Toward genome-wide SNP genotyping

被引:295
作者
Syvänen, AC [1 ]
机构
[1] Uppsala Univ, Dept Med Sci Mol Med, Univ Hosp, S-75185 Uppsala, Sweden
关键词
D O I
10.1038/ng1558
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genome-wide association studies with SNP markers are expected to allow identification of genes that underlie complex disorders. Hundreds of thousands of SNP markers will be required for comprehensive genome-wide association studies. The development of microarray-based methods for SNP genotyping on this scale remains a demanding task, despite many recent advances in technology for the production of high-density microarrays. A key technical obstacle is the PCR amplification step, which is required to reduce the complexity of and gain sufficient sensitivity for genotyping SNPs in large, diploid genomes. The multiplexing level that can be achieved in PCR does not match that of current microarray-based methods, making PCR the limiting step in the assays. Highly multiplexed microarray systems for SNP genotyping have recently been developed by combining well-known reaction principles for DNA amplification and SNP genotyping in clever ways. These new methods offer the potential of genome-wide SNP mapping of genes involved in complex diseases in the foreseeable future, provided that issues related to selection of the optimal SNP markers, sample throughput and the cost of the assays can be addressed.
引用
收藏
页码:S5 / S10
页数:6
相关论文
共 69 条
  • [1] An SNP map of the human genome generated by reduced representation shotgun sequencing
    Altshuler, D
    Pollara, VJ
    Cowles, CR
    Van Etten, WJ
    Baldwin, J
    Linton, L
    Lander, ES
    [J]. NATURE, 2000, 407 (6803) : 513 - 516
  • [2] [Anonymous], BIOTECHNIQUES S
  • [3] Parallel gene analysis with allele-specific padlock probes and tag microarrays -: art. no. e103
    Banér, J
    Isaksson, A
    Waldenström, E
    Jarvius, J
    Landegren, U
    Nilsson, M
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (17) : e103
  • [4] Bell PA, 2002, BIOTECHNIQUES, P70
  • [5] The elimination of primer-dimer accumulation in PCR
    Brownie, J
    Shawcross, S
    Theaker, J
    Whitcombe, D
    Ferrie, R
    Newton, C
    Little, S
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (16) : 3235 - 3241
  • [6] Flow cytometry-based minisequencing: A new platform for high-throughput single-nucleotide polymorphism scoring
    Cai, H
    White, PS
    Torney, D
    Deshpande, A
    Wang, ZL
    Marrone, B
    Nolan, JP
    [J]. GENOMICS, 2000, 66 (02) : 135 - 143
  • [7] A microsphere-based assay for multiplexed single nucleotide polymorphism analysis using single base chain extension
    Chen, JW
    Iannone, MA
    Li, MS
    Taylor, JD
    Rivers, P
    Nelsen, AJ
    Slentz-Kesler, KA
    Roses, A
    Weiner, MP
    [J]. GENOME RESEARCH, 2000, 10 (04) : 549 - 557
  • [8] Template-directed dye-terminator incorporation (TDI) assay: A homogeneous DNA diagnostic method based on fluorescence resonance energy transfer
    Chen, XN
    Kwok, PY
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (02) : 347 - 353
  • [9] Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations
    Crawford, DC
    Carlson, CS
    Rieder, MJ
    Carrington, DP
    Yi, Q
    Smith, JD
    Eberle, MA
    Kruglyak, L
    Nickerson, DA
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (04) : 610 - 622
  • [10] High-throughput variation detection and genotyping using microarrays
    Cutler, DJ
    Zwick, ME
    Carrasquillo, MM
    Yohn, CT
    Tobin, KP
    Kashuk, C
    Mathews, DJ
    Shah, NA
    Eichler, EE
    Warrington, JA
    Chakravarti, A
    [J]. GENOME RESEARCH, 2001, 11 (11) : 1913 - 1925