{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,2]],"date-time":"2026-04-02T02:53:02Z","timestamp":1775098382641,"version":"3.50.1"},"reference-count":24,"publisher":"Oxford University Press (OUP)","issue":"13","license":[{"start":{"date-parts":[[2016,11,7]],"date-time":"2016-11-07T00:00:00Z","timestamp":1478476800000},"content-version":"vor","delay-in-days":3065,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/2.0\/uk\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2008,8]]},"DOI":"10.1093\/nar\/gkn378","type":"journal-article","created":{"date-parts":[[2008,6,18]],"date-time":"2008-06-18T00:24:22Z","timestamp":1213748662000},"page":"e80-e80","source":"Crossref","is-referenced-by-count":70,"title":["Impact of whole genome amplification on analysis of copy number variants"],"prefix":"10.1093","volume":"36","author":[{"given":"T. J.","family":"Pugh","sequence":"first","affiliation":[]},{"given":"A. D.","family":"Delaney","sequence":"additional","affiliation":[]},{"given":"N.","family":"Farnoud","sequence":"additional","affiliation":[]},{"given":"S.","family":"Flibotte","sequence":"additional","affiliation":[]},{"given":"M.","family":"Griffith","sequence":"additional","affiliation":[]},{"given":"H. I.","family":"Li","sequence":"additional","affiliation":[]},{"given":"H.","family":"Qian","sequence":"additional","affiliation":[]},{"given":"P.","family":"Farinha","sequence":"additional","affiliation":[]},{"given":"R. D.","family":"Gascoyne","sequence":"additional","affiliation":[]},{"given":"M. A.","family":"Marra","sequence":"additional","affiliation":[]}],"member":"286","published-online":{"date-parts":[[2008,6,17]]},"reference":[{"key":"key\n\t\t\t\t20170510131148_B1","doi-asserted-by":"crossref","first-page":"86","DOI":"10.1038\/ng1696","article-title":"Common deletion polymorphisms in the human genome","volume":"38","author":"McCarroll","year":"2006","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170510131148_B2","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1038\/nrg1767","article-title":"Structural variation in the human genome","volume":"7","author":"Feuk","year":"2006","journal-title":"Nat. Rev. Genet."},{"key":"key\n\t\t\t\t20170510131148_B3","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1038\/ng1697","article-title":"A high-resolution survey of deletion polymorphism in the human genome","volume":"38","author":"Conrad","year":"2006","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170510131148_B4","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1086\/431652","article-title":"Segmental duplications and copy-number variation in the human genome","volume":"77","author":"Sharp","year":"2005","journal-title":"Am. J. Hum. Genet."},{"key":"key\n\t\t\t\t20170510131148_B5","doi-asserted-by":"crossref","first-page":"949","DOI":"10.1038\/ng1416","article-title":"Detection of large-scale variation in the human genome","volume":"36","author":"Iafrate","year":"2004","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170510131148_B6","doi-asserted-by":"crossref","first-page":"525","DOI":"10.1126\/science.1098918","article-title":"Large-scale copy number polymorphism in the human genome","volume":"305","author":"Sebat","year":"2004","journal-title":"Science"},{"key":"key\n\t\t\t\t20170510131148_B7","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1038\/ng1718","article-title":"APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy","volume":"38","author":"Rovelet-Lecrux","year":"2006","journal-title":"Nat. Genet."},{"key":"key\n\t\t\t\t20170510131148_B8","doi-asserted-by":"crossref","first-page":"312","DOI":"10.1086\/427762","article-title":"High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization","volume":"76","author":"Zhang","year":"2005","journal-title":"Am. J. Hum. Genet."},{"key":"key\n\t\t\t\t20170510131148_B9","doi-asserted-by":"crossref","first-page":"500","DOI":"10.1086\/507471","article-title":"Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation","volume":"79","author":"Friedman","year":"2006","journal-title":"Am. J. Hum. Genet."},{"key":"key\n\t\t\t\t20170510131148_B10","doi-asserted-by":"crossref","first-page":"9625","DOI":"10.1073\/pnas.0504126102","article-title":"High-resolution genomic profiles of human lung cancer","volume":"102","author":"Tonon","year":"2005","journal-title":"Proc. Natl Acad. Sci. USA"},{"key":"key\n\t\t\t\t20170510131148_B11","doi-asserted-by":"crossref","first-page":"3060","DOI":"10.1158\/0008-5472.CAN-03-3308","article-title":"An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays","volume":"64","author":"Zhao","year":"2004","journal-title":"Cancer Res."},{"key":"key\n\t\t\t\t20170510131148_B12","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1016\/j.pbiomolbio.2004.01.007","article-title":"The use of whole genome amplification in the study of human disease","volume":"88","author":"Hughes","year":"2005","journal-title":"Prog. Biophys. Mol. Biol."