Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

Human genomics

Volumn 9, Issue , 2015, Pages 12-

  Karageorgos, Ioannis ^a   Mizzi, Clint ^a   Giannopoulou, Efstathia ^a   Pavlidis, Cristiana ^a   Peters, Brock A ^a   Zagoriti, Zoi ^b   Stenson, Peter D ^a   Mitropoulos, Konstantinos ^a   Borg, Joseph ^a   Kalofonos, Haralabos P ^a   Drmanac, Radoje ^a   Stubbs, Andrew ^b   van der Spek, Peter ^b   Cooper, David N ^a   Katsila, Theodora ^a   Patrinos, George P ^a  

^a UNIVERSITY OF PATRAS   (Greece)

^b BGI SHENZHEN   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BRCA1 PROTEIN; BRCA1 PROTEIN, HUMAN; DNA BINDING PROTEIN; MLL2 PROTEIN, HUMAN; MSH2 PROTEIN, HUMAN; PROTEIN MSH2; TUMOR PROTEIN;

GENETIC PREDISPOSITION; GENETICS; GENOMICS; HIGH THROUGHPUT SEQUENCING; HUMAN; MUTATION; NEOPLASM; PATHOLOGY; PEDIGREE; PROCEDURES; SINGLE NUCLEOTIDE POLYMORPHISM;

BRCA1 PROTEIN; DNA-BINDING PROTEINS; GENETIC PREDISPOSITION TO DISEASE; GENOMICS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MUTATION; MUTS HOMOLOG 2 PROTEIN; NEOPLASM PROTEINS; NEOPLASMS; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84979866944     PISSN: None     EISSN: 14797364     Source Type: Journal    
DOI: 10.1186/s40246-015-0034-2     Document Type: Article

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