1Scrachan T, Abitbol M, Davidson D, et al. A new dimension for the human genome project: towards comprehensive expression maps [J]. Nat Genet, 1997, 16: 126-131.
2刘世新,刘艳.现代生物组织学技术[M].北京:科学出版社,2004.85-120.
3Drobyshev A, Mologina N, Shik V, et al. Sequence analysis by hybridization with oligonucleotide Microchip: identification of β-thalassemia mutations [J]. Gene, 1997, 188:4552 - 4555.
4Golub TR, Slonim DK, Tamayo P, et al. Molecular classification of cancer: class discovery and class prediction by gene expression monitoring [ J ]. Science, 1999, 286(5439): 531 -537.
5Hacia JG, Brody LC, Chee MS, et al. Detection of heterozygous mutation in BRCA1 using high density oligonucleotide arrays and two color fluorescence analysis [ J ]. Nat Genet,1996, 14 (4): 441-447.
6Chambers J, Angulo A, Amaratunga D, et al. DNA microarrays of the complex human cytomegalovirus genome:profiling kinetic class with drug sensitivity of viral gene expression [J]. J Virol, 1999, 73 (7): 5757-5766.
7Jellis CL. Defining critical residues in the epitope for HIV-neutralizing monoclonal antibody using phage ohsplay and peptide ar ray techmologies [ J]. Gene, 1993, 137: 63-68.
8Wilson M, Rerisi J, Kristensen HH, et al. Exploring druginduced alternation in gene expression in my cobaeterium tuberculosis by microarray hybridization [ J ]. Pro Nat1 Acids Sci (USA), 1999, 96 (22): 12833-12838.
10Laren M, Sobrine B, Phillips C, et al. Typing Y-chromosome single nucleotide poly morphisms with DNA microarray technology [ J ]. International Congress Series, 2003,1239:21-25.
二级参考文献29
1陶恩祥，中华神经科杂志，1998年，31卷，31页
2Chan P，Mov Disord，1997年，12卷，Suppl1期，26页
3Zhe Yu，Environ Mol Mutagen，2000年，36卷，201页
4马立人，生物芯片技术，2000年，6页
5Duggan D J，Nat Genet，1999年，21卷，supplement期，10页
6Amundson S A，Oncogene，1999年，18卷，24期，3666页
7Wang D G，Science，1998年，280卷，1077页
8Hacia J G，Nat Genet，1996年，14卷，4期，441页
9Schena M, Shalon D, Dais RW,et al. Quantitative monitoring of gene expression pattern with a complementary DNA microarray[J]. Science, 1995, 270(5235):467-470.
10Schena M, Shalon D, Heller R, et al. Parallel human genome analysis: Microarray-based expression monitoring of 1000 genes [J], PNAS USA, 1996,93:10614-10619.
2Amorim A, Pereira L. Pros and cons in the use of SNPs in forensic kinship investigation: a comparative analysis with STRs[J]. Forensic Sci Int, 2005, 150(1) : 17-21.
3Bφrsting C, Sanchez J J, Birk A H, et al. Comparison of paternity indices based on typing of 15 STRs, 7 VNTRs and 52 SNPs in 50 Danish mother-child-father trios [ J ]. International Congress Series, 2006, 1288: 436-438.
4Gill P. An assessment of the utility of single nucleotide polymorphisms (SNPs) for forensic purposes [ J ]. Int J Legal Med, 2001, 114(4-5) : 20,4-210.
5Bell P A, Chaturvedi S, Gelfand C A, et al. SNPstream UHT: uhra-high throughput SNP genotyping for pharmacogenomics and drug discovery [J]. Biotechniques, 2002, 74 (70-2) :76-77.
6Ahmadian A, Ehn M, Hober S. Pyrosequencing: History, biochemistry and future [ J ]. Clinica Chimica Acta, 2006, 363 : 83-94.
7Hardenbol P, Yu F, Belmont J, et al. Highly multiplexed molecular inversion probe genotyping: over 10 000 targeted SNPs genotyped in a single tube assay [ J ]. Genome Res, 2005, 15(2) : 269-275.
8Olson M V. Human genetics : Dr Watson's base pairs [ J ]. Nature, 2008, d52(7159) : 819-820.
9Nishida N, Koike A, Tajima A, et al. Evaluating the performance of Affymetrix SNP Array 6.0 platform with 400 Japanese individuals [ J ]. BMC Genomics, 2008, 22 ( 9 ) : 431.
10Pastinen T, Kurg A, Metspalu A, et al. Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays[ J]. Genome Res, 1997, 7(6): 606-614.
