Mapping and sequencing of structural variation from eight human genomes
Jeffrey M. Kidd(Howard Hughes Medical Institute), Gregory M. Cooper(Howard Hughes Medical Institute), William F. Donahue, Hillary S. Hayden(University of Washington), Nick Sampas(Agilent Technologies (United States)), Tina Graves(Washington University in St. Louis), Nancy F. Hansen(National Institutes of Health), Brian Teague(University of Wisconsin–Madison), Can Alkan(Howard Hughes Medical Institute), Francesca Antonacci(Howard Hughes Medical Institute), Eric Haugen(University of Washington), Troy Zerr(Howard Hughes Medical Institute), N. Alice Yamada(Agilent Technologies (United States)), Peter Tsang(Agilent Technologies (United States)), Tera L. Newman(Howard Hughes Medical Institute), Eray Tüzün(Howard Hughes Medical Institute), Ze Cheng(Howard Hughes Medical Institute), Heather Ebling, Nadeem Tusneem, Robert David, Will Gillett(University of Washington), Karen A. Phelps(University of Washington), Molly Weaver(Howard Hughes Medical Institute), David J. Saranga, Adrianne B. Brand, Wei Tao, Erik Gustafson, Kevin McKernan, Lin Chen(Howard Hughes Medical Institute), Maika Malig(Howard Hughes Medical Institute), Joshua D. Smith(Howard Hughes Medical Institute), Joshua M. Korn(Broad Institute), Steven A. McCarroll(Broad Institute), David A. Altshuler(Broad Institute), Daniel A. Peiffer(Illumina (United States)), Michael O. Dorschner(Howard Hughes Medical Institute), J Stamatoyannopoulos(Howard Hughes Medical Institute), David A. Schwartz(University of Wisconsin–Madison), Deborah A. Nickerson(Howard Hughes Medical Institute), James C. Mullikin(National Institutes of Health), Richard K. Wilson(Washington University in St. Louis), Laurakay Bruhn(Agilent Technologies (United States)), Maynard V. Olson(University of Washington), Rajinder Kaul(University of Washington), Douglas R. Smith, Evan E. Eichler(Howard Hughes Medical Institute)
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Abstract
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