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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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6403216/
https://ncbi.nlm.nih.gov/pubmed/30842562
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-40364-5
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