A decade of structural variants: Description, history and methods to detect structural variation

Briefings in Functional Genomics

Volumn 14, Issue 5, 2015, Pages 305-314

  Escaramís, Geórgia ^a   Docampo, Elisa ^b   Rabionet, Raquel ^a  

^a Centre for Genomic Regulation   (Spain)

^b UNIVERSITY OF LIÈGE   (Belgium)

Author keywords

Copy number variants; Structural variation

Indexed keywords

ARTICLE; DNA END JOINING REPAIR; GENE FREQUENCY; GENETIC VARIABILITY; GENOMIC INSTABILITY; HIGH THROUGHPUT SEQUENCING; HISTORY OF MEDICINE; HUMAN; INDEL MUTATION; NEXT GENERATION SEQUENCING; NONHUMAN; SINGLE NUCLEOTIDE POLYMORPHISM; VARIABLE NUMBER OF TANDEM REPEAT; DNA SEQUENCE; GENETIC VARIATION; GENETICS; GENOMICS; HISTORY; HUMAN GENOME; PROCEDURES;

GENOME, HUMAN; GENOMIC STRUCTURAL VARIATION; GENOMICS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HISTORY, 20TH CENTURY; HISTORY, 21ST CENTURY; HUMANS; SEQUENCE ANALYSIS, DNA;

EID: 84942323064     PISSN: 20412649     EISSN: 20412657     Source Type: Journal    
DOI: 10.1093/bfgp/elv014     Document Type: Article

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