메뉴 건너뛰기




Volumn 4, Issue 4, 1999, Pages 339-343

High throughput fluorescent CE-SSCP SNP genotyping

Author keywords

Capillary electrophoresis; Genotyping; Polymorphism; SNP

Indexed keywords

FLUORESCENT DYE; NUCLEOTIDE; SINGLE STRANDED DNA;

EID: 0032871581     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.mp.4000564     Document Type: Article
Times cited : (23)

References (28)
  • 1
    • 0031697439 scopus 로고    scopus 로고
    • Reading bits of genetic information: Methods for single-nucleotide polymorphism analysis
    • Landegren U, Nilsson M, Kwok P. Reading bits of genetic information: methods for single-nucleotide polymorphism analysis. Genome Res 1998; 8: 769-776.
    • (1998) Genome Res , vol.8 , pp. 769-776
    • Landegren, U.1    Nilsson, M.2    Kwok, P.3
  • 3
    • 0032524383 scopus 로고    scopus 로고
    • Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
    • Wang D, Fan J, Siao C, Berno A, Young P, Sapolsky R et al. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. Science 1998; 280: 1077-1082.
    • (1998) Science , vol.280 , pp. 1077-1082
    • Wang, D.1    Fan, J.2    Siao, C.3    Berno, A.4    Young, P.5    Sapolsky, R.6
  • 5
    • 0033018816 scopus 로고    scopus 로고
    • Reliable identification of large numbers of candidate SNPs from public EST data
    • Buetow K, Edmonson M, Cassidy A, Reliable identification of large numbers of candidate SNPs from public EST data. Nature Genet 1999; 21: 323-325.
    • (1999) Nature Genet , vol.21 , pp. 323-325
    • Buetow, K.1    Edmonson, M.2    Cassidy, A.3
  • 6
    • 4243830825 scopus 로고    scopus 로고
    • A new automated high-throughput multiple capillary electrophoresis platform for microsatellite analysis
    • Munnely KD, Caffo N, Tynan K, Hennessey K, Wike CM. A new automated high-throughput multiple capillary electrophoresis platform for microsatellite analysis. Am J Hum Genet 1998; 63: A238.
    • (1998) Am J Hum Genet , vol.63
    • Munnely, K.D.1    Caffo, N.2    Tynan, K.3    Hennessey, K.4    Wike, C.M.5
  • 7
    • 0030895285 scopus 로고    scopus 로고
    • Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder
    • Karayiorgou M, Alternus M, Galke B, Goldman D, Murphy D, Ott J. et al. Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder. Proc Natl Acad Sci USA 1997; 94: 4572-1575.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 4572-1575
    • Karayiorgou, M.1    Alternus, M.2    Galke, B.3    Goldman, D.4    Murphy, D.5    Ott, J.6
  • 8
    • 0031557407 scopus 로고    scopus 로고
    • Human 5-HT5A receptor gene: Systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5′ untranslated region
    • Shimron-Abarbanell D, Erdmann J, Vogt I, Bryant S, Spurr N, Knapp M et al. Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5′ untranslated region. Biochem Biophys Res Commun 1997; 233: 6-9.
    • (1997) Biochem Biophys Res Commun , vol.233 , pp. 6-9
    • Shimron-Abarbanell, D.1    Erdmann, J.2    Vogt, I.3    Bryant, S.4    Spurr, N.5    Knapp, M.6
  • 9
    • 0027300190 scopus 로고
    • An Mspl polymorphism in the human serotonin receptor gene (HTR2): Detection by DGGE and RFLP analysis
    • Warren J, Peacock M, Rodriguez L, Fink J. An Mspl polymorphism in the human serotonin receptor gene (HTR2): detection by DGGE and RFLP analysis. Hum Mol Genet 1993; 2: 338.
    • (1993) Hum Mol Genet , vol.2 , pp. 338
    • Warren, J.1    Peacock, M.2    Rodriguez, L.3    Fink, J.4
  • 10
    • 0031561157 scopus 로고    scopus 로고
    • Association between 5-HT2A gene promoter polymorphism and anorexia nervosa
