Global variation in copy number in the human genome

Nature

Volumn 444, Issue 7118, 2006, Pages 444-454

  Redon, Richard ^a   Ishikawa, Shumpei ^b   Fitch, Karen R ^c   Feuk, Lars ^d,e   Perry, George H ^f   Andrews, T Daniel ^a   Fiegler, Heike ^a   Shapero, Michael H ^c   Carson, Andrew R ^d,e   Chen, Wenwei ^c   Cho, Eun Kyung ^f   Dallaire, Stephanie ^f   Freeman, Jennifer L ^f   González, Juan R ^g   Gratacòs, Mònica ^g   Huang, Jing ^c   Kalaitzopoulos, Dimitrios ^a   Komura, Daisuke ^b   MacDonald, Jeffrey R ^d   Marshall, Christian R ^d,e   Mei, Rui ^c   Montgomery, Lyndal ^a   Nishimura, Kunihiro ^b   Okamura, Kohji ^d,e   Shen, Fan ^c   Somerville, Martin J ^h   Tchinda, Joelle ^f   Valsesia, Armand ^a   Woodwark, Cara ^a   Yang, Fengtang ^a   Zhang, Junjun ^d   Zerjal, Tatiana ^a   Zhang, Jane ^c   Armengol, Lluis ^g   Conrad, Donald F ⁱ   Estivill, Xavier ^g,j   Tyler Smith, Chris ^a   Carter, Nigel P ^a   Aburatani, Hiroyuki ^b,k   Lee, Charles ^f,l   Jones, Keith W ^c   Scherer, Stephen W ^d,e   Hurles, Matthew E ^a   more..

^a WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^b UNIVERSITY OF TOKYO   (Japan)

^c Thermo Fisher Scientific   (United States)

^d HOSPITAL FOR SICK CHILDREN   (Canada)

^e UNIVERSITY OF TORONTO   (Canada)

^f BRIGHAM AND WOMEN S HOSPITAL   (United States)

^g Barcelona Biomedical Research Park   (Spain)

^h UNIVERSITY OF ALBERTA   (Canada)

ⁱ UNIVERSITY OF CHICAGO   (United States)

^j UNIVERSITAT POMPEU FABRA   (Spain)

^k JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^l HARVARD MEDICAL SCHOOL   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARRAYS; DATA ACQUISITION; DISEASES; DNA SEQUENCES; GENES; NUCLEIC ACIDS; POPULATION STATISTICS;

COPY NUMBER VARIATION (CNV); GENETIC DISEASE; HUMAN GENOME; SINGLE NUCLEOTIDE POLYMORPHISM (SNP);

GENETIC ENGINEERING;

ANDROGEN; BETA CRYSTALLIN; CHEMOKINE; DNA; GLUCURONOSYLTRANSFERASE;

DNA; GENETIC ANALYSIS; GENETIC VARIATION; GENOME; GEOGRAPHICAL VARIATION; POPULATION GENETICS;

AFRICA; ALU SEQUENCE; ARTICLE; ASIA; BTNL2 GENE; CCL3L1 GENE; CHROMOSOME ABERRATION; COMPARATIVE GENOMIC HYBRIDIZATION; CRYBB2 GENE; CRYBB3 GENE; DIGEORGE SYNDROME; EUROPE; EVOLUTION; FCGR3B GENE; GENE; GENE DELETION; GENE DUPLICATION; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENETIC VARIABILITY; GENOTYPE; HAPPY PUPPET SYNDROME; HERITABILITY; HOMOLOGOUS RECOMBINATION; HUMAN; HUMAN GENOME; MAPT GENE; POPULATION GENETICS; PRADER WILLI SYNDROME; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM; SMITH MAGENIS SYNDROME; UGT2B17 GENE; WILLIAMS BEUREN SYNDROME;

CHROMOSOME MAPPING; GENE DOSAGE; GENETICS, POPULATION; GENOME, HUMAN; GENOMICS; GENOTYPE; HUMANS; LINKAGE DISEQUILIBRIUM; MOLECULAR DIAGNOSTIC TECHNIQUES; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; VARIATION (GENETICS);

AFRICA; ASIA; EURASIA; EUROPE;

EID: 33751329250     PISSN: 00280836     EISSN: 14764679     Source Type: Journal    
DOI: 10.1038/nature05329     Document Type: Article

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