1:
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(10):R228.
PMID: 17961237 [PubMed - indexed for MEDLINE]
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3:
The fine-scale and complex architecture of human copy-number variation.
Perry GH, Ben-Dor A, Tsalenko A, Sampas N, Rodriguez-Revenga L, Tran CW, Scheffer A, Steinfeld I, Tsang P, Yamada NA, Park HS, Kim JI, Seo JS, Yakhini Z, Laderman S, Bruhn L, Lee C.
Am J Hum Genet. 2008 Mar;82(3):685-95. Epub 2008 Jan 24.
PMID: 18304495 [PubMed - indexed for MEDLINE]
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6:
Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data.
Baross A, Delaney AD, Li HI, Nayar T, Flibotte S, Qian H, Chan SY, Asano J, Ally A, Cao M, Birch P, Brown-John M, Fernandes N, Go A, Kennedy G, Langlois S, Eydoux P, Friedman JM, Marra MA.
BMC Bioinformatics. 2007 Oct 2;8:368.
PMID: 17910767 [PubMed - indexed for MEDLINE]
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7:
A high-resolution map of segmental DNA copy number variation in the mouse genome.
Graubert TA, Cahan P, Edwin D, Selzer RR, Richmond TA, Eis PS, Shannon WD, Li X, McLeod HL, Cheverud JM, Ley TJ.
PLoS Genet. 2007 Jan 5;3(1):e3. Epub 2006 Nov 22.
PMID: 17206864 [PubMed - indexed for MEDLINE]
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9:
Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes.
Shen F, Huang J, Fitch KR, Truong VB, Kirby A, Chen W, Zhang J, Liu G, McCarroll SA, Jones KW, Shapero MH.
BMC Genet. 2008 Mar 28;9:27.
PMID: 18373861 [PubMed - indexed for MEDLINE]
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10:
Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array.
de Ståhl TD, Sandgren J, Piotrowski A, Nord H, Andersson R, Menzel U, Bogdan A, Thuresson AC, Poplawski A, von Tell D, Hansson CM, Elshafie AI, Elghazali G, Imreh S, Nordenskjöld M, Upadhyaya M, Komorowski J, Bruder CE, Dumanski JP.
Hum Mutat. 2008 Mar;29(3):398-408.
PMID: 18058796 [PubMed - indexed for MEDLINE]
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11:
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.
Komura D, Shen F, Ishikawa S, Fitch KR, Chen W, Zhang J, Liu G, Ihara S, Nakamura H, Hurles ME, Lee C, Scherer SW, Jones KW, Shapero MH, Huang J, Aburatani H.
Genome Res. 2006 Dec;16(12):1575-84. Epub 2006 Nov 22.
PMID: 17122084 [PubMed - indexed for MEDLINE]
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12:
Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome.
Korbel JO, Urban AE, Grubert F, Du J, Royce TE, Starr P, Zhong G, Emanuel BS, Weissman SM, Snyder M, Gerstein MB.
Proc Natl Acad Sci U S A. 2007 Jun 12;104(24):10110-5. Epub 2007 Jun 5.
PMID: 17551006 [PubMed - indexed for MEDLINE]
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17:
X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation.
Madrigal I, Rodríguez-Revenga L, Armengol L, González E, Rodriguez B, Badenas C, Sánchez A, Martínez F, Guitart M, Fernández I, Arranz JA, Tejada M, Pérez-Jurado LA, Estivill X, Milà M.
BMC Genomics. 2007 Nov 29;8:443.
PMID: 18047645 [PubMed - indexed for MEDLINE]
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19:
Accurate and reliable high-throughput detection of copy number variation in the human genome.
Fiegler H, Redon R, Andrews D, Scott C, Andrews R, Carder C, Clark R, Dovey O, Ellis P, Feuk L, French L, Hunt P, Kalaitzopoulos D, Larkin J, Montgomery L, Perry GH, Plumb BW, Porter K, Rigby RE, Rigler D, Valsesia A, Langford C, Humphray SJ, Scherer SW, Lee C, Hurles ME, Carter NP.
Genome Res. 2006 Dec;16(12):1566-74. Epub 2006 Nov 22.
PMID: 17122085 [PubMed - indexed for MEDLINE]
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