Comparison of Next-Generation Sequencing and Fluorescence In Situ Hybridization for Detection of Segmental Chromosomal Aberrations in Neuroblastoma

The aim of this study was to compare next-generation sequencing (NGS) with the traditional fluorescence in situ hybridization (FISH) for detecting segmental chromosomal aberrations (SCAs) such as 1p deletion, 11q deletion and 17q gain, which are well-known predictive markers for adverse outcome in n...

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Detalles Bibliográficos
Autores principales: Kim, Eojin, Lee, Boram, Lee, Ji Won, Sung, Ki Woong, Kim, Jung-Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465051/
https://www.ncbi.nlm.nih.gov/pubmed/34574043
http://dx.doi.org/10.3390/diagnostics11091702

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465051/
https://www.ncbi.nlm.nih.gov/pubmed/34574043
http://dx.doi.org/10.3390/diagnostics11091702

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