Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing

BACKGROUND: The growing number of Next Generation Sequencing (NGS) tests is transforming the routine clinical diagnosis of hereditary cancers. Identifying whether a cancer is the result of an underlying disease-causing mutation in a cancer predisposition gene is not only diagnostic for a cancer pred...

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Detalles Bibliográficos
Autores principales: Cheng, Donavan T., Prasad, Meera, Chekaluk, Yvonne, Benayed, Ryma, Sadowska, Justyna, Zehir, Ahmet, Syed, Aijazuddin, Wang, Yan Elsa, Somar, Joshua, Li, Yirong, Yelskaya, Zarina, Wong, Donna, Robson, Mark E., Offit, Kenneth, Berger, Michael F., Nafa, Khedoudja, Ladanyi, Marc, Zhang, Liying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Technical Advance
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437632/
https://www.ncbi.nlm.nih.gov/pubmed/28526081
http://dx.doi.org/10.1186/s12920-017-0271-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437632/
https://www.ncbi.nlm.nih.gov/pubmed/28526081
http://dx.doi.org/10.1186/s12920-017-0271-4

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