A novel scatterplot-based method to detect copy number variation (CNV)

Objective: Most methods to detect copy number variation (CNV) have high false positive rates, especially for small CNVs and in real-life samples from clinical studies. In this study, we explored a novel scatterplot-based method to detect CNVs in microarray samples. Methods: Illumina SNP microarray d...

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Detalles Bibliográficos
Autores principales: Qiao, Jia-Lu, Levinson, Rebecca T., Chen, Bowang, Engelter, Stefan T., Erhart, Philipp, Gaynor, Brady J., McArdle, Patrick F., Schlicht, Kristina, Krawczak, Michael, Stenman, Martin, Lindgren, Arne G., Cole, John W., Grond-Ginsbach, Caspar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359988/
https://www.ncbi.nlm.nih.gov/pubmed/37485343
http://dx.doi.org/10.3389/fgene.2023.1166972

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