Whole genome sequencing as a means to assess pathogenic mutations in medical genetics and cancer

Cellular and Molecular Life Sciences

Volumn 72, Issue 8, 2015, Pages 1463-1471

  Royer Bertrand, Beryl ^a   Rivolta, Carlo ^a  

^a UNIVERSITY OF LAUSANNE   (Switzerland)

Author keywords

Exome; Hereditary disease; Mutation; Polymorphism

Indexed keywords

DNA SEQUENCE; GENETIC DATABASE; GENETIC DISORDER; GENETIC POLYMORPHISM; GENETICS; GERMLINE MUTATION; HIGH THROUGHPUT SEQUENCING; HUMAN; HUMAN GENOME; MEDICAL GENETICS; NEOPLASM; PATHOLOGY;

DATABASES, GENETIC; GENETIC DISEASES, INBORN; GENETICS, MEDICAL; GENOME, HUMAN; GERM-LINE MUTATION; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; NEOPLASMS; POLYMORPHISM, GENETIC; SEQUENCE ANALYSIS, DNA;

EID: 84925382330     PISSN: 1420682X     EISSN: 14209071     Source Type: Journal    
DOI: 10.1007/s00018-014-1807-9     Document Type: Review

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