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Single-nucleotide polymorphism array

Primdahl H, Wikman FP, von der Maase H et al. Allelic imbalances in human bladder cancer genome-wide detection with high-density single-nucleotide polymorphism arrays. J Natl Cancer Inst 2002 94 216-223. [Pg.15]

Use of Single-Nucleotide Polymorphism Array for Tumor Aberrations in Gene Copy Numbers... [Pg.75]

Key Words single nucleotide polymorphism array allelic imbalance copy nmn-ber variation whole-genome amplification formalin-fixed and parafiin-embedded tissue... [Pg.76]

Janne PA, Li C, Zhao X et al. High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines. Oncogene 2004 23 2716-2726. [Pg.86]

Hoque MO, Lee J, Begum S et al. High-throughput molecular analysis of urine sediment for the detection of bladder eaneer by high-density single-nucleotide polymorphism array. Cancer Res 2003 63 5723-5726. [Pg.87]

Lindblad-Toh K, Tanenbaum DM, Daly MJ et al. Loss-of-heterozygosity analysis of small-eell lung carcinomas using single-nucleotide polymorphism arrays. Nat Biotechnol 2000 18 1001-1005. [Pg.87]

Zhao X, Li C, Paez JG et al. An integrated view of eopy number and allelic alterations in the eaneer genome using single nucleotide polymorphism arrays. Cancer Res 2004 64 3060-3071. [Pg.87]

Lips EH, Dierssen JW, van Eijk R et al. Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single-nucleotide polymorphism arrays. Cancer 2005 65 10188-10191. [Pg.88]

Stark, M. and Hayward, N. (2007). Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays. Cancer Res. 67, 2632-2642. [Pg.308]

Armstrong, B. et al. (2000) Suspension arrays for high throughput, multiplexed single nucleotide polymorphism genotyping. Cytometry 40, 102-108. [Pg.1044]

Wong KK, Tsang YT, Shen J et al. Allelic imbalance analysis by high-density single-nucleotide polymorphic allele (SNP) array with whole genome amplified DNA. Nucleic Acids Res 2004 32 e69. [Pg.86]

Nannya Y, Sanada M, Nakazaki K et al. A robust algorithm for copy number detection using high-density oligonucleotide single-nucleotide polymorphism genotyping arrays. Cancer Res 2005 65 6071-6079. [Pg.86]

Lieberfarb ME, Lin M, Lechpammer M et al. Genome-wide loss of heterozygosity analysis from laser capture microdissected prostate eaneer using single nucleotide polymorphic allele (SNP) arrays and a novel bioinformaties platform dChipSNP. Cancer Res 2003 63 4781 785. [Pg.87]

Wong KK, Tsang YT, Chang YM et al. Genome-wide allelie imbalanee analysis of pediatric gliomas by single nucleotide polymorphic allele array. Cancer Res 2006 66 11172-11178. [Pg.87]

Holloway, J. W. Beghe, B. Turner, S. Hinks, L. J. Day, I. N. Howell, W. M. Comparison of three methods for single nucleotide polymorphism typing for DNA bank studies sequence-specific oligonucleotide probe hybridisation, TaqMan liquid phase hybridisation, and microplate array diagonal gel electrophoresis (MADGE). Hum. Mutat. 1999,14(4), 340-347. [Pg.431]

Medintz, I., Wong, W.W., Sensabaugh, G., Mathies, R.A., High speed single nucleotide polymorphism typing of a hereditary haemochromatosis mutation with capillary array electrophoresis microplates. Electrophoresis 2000, 21, 2352-2358. [Pg.463]

Since microarrays are simply spots of DNA arrayed in a known pattern, they also can be used for DNA-DNA hybridization studies. This is the basis for using micro-arrays for comparative DNA hybridizations, single nucleotide polymorphism (SNP) discovery, and chromatin immunoprecipiation followed by microarray chip hybridization (ChIP on chip analyses) to identify transcription factor binding sites (discussed below). [Pg.32]


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