Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid...
Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing
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Author / Creator
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 and Zhang, Liying
Publisher
England: BioMed Central
Journal title
Language
English
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Publication information
Publisher
England: BioMed Central
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Scope and Contents
Contents
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 predisposition syndrome, but also has significant clinical implica...
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Full title
Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing
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Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_972eab9f9a884f718c0b98031b307246
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_972eab9f9a884f718c0b98031b307246
Other Identifiers
ISSN
1755-8794
E-ISSN
1755-8794
DOI
10.1186/s12920-017-0271-4
