High-resolution analysis of chromosomal imbalances using the Affymetrix 10K SNP genotyping chip

被引:21
作者
Herr, A
Grützmann, R
Matthaei, A
Artelt, J
Schröck, E
Rump, A
Pilarsky, C
机构
[1] Med Fac Carl Gustav Carus, Inst Clin Genet, D-01307 Dresden, Germany
[2] Dresden Univ Technol, Hosp Carl Gustav Carus, Dept Visceral Thorac & Vasc Surg, D-01307 Dresden, Germany
关键词
SNP; array CGH; genome-wide; oligonucleotide microarray; LOH;
D O I
10.1016/j.ygeno.2004.07.015
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Array-based comparative genome hybridization is a powerful tool for detecting chromosomal imbalances at high resolution, However, the design and setup of such arrays are time consuming and expensive and thus worthwhile only when large numbers of arrays will be processed. To provide a feasible solution, we have developed an algorithm that renders the publicly available Affymetrix I OK SNP genotyping chip useful for high-resolution analysis of chromosomal imbalances. We have used our newly developed algorithm to analyze data from Affymetrix 10K chips that were hybridized with DNA probes from a variety of different sources, such as primary tumors, cell lines, and blood from patients with unbalanced translocations. In summary, we were able to (i) demonstrate the capability of our method by reproduction of published and unpublished data obtained with alternative methods and (ii) identify novel imbalances that were not shown before. (c) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:392 / 400
页数:9
相关论文
共 24 条
  • [1] Genomic microarrays in human genetic disease and cancer
    Albertson, DG
    Pinkel, D
    [J]. HUMAN MOLECULAR GENETICS, 2003, 12 : R145 - R152
  • [2] Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene
    Albertson, DG
    Ylstra, B
    Segraves, R
    Collins, C
    Dairkee, SH
    Kowbel, D
    Kuo, WL
    Gray, JW
    Pinkel, D
    [J]. NATURE GENETICS, 2000, 25 (02) : 144 - 146
  • [3] A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region
    Bartsch, O
    Hinkel, GK
    Petersen, MB
    Konig, U
    Bugge, M
    Mikkelsen, M
    Avramopoulos, D
    Morris, M
    Antonarakis, SE
    [J]. HUMAN GENETICS, 1997, 100 (5-6) : 669 - 675
  • [4] THE EVOLUTIONARILY CONSERVED KRUPPEL-ASSOCIATED BOX DOMAIN DEFINES A SUBFAMILY OF EUKARYOTIC MULTIFINGERED PROTEINS
    BELLEFROID, EJ
    PONCELET, DA
    LECOCQ, PJ
    REVELANT, O
    MARTIAL, JA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) : 3608 - 3612
  • [5] High-resolution analysis of DNA copy number using oligonucleotide microarrays
    Bignell, GR
    Huang, J
    Greshock, J
    Watt, S
    Butler, A
    West, S
    Grigorova, M
    Jones, KW
    Wei, W
    Stratton, MR
    Futreal, PA
    Weber, B
    Shapero, MH
    Wooster, R
    [J]. GENOME RESEARCH, 2004, 14 (02) : 287 - 295
  • [6] Genomic instability and cancer
    Charames, GS
    Bapat, B
    [J]. CURRENT MOLECULAR MEDICINE, 2003, 3 (07) : 589 - 596
  • [7] IN-VITRO CULTIVATION OF HUMAN TUMORS - ESTABLISHMENT OF CELL LINES DERIVED FROM A SERIES OF SOLID TUMORS
    GIARD, DJ
    AARONSON, SA
    TODARO, GJ
    ARNSTEIN, P
    KERSEY, JH
    DOSIK, H
    PARKS, WP
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1973, 51 (05) : 1417 - 1423
  • [8] Heng Henry HQ, 2004, Cell Chromosome, V3, P1, DOI 10.1186/1475-9268-3-1
  • [9] Hyman E, 2002, CANCER RES, V62, P6240
  • [10] A tiling resolution DNA microarray with complete coverage of the human genome
    Ishkanian, AS
    Malloff, CA
    Watson, SK
    deLeeuw, RJ
    Chi, B
    Coe, BP
    Snijders, A
    Albertson, DG
    Pinkel, D
    Marra, MA
    Ling, V
    MacAulay, C
    Lam, WL
    [J]. NATURE GENETICS, 2004, 36 (03) : 299 - 303