Origins and functional impact of copy number variation in the human genome-Reference-Cited by-同舟云学术

Origins and functional impact of copy number variation in the human genome

Published:2009-10-07 Issue:7289 Volume:464 Page:704-712
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Conrad Donald F., ,Pinto Dalila,Redon Richard,Feuk Lars,Gokcumen Omer,Zhang Yujun,Aerts Jan,Andrews T. Daniel,Barnes Chris,Campbell Peter,Fitzgerald Tomas,Hu Min,Ihm Chun Hwa,Kristiansson Kati,MacArthur Daniel G.,MacDonald Jeffrey R.,Onyiah Ifejinelo,Pang Andy Wing Chun,Robson Sam,Stirrups Kathy,Valsesia Armand,Walter Klaudia,Wei John,Tyler-Smith Chris,Carter Nigel P.,Lee Charles,Scherer Stephen W.,Hurles Matthew E.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature08516.pdf

Reference50 articles.

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2. Levy, S. & Strausberg, R. L. Human genetics: Individual genomes diversify. Nature 456, 49–51 (2008)

3. Frazer, K. A. et al. A second generation human haplotype map of over 3.1 million SNPs. Nature 449, 851–861 (2007)

4. Marchini, J. et al. A new multipoint method for genome-wide association studies by imputation of genotypes. Nature Genet. 39, 906–913 (2007)

5. Levy, S. et al. The diploid genome sequence of an individual human. PLoS Biol. 5, e254 (2007)

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