Validation of Customized Cancer Panel for Detecting Somatic Mutations and Copy Number Alterations

Accurate detection of genomic alterations, especially druggable hotspot mutations in tumors, has become an essential part of precision medicine. With targeted sequencing, we can obtain deeper coverage of reads and handle data more easily with a relatively lower cost and less time than whole-exome or...

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Detalles Bibliográficos
Autores principales: Choi, Su-Hye, Jung, Seung-Hyun, Chung, Yeun-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Gastrointestinal Intervention 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769856/
https://www.ncbi.nlm.nih.gov/pubmed/29307139
http://dx.doi.org/10.5808/GI.2017.15.4.136

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769856/
https://www.ncbi.nlm.nih.gov/pubmed/29307139
http://dx.doi.org/10.5808/GI.2017.15.4.136

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