Detection of chromosome structural variation by targeted next-generation sequencing and a deep learning application

Molecular testing is increasingly important in cancer diagnosis. Targeted next generation sequencing (NGS) is widely accepted method but structural variation (SV) detection by targeted NGS remains challenging. In the brain tumor, identification of molecular alterations, including 1p/19q co-deletion,...

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Detalles Bibliográficos
Autores principales: Park, Hosub, Chun, Sung-Min, Shim, Jooyong, Oh, Ji-Hye, Cho, Eun Jeong, Hwang, Hee Sang, Lee, Ji-Young, Kim, Deokhoon, Jang, Se Jin, Nam, Soo Jeong, Hwang, Changha, Sohn, Insuk, Sung, Chang Ohk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403216/
https://www.ncbi.nlm.nih.gov/pubmed/30842562
http://dx.doi.org/10.1038/s41598-019-40364-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403216/
https://www.ncbi.nlm.nih.gov/pubmed/30842562
http://dx.doi.org/10.1038/s41598-019-40364-5

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