Performance of high-throughput sequencing for the discovery of genetic variation across the complete size spectrum

G3: Genes, Genomes, Genetics

Volumn 4, Issue 1, 2014, Pages 63-65

  Pang, Andy Wing Chun ^a,b   MacDonald, Jeffrey R ^b   Yuen, Ryan K C ^b   Hayes, Vanessa M ^c   Scherer, Stephen W ^a,b  

^a UNIVERSITY OF TORONTO   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c J CRAIG VENTER INSTITUTE   (United States)

Author keywords

Copy number variation; Genome variation annotation; High throughput sequencing; Insertion deletion

Indexed keywords

REPETITIVE DNA;

ARTICLE; COPY NUMBER VARIATION; GENE DELETION; GENE FREQUENCY; GENE INSERTION; GENETIC VARIABILITY; GENOME; HIGH THROUGHPUT SEQUENCING;

COPY NUMBER VARIATION; GENOME VARIATION ANNOTATION; HIGH-THROUGHPUT SEQUENCING; INSERTION/DELETION;

DNA COPY NUMBER VARIATIONS; GENE DELETION; GENETIC VARIATION; GENOME, HUMAN; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS;

EID: 84892737572     PISSN: None     EISSN: 21601836     Source Type: Journal    
DOI: 10.1534/g3.113.008797     Document Type: Article

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