Global variation in copy number in the human genome

Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully ascertained. We have constructed a first-generation CNV map of the human genome through the study of 270 individuals from four populations with ancestry in Europe, Africa or Asia (the HapMap collection)....

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Veröffentlicht in:	Nature 2006-11, Vol.444 (7118), p.444-454
Hauptverfasser:	Redon, Richard, Ishikawa, Shumpei, Fitch, Karen R., Feuk, Lars, Perry, George H., Andrews, T. Daniel, Fiegler, Heike, Shapero, Michael H., Carson, Andrew R., Chen, Wenwei, Cho, Eun Kyung, Dallaire, Stephanie, Freeman, Jennifer L., González, Juan R., Gratacòs, Mònica, Huang, Jing, Kalaitzopoulos, Dimitrios, Komura, Daisuke, MacDonald, Jeffrey R., Marshall, Christian R., Mei, Rui, Montgomery, Lyndal, Nishimura, Kunihiro, Okamura, Kohji, Shen, Fan, Somerville, Martin J., Tchinda, Joelle, Valsesia, Armand, Woodwark, Cara, Yang, Fengtang, Zhang, Junjun, Zerjal, Tatiana, Zhang, Jane, Armengol, Lluis, Conrad, Donald F., Estivill, Xavier, Tyler-Smith, Chris, Carter, Nigel P., Aburatani, Hiroyuki, Lee, Charles, Jones, Keith W., Scherer, Stephen W., Hurles, Matthew E.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Biological variation Chromosome Mapping Deoxyribonucleic acid DNA Fundamental and applied biological sciences. Psychology Gene Dosage Genes. Genome Genetic diversity Genetic resources Genetic Variation Genetics Genetics, Population Genome, Human Genomics Genomics - methods Genotype Genotype & phenotype Human genetics Humanities and Social Sciences Humans Hybridization Life Sciences Linkage Disequilibrium Molecular and cellular biology Molecular Diagnostic Techniques Molecular genetics multidisciplinary Oligonucleotide Array Sequence Analysis - methods Polymorphism, Single Nucleotide Science Science (multidisciplinary)
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