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

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

Published:2017-05-19 Issue:1 Volume:10 Page:
ISSN:1755-8794
Container-title:BMC Medical Genomics
language:en
Short-container-title:BMC Med Genomics

Author:

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^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12920-017-0271-4.pdf

Reference21 articles.

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4. Walsh T, Casadei S, Lee MK, Pennil CC, Nord AS, Thornton AM, et al. Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. Proc Natl Acad Sci U S A. 2011;108(44):18032–7. doi: 10.1073/pnas.1115052108 .

5. Walsh T, Lee MK, Casadei S, Thornton AM, Stray SM, Pennil C, et al. Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing. Proc Natl Acad Sci U S A. 2010;107(28):12629–33. doi: 10.1073/pnas.1007983107 .

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