimarães / van Berkel, Emma / Ołdak, Monika / van Wijk, Erwin / Kremer, Hannie / Roosing, Susanne / Cremers, Frans P M

    International journal of molecular sciences

    2022  Volume 23, Issue 21

    Abstract: Non-canonical splice site variants are increasingly recognized as a relevant cause of ... ...

    Abstract Non-canonical splice site variants are increasingly recognized as a relevant cause of the
    MeSH term(s) Humans ; Usher Syndromes/genetics ; HEK293 Cells ; RNA Precursors ; Extracellular Matrix Proteins/genetics ; Mutation ; RNA Splice Sites/genetics
    Chemical Substances RNA Precursors ; Extracellular Matrix Proteins ; RNA Splice Sites ; USH2A protein, human
    Language English
    Publishing date 2022-11-01
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms232113343
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Scrutinizing pathogenicity of the USH2A c.2276 G > T; p.(Cys759Phe) variant.

    Reurink, Janine / de Vrieze, Erik / Li, Catherina H Z / van Berkel, Emma / Broekman, Sanne / Aben, Marco / Peters, Theo / Oostrik, Jaap / Neveling, Kornelia / Venselaar, Hanka / Ramos, Mariana Guimarães / Gilissen, Christian / Astuti, Galuh D N / Galbany, Jordi Corominas / van Lith-Verhoeven, Janneke J C / Ockeloen, Charlotte W / Haer-Wigman, Lonneke / Hoyng, Carel B / Cremers, Frans P M /
    Kremer, Hannie / Roosing, Susanne / van Wijk, Erwin

    NPJ genomic medicine

    2022  Volume 7, Issue 1, Page(s) 37

    Abstract: The USH2A variant c.2276 G > T (p.(Cys759Phe)) has been described by many authors as a frequent cause of autosomal recessive retinitis pigmentosa (arRP). However, this is in contrast with the description of two asymptomatic individuals homozygous for ... ...

    Abstract The USH2A variant c.2276 G > T (p.(Cys759Phe)) has been described by many authors as a frequent cause of autosomal recessive retinitis pigmentosa (arRP). However, this is in contrast with the description of two asymptomatic individuals homozygous for this variant. We therefore assessed pathogenicity of the USH2A c.2276 G > T variant using extensive genetic and functional analyses. Whole genome sequencing and optical genome mapping were performed for three arRP cases homozygous for USH2A c.2276 G > T to exclude alternative genetic causes. A minigene splice assay was designed to investigate the effect of c.2276 G > T on pre-mRNA splicing, in presence or absence of the nearby c.2256 T > C variant. Moreover, an ush2a
    Language English
    Publishing date 2022-06-07
    Publishing country England
    Document type Journal Article
    ZDB-ID 2813848-X
    ISSN 2056-7944 ; 2056-7944
    ISSN (online) 2056-7944
    ISSN 2056-7944
    DOI 10.1038/s41525-022-00306-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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