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    Results: 1 to 20 of 234

    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]
    Free PMC Article
    2.

    Large scale copy number variation (CNV) at 14q12 is associated with the presence of genomic abnormalities in neoplasia.

    Braude I, Vukovic B, Prasad M, Marrano P, Turley S, Barber D, Zielenska M, Squire JA.

    BMC Genomics. 2006 Jun 6;7:138.

    PMID:
    16756668
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    Human copy number polymorphic genes.

    Bailey JA, Kidd JM, Eichler EE.

    Cytogenet Genome Res. 2008;123(1-4):234-43. Epub 2009 Mar 11.

    PMID:
    19287160
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    4.

    Hidden copy number variation in the HapMap population.

    Marioni JC, White M, Tavaré S, Lynch AG.

    Proc Natl Acad Sci U S A. 2008 Jul 22;105(29):10067-72. Epub 2008 Jul 15.

    PMID:
    18632583
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    5.

    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]
    Free PMC Article
    6.

    CNV-seq, a new method to detect copy number variation using high-throughput sequencing.

    Xie C, Tammi MT.

    BMC Bioinformatics. 2009 Mar 6;10:80.

    PMID:
    19267900
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    7.

    Segmental copy-number variation observed in Japanese by array-CGH.

    Takahashi N, Tsuyama N, Sasaki K, Kodaira M, Satoh Y, Kodama Y, Sugita K, Katayama H.

    Ann Hum Genet. 2008 Mar;72(Pt 2):193-204. Epub 2008 Jan 20.

    PMID:
    18205891
    [PubMed - indexed for MEDLINE]
    8.

    Identification of recurrent regions of Copy-Number Variants across multiple individuals.

    Mei TS, Salim A, Calza S, Seng KC, Seng CK, Pawitan Y.

    BMC Bioinformatics. 2010 Mar 22;11:147.

    PMID:
    20307285
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    9.

    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]
    Free PMC Article
    10.

    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]
    Free PMC Article
    11.

    CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics.

    Gai X, Perin JC, Murphy K, O'Hara R, D'arcy M, Wenocur A, Xie HM, Rappaport EF, Shaikh TH, White PS.

    BMC Bioinformatics. 2010 Feb 4;11:74.

    PMID:
    20132550
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    12.

    A genome-wide survey of copy number variations in Han Chinese residing in Taiwan.

    Lin CH, Lin YC, Wu JY, Pan WH, Chen YT, Fann CS.

    Genomics. 2009 Oct;94(4):241-6. Epub 2009 Jun 25.

    PMID:
    19559783
    [PubMed - indexed for MEDLINE]
    13.

    Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies.

    Lee AS, Gutiérrez-Arcelus M, Perry GH, Vallender EJ, Johnson WE, Miller GM, Korbel JO, Lee C.

    Hum Mol Genet. 2008 Apr 15;17(8):1127-36. Epub 2008 Jan 7.

    PMID:
    18180252
    [PubMed - indexed for MEDLINE]
    Free Article
    14.

    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]
    Free PMC Article
    15.

    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]
    Free PMC Article
    16.

    Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis.

    Qiao Y, Liu X, Harvard C, Nolin SL, Brown WT, Koochek M, Holden JJ, Lewis ME, Rajcan-Separovic E.

    BMC Genomics. 2007 Jun 12;8:167.

    PMID:
    17565693
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    17.

    Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.

    Bruno DL, Ganesamoorthy D, Schoumans J, Bankier A, Coman D, Delatycki M, Gardner RJ, Hunter M, James PA, Kannu P, McGillivray G, Pachter N, Peters H, Rieubland C, Savarirayan R, Scheffer IE, Sheffield L, Tan T, White SM, Yeung A, Bowman Z, Ngo C, Choy KW, Cacheux V, Wong L, Amor DJ, Slater HR.

    J Med Genet. 2009 Feb;46(2):123-31. Epub 2008 Nov 17.

    PMID:
    19015223
    [PubMed - indexed for MEDLINE]
    18.

    Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.

    Cho SC, Yim SH, Yoo HK, Kim MY, Jung GY, Shin GW, Kim BN, Hwang JW, Kang JJ, Kim TM, Chung YJ.

    Psychiatr Genet. 2009 Aug;19(4):177-85.

    PMID:
    19407672
    [PubMed - indexed for MEDLINE]
    19.

    Application of Nexus copy number software for CNV detection and analysis.

    Darvishi K.

    Curr Protoc Hum Genet. 2010 Apr;Chapter 4:Unit 4.14.1-28.

    PMID:
    20373515
    [PubMed - indexed for MEDLINE]
    20.

    CGHScan: finding variable regions using high-density microarray comparative genomic hybridization data.

    Anderson BD, Gilson MC, Scott AA, Biehl BS, Glasner JD, Rajashekara G, Splitter GA, Perna NT.

    BMC Genomics. 2006 Apr 25;7:91.

    PMID:
    16638145
    [PubMed - indexed for MEDLINE]
    Free PMC Article

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