Genome-wide cell-free DNA screening: a focus on copy-number variants

PURPOSE: Of 86,902 prenatal genome-wide cell-free DNA (cfDNA) screening tests, 4,121 were positive for a chromosome abnormality. This study examines 490 cases screen-positive for one or more subchromosomal copy-number variants (CNV) from genome-wide cfDNA screening. METHODS: Cases positive for one o...

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Detalles Bibliográficos
Autores principales: Rafalko, Jill, Soster, Erica, Caldwell, Samantha, Almasri, Eyad, Westover, Thomas, Weinblatt, Vivian, Cacheris, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486654/
https://www.ncbi.nlm.nih.gov/pubmed/34155363
http://dx.doi.org/10.1038/s41436-021-01227-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486654/
https://www.ncbi.nlm.nih.gov/pubmed/34155363
http://dx.doi.org/10.1038/s41436-021-01227-5

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