},{"key":"key\n\t\t\t\t20170510131148_B13","doi-asserted-by":"crossref","first-page":"5261","DOI":"10.1073\/pnas.082089499","article-title":"Comprehensive human genome amplification using multiple displacement amplification","volume":"99","author":"Dean","year":"2002","journal-title":"Proc. Natl Acad. Sci. USA"},{"key":"key\n\t\t\t\t20170510131148_B14","doi-asserted-by":"crossref","first-page":"1965","DOI":"10.1038\/nprot.2006.326","article-title":"Whole-genome multiple displacement amplification from single cells","volume":"1","author":"Spits","year":"2006","journal-title":"Nat. Protoc."},{"key":"key\n\t\t\t\t20170510131148_B15","doi-asserted-by":"crossref","first-page":"77","DOI":"10.2144\/000112308","article-title":"SNP-based chromosomal copy number ascertainment following multiple displacement whole-genome amplification","volume":"42","author":"Corneveaux","year":"2007","journal-title":"Biotechniques"},{"key":"key\n\t\t\t\t20170510131148_B16","doi-asserted-by":"crossref","first-page":"e71","DOI":"10.1093\/nar\/gnh069","article-title":"Genome coverage and sequence fidelity of phi29 polymerase-based multiple strand displacement whole genome amplification","volume":"32","author":"Paez","year":"2004","journal-title":"Nucleic Acids Res."},{"key":"key\n\t\t\t\t20170510131148_B17","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1038\/labinvest.3700495","article-title":"Evaluation of Phi29-based whole-genome amplification for microarray-based comparative genomic hybridisation","volume":"87","author":"Arriola","year":"2007","journal-title":"Lab. Invest."},{"key":"key\n\t\t\t\t20170510131148_B18","doi-asserted-by":"crossref","first-page":"294","DOI":"10.1101\/gr.377203","article-title":"Whole genome analysis of genetic alterations in small DNA samples using hyperbranched strand displacement amplification and array-CGH","volume":"13","author":"Lage","year":"2003","journal-title":"Genome Res."},{"key":"key\n\t\t\t\t20170510131148_B19","doi-asserted-by":"crossref","first-page":"710","DOI":"10.1002\/elps.200410121","article-title":"Genome-wide single-nucleotide polymorphism arrays demonstrate high fidelity of multiple displacement-based whole-genome amplification","volume":"26","author":"Tzvetkov","year":"2005","journal-title":"Electrophoresis"},{"key":"key\n\t\t\t\t20170510131148_B20","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1016\/S1525-1578(10)60543-0","article-title":"Amplification of whole tumor genomes and gene-by-gene mapping of genomic aberrations from limited sources of fresh-frozen and paraffin-embedded DNA","volume":"7","author":"Bredel","year":"2005","journal-title":"J. Mol. Diagn."},{"key":"key\n\t\t\t\t20170510131148_B21","doi-asserted-by":"crossref","first-page":"2719","DOI":"10.1016\/S0021-9258(18)53833-3","article-title":"Fidelity of phi 29 DNA polymerase. Comparison between protein-primed initiation and DNA polymerization","volume":"268","author":"Esteban","year":"1993","journal-title":"J. Biol. Chem."},{"key":"key\n\t\t\t\t20170510131148_B22","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1186\/1471-2164-7-216","article-title":"Assessment of whole genome amplification-induced bias through high-throughput, massively parallel whole genome sequencing","volume":"7","author":"Pinard","year":"2006","journal-title":"BMC Genomics"},{"key":"key\n\t\t\t\t20170510131148_B23","doi-asserted-by":"crossref","first-page":"573","DOI":"10.1093\/nar\/27.2.573","article-title":"Tandem repeats finder: a program to analyze DNA sequences","volume":"27","author":"Benson","year":"1999","journal-title":"Nucleic Acids Res."},{"key":"key\n\t\t\t\t20170510131148_B24","article-title":"BRLMM: an improved genotype calling method for the GeneChip Human Mapping 500K Array Set","volume-title":"Technical Report","author":"Affymetrix","year":"2006"}],"container-title":["Nucleic Acids Research"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/academic.oup.com\/nar\/article-pdf\/36\/13\/e80\/16747513\/gkn378.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,9,12]],"date-time":"2021-09-12T06:24:07Z","timestamp":1631427847000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/nar\/article-lookup\/doi\/10.1093\/nar\/gkn378"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,6,17]]},"references-count":24,"journal-issue":{"issue":"13","published-online":{"date-parts":[[2008,6,17]]},"published-print":{"date-parts":[[2008,8]]}},"URL":"https:\/\/doi.org\/10.1093\/nar\/gkn378","relation":{},"ISSN":["1362-4962","0305-1048"],"issn-type":[{"value":"1362-4962","type":"electronic"},{"value":"0305-1048","type":"print"}],"subject":[],"published":{"date-parts":[[2008,6,17]]}}}