A copy number variation map of the human genome

Nature Reviews Genetics

Volumn 16, Issue 3, 2015, Pages 172-183

  Zarrei, Mehdi ^a   MacDonald, Jeffrey R ^a   Merico, Daniele ^a   Scherer, Stephen W ^a,b  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME; COPY NUMBER VARIATION; DIPLOIDY; ETHNICITY; GENE DELETION; GENE DUPLICATION; GENE FUNCTION; GENE MAPPING; GENETIC VARIABILITY; GENOMIC INSTABILITY; HUMAN; HUMAN GENOME; NEXT GENERATION SEQUENCING; PHENOTYPE; PRIORITY JOURNAL; REVIEW; CHROMOSOME MAP; DNA MICROARRAY; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; HIGH THROUGHPUT SEQUENCING;

DNA;

CHROMOSOME MAPPING; DNA; DNA COPY NUMBER VARIATIONS; GENE DELETION; GENE DUPLICATION; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; GENOTYPE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE;

EID: 84923642484     PISSN: 14710056     EISSN: 14710064     Source Type: Journal    
DOI: 10.1038/nrg3871     Document Type: Review

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