1. Wang DG, Fan J-B, Siao C-J, et al. (1998) Large-scale identification, mapping and genotyping of single-nucleotide polymorphisms in the human genome. Science 280: 1077-1082.

2. Li WH and Sadler LA (1991) Low nucleotide diversity in man. Genetics 129: 513-523.

3. Sachidanandam R, Weissman D, Schmidt SC, et al. (2001) A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 409: 928-933.

4. Cooper DN, Ball EV, and Krawczak M (1998) The human gene mutation database. Nucleic Acids Res. 26: 285-287.

5. Ng PC and Henikoff S (2002) Accounting for human polymorphisms predicted to affect protein function. Genome Res 12: 436-446.

6. Collins FS, Brooks LD and Chakravarti AA (1998) DNA polymorphism discovery resource for research on human genetic variation. Genome Res 8: 1229-1231.

7. Schafer AL and Hawkins JR (1998) DNA variation and the future of human genetics. Nature Biotech. 16: 33-39.

8. Jin P and Wang E (2003) Polymorphism in clinical immunology. From HLA typing to immunogenetic profiling. J Transl Med 1: 8.

9. Howell WM, Calder PC and Grimble RF (2002) Gene polymorphisms, inflammatory diseases and cancer. Proc Nutr Soc 61: 447-456.

10. Haukim N, Bidwell JL, Smith AJP, et al. (2002) Cytokine gene polymorphism in human disease: on-line databases, supplement 2. Genes Immunol 3: 313-330.

11. van Sorge NM, van der Pol W-L and van de Winkel JGJ (2003) FCgR polymorphisms: implications for function, disease susceptibility and immunotherapy. 61: 202.

12. Parham P (2003) Immunogenetics of killer-cell immunoglobulin-like receptors. Tissue Antigens 62: 194-200.

13. Kwok P-Y (2001) Genetic association by whole-genome analysis. Science 294: 2669-2670.

14. Adams SD, Barracchini KC, Chen D, Robbins F, Wang L, Larsen P, Luhm R and Stroncek DF (2004) Ambiguous allele combinations in HLA Class I and Class II sequence-based typing: when precise nucleotide sequencing leads to imprecise allele identification. J Transl Med 2: 30.

15. Wasson J, Skolnick G, Love-Gregory L and Permutt MA (2002) Assessing allele frequencies of single nucleotide polymorphisms in DNA pools by pyrose-quencing technology. Biotechniques 32: 1144-6, 1148, 1150.

16. Gruber JD, Colligan PB and Wolford JK (2002) Estimation of single nucleotide polymorphism allele frequency in DNA pools by using Pyrosequencing. Hum Genet 110: 395-401.

17. Sauer S and Gut IG (2002) Genotyping single-nucleotide polymorphisms by matrix-assisted laser-desorption/ionization time-of-flight mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci 782: 73-87.

18. Krebs S, Medugorac I, Seichter D and Forster M (2003) RNaseCut: a MALDI mass spectrometry-based method for SNP discovery. Nucleic Acids Res 31: e37.

19. Kim S, Shi S, Bonome T, Ulz ME, Edwards JR, Fodstad H, Russo JJ and Ju J (2003) Multiplex genotyping of the human beta2-adrenergic receptor gene using solidphase capturable dideoxynucleotides and mass spectrometry. Anal Biochem 316: 251-258.

20. Hacia JG, Brody LC, Chee MS, Fodor SP and Collins FS (1996) Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis [see comments]. Nat Genet 14: 441-447.

21. Kwok PY (2001) Methods for genotyping single nucleotide polymorphisms. Annu Rev Genomics Hum Genet 2: 235-258.

22. Turner D, Choudhury F, Reynard M, Railton D and Navarrete C (2002) Typing of multiple single nucleotide polymorphisms in cytokine and receptor genes using SNaPshot. Hum Immunol 63: 508-513.

23. Guo Z, Gatterman MS, Hood L, Hansen JA and Petersdorf EW (2002) Oligonucleotide arrays for high-throughput SNPs detection in the MHC class I genes: HLA-B as a model system. Genome Res 12: 447-457.

