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Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.
Marioni JC, Thorne NP, Valsesia A, Fitzgerald T, Redon R, Fiegler H, Andrews TD, Stranger BE, Lynch AG, Dermitzakis ET, Carter NP, Tavaré S, Hurles ME
Genome Biol
2007,
8
:R228
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PubMed Central articles that cite the above article:
1.
Runs of homozygosity in European populations.
McQuillan R, Leutenegger AL, Abdel-Rahman R, Franklin CS, Pericic M, Barac-Lauc L, Smolej-Narancic N, Janicijevic B, Polasek O, Tenesa A, Macleod AK, Farrington SM, Rudan P, Hayward C, Vitart V, Rudan I, Wild SH, Dunlop MG, Wright AF, Campbell H, Wilson JF
Am J Hum Genet
2008 Sep,
83
:359-72
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Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms.
Diskin SJ, Li M, Hou C, Yang S, Glessner J, Hakonarson H, Bucan M, Maris JM, Wang K
Nucleic Acids Res
2008 Nov,
36
:e126
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The current excitement about copy-number variation: how it relates to gene duplications and protein families.
Korbel JO, Kim PM, Chen X, Urban AE, Weissman S, Snyder M, Gerstein MB
Curr Opin Struct Biol
2008 Jun,
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A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.
Takeuchi F, McGinnis R, Bourgeois S, Barnes C, Eriksson N, Soranzo N, Whittaker P, Ranganath V, Kumanduri V, McLaren W, Holm L, Lindh J, Rane A, Wadelius M, Deloukas P
PLoS Genet
2009 Mar,
5
:e1000433
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