Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations.

Sprissler, Ryan; Perkins, Bryce; Johnstone, Laurel; Babiker, Hani M; Chalasani, Pavani; Lau, Branden; Hammer, Michael; Mahadevan, Daruka

Sprissler, Ryan; Perkins, Bryce; Johnstone, Laurel; Babiker, Hani M; Chalasani, Pavani; Lau, Branden; Hammer, Michael; Mahadevan, Daruka.

Afiliación

Sprissler R; Department of Health Sciences, Center for Applied Genetics and Genomic Medicine, University of Arizona, Tucson, AZ 85721, USA.
Perkins B; Arizona Research Labs, University of Arizona Genetics Core, University of Arizona, Tucson, AZ 85721, USA.
Johnstone L; Department of Medicine, Division of Hematology and Oncology, University of Arizona Cancer Center, University of Arizona, Tucson, AZ 85724, USA.
Babiker HM; Arizona Research Labs, University of Arizona Genetics Core, University of Arizona, Tucson, AZ 85721, USA.
Chalasani P; Department of Medicine, Division of Hematology and Oncology, University of Arizona Cancer Center, University of Arizona, Tucson, AZ 85724, USA.
Lau B; Department of Medicine-Hematology/Oncology, University of Texas Health San Antonio, Mays Cancer Center, San Antonio, TX 78229, USA.
Hammer M; Department of Medicine, Division of Hematology and Oncology, University of Arizona Cancer Center, University of Arizona, Tucson, AZ 85724, USA.
Mahadevan D; Department of Medicine-Hematology/Oncology, University of Texas Health San Antonio, Mays Cancer Center, San Antonio, TX 78229, USA.

Cancers (Basel) ; 12(6)2020 Jun 18.

Article en En | MEDLINE | ID: mdl-32570879

Palabras clave

copy number alteration (CNA); double hits; inherited variants; rare tumors; tumor-germline matched sequencing; whole exome sequencing

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Cancers (Basel) Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

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