24. Chee M, Yang R, Hubbell E, et al. (1996) Accessing genetic information with high-density DNA arrays. Science 274: 610-614.

25. Hacia JG (1999) Resequencing and mutational analysis using oligonucleotide microarrays. Nat Genet 21: 42-47.

26. Hacia JG, Sun B, Hunt N, Edgemon K, Mosbrook D, Robbins C, Fodor SP, Tagle DA and Collins FS (1998) Strategies for mutational analysis of the large multiexon ATM gene using high-density oligonucleotide arrays. Genome Res 8: 1245-1258.

27. Patil N, Berno AJ, Hinds DA, et al. (2001) Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science 294: 1719-1723.

28. Lee I, Dombkowski AA and Athey BD (2004) Guidelines for incorporating non-perfectly matched oligonucleotides into target-specific hybridization probes for a DNA microarray. Nucleic Acids Res 32: 681-690.

29. Wang E, Adams S, Zhao Y, Panelli MC, Simon R, Klein H and Marincola FM (2003) A strategy for detection of known and unknown SNP using a minimum number of oligonucleotides. J Transl Med 1: 4.

30. Swets JA (1988) Measuring the accuracy of diagnostic systems. Science 240: 1285-1293.

31. International SNP Map Working Group (2001) A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 409: 928-933.

32. Keen LJ (2002) The extent and analysis of cytokine and cytokine receptor gene polymorphism. Transpl Immunol 10: 143-146.

33. McCarron SL, Edwards S, Evans PR, et al. (2002) Influence of cytokine gene polymorphism on the development of prostate cancer. Cancer Res 62: 33693372.

34. Howell WM, Turner SJ, Bateman AC, and Theaker JM (2001) IL-10 promoter polymorphisms influence tumour development in cutaneous malignant melanoma. Genes Immunol 2: 25-31.

35. Wang D, Coscoy L, Zylberberg M, Avila PC, Boushey HA, Ganem D and DeRisi JL (2002) Microarray-based detection and genotyping of viral pathogens. Proc Natl Acad Sci USA 99: 15687-15692.

36. Liu CL, Schreiber SL and Bernstein BE (2003) Development and validation of a T7 based linear amplification for genomic DNA. BMC Genomics 4: 19.

37. Klein CA, Schmidt-Kittler O, Schardt JA, Pantel K, Speicher MR and Riethmuller G (1999) Comparative genomic hybridization, loss of heterozygosity, and DNA sequence analysis of single cells. Proc Natl Acad Sci USA 96: 4494-4499.

38. Hosono S, Faruqi AF, Dean FB, et al. (2003) Unbiased whole-genome amplification directly from clinical samples. Genome Res 13: 954-964.

39. Paez JG, Lin M, Beroukhim R, et al. (2004) Genome coverage and sequence fidelity of phi29 polymerase-based multiple strand displacement whole genome amplification. Nucleic Acids Res 32: e71.

40. Telenius H, Carter NP, Bebb CE, Nordenskjold M, Ponder BA and Tunnacliffe A (1992) Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 13: 718-725.

41. Jordan B, Charest A, Dowd JF, Blumenstiel JP, Yeh RF, Osman A, Housman DE and Landers JE (2002) Genome complexity reduction for SNP genotyping analysis. Proc Natl Acad Sci USA 99: 2942-2947.

42. Kwok PY (2002) Making 'random amplification' predictable in whole genome analysis. Trends Biotechnol 20: 411-412.

43. Zhang L, Cui X, Schmitt K, Hubert R, Navidi W and Arnheim N (1992) Whole genome amplification from a single cell: implications for genetic analysis. Proc Natl Acad Sci USA 89: 5847-5851.

44. Pirker C, Raidl M, Steiner E, et al. (2004) Whole genome amplification for CGH analysis: Linker-adapter PCR as the method of choice for difficult and limited samples. Cytometry 61A: 26-34.

45. Barker DL, Hansen MS, Faruqi AF, et al. (2004) Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel. Genome Res 14: 901-907.

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