    • Collier D, Arranz M, Li T, Mupita D, Brown N, Treasure J. Association between 5-HT2A gene promoter polymorphism and anorexia nervosa. Lancet 1997; 350: 412.
    • (1997) Lancet , vol.350 , pp. 412
    • Collier, D.1    Arranz, M.2    Li, T.3    Mupita, D.4    Brown, N.5    Treasure, J.6
  • 11
    • 0028904290 scopus 로고
    • Mapping of the serotonin 5HT1D alpha autoreceptor gene (HTR1D) on chromosome 1 using a silent polymorphism in the coding region
    • Ozaki N, Lappalainen J, Dean M, Virkkunen M, Linnoila M, Goldman D. Mapping of the serotonin 5HT1D alpha autoreceptor gene (HTR1D) on chromosome 1 using a silent polymorphism in the coding region. Am J Med Genet 1995; 60: 162-164.
    • (1995) Am J Med Genet , vol.60 , pp. 162-164
    • Ozaki, N.1    Lappalainen, J.2    Dean, M.3    Virkkunen, M.4    Linnoila, M.5    Goldman, D.6
  • 12
    • 0024046092 scopus 로고
    • Human monoamine oxidase gene (MAOA): Chromosome position (Xp21-p11) and DNA polymorphism
    • Ozelius L, Hsu Y, Bruns G, Powell J, Chen S, Weyler W et al. Human monoamine oxidase gene (MAOA): chromosome position (Xp21-p11) and DNA polymorphism. Genomics 1988; 3: 53-58.
    • (1988) Genomics , vol.3 , pp. 53-58
    • Ozelius, L.1    Hsu, Y.2    Bruns, G.3    Powell, J.4    Chen, S.5    Weyler, W.6
  • 13
    • 0029032864 scopus 로고
    • Identification, expression, and pharmacology of a Cys23-Ser23 substitution in the human 5-HT2C receptor gene (HTR2C)
    • Lappalainen J, Zhang L, Dean M, Oz M, Ozaki N, Yu D et al. Identification, expression, and pharmacology of a Cys23-Ser23 substitution in the human 5-HT2C receptor gene (HTR2C). Genomics 1995; 27: 274-279.
    • (1995) Genomics , vol.27 , pp. 274-279
    • Lappalainen, J.1    Zhang, L.2    Dean, M.3    Oz, M.4    Ozaki, N.5    Yu, D.6
  • 15
    • 0031731325 scopus 로고    scopus 로고
    • Microsatellite marker content mapping of 12 candidate genes for obesity: Assembly of seven obesity screening panels for automated genotyping
    • Winick J Friedman J. Microsatellite marker content mapping of 12 candidate genes for obesity: assembly of seven obesity screening panels for automated genotyping. Genome Res 1998; 8: 985-994.
    • (1998) Genome Res , vol.8 , pp. 985-994
    • Winick, J.1    Friedman, J.2
  • 16
    • 0032231888 scopus 로고    scopus 로고
    • Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase
    • Clark AG, Weiss KM, Nickerson DA, Taylor SL, Buchanan A, Stengard J et al. Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase. Am J Hum Genet 1998; 63: 595-612.
    • (1998) Am J Hum Genet , vol.63 , pp. 595-612
    • Clark, A.G.1    Weiss, K.M.2    Nickerson, D.A.3    Taylor, S.L.4    Buchanan, A.5    Stengard, J.6
  • 17
    • 0031263204 scopus 로고    scopus 로고
    • A streamlined mutation detection system: Multicolor post-PCR fluorescence labeling and single-strand conformational polymorphism analysis by capillary electrophoresis
    • Inazuka M, Wenz H, Sakabe M, Tahira T, Hayashi K. A streamlined mutation detection system: multicolor post-PCR fluorescence labeling and single-strand conformational polymorphism analysis by capillary electrophoresis. Genome Res 1997; 7: 1094-1103.
    • (1997) Genome Res , vol.7 , pp. 1094-1103
    • Inazuka, M.1    Wenz, H.2    Sakabe, M.3    Tahira, T.4    Hayashi, K.5
  • 18
    • 0033016069 scopus 로고    scopus 로고
    • Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography
    • Hoogendoorn B, Owen M, Oefner P, Williams N, Austin J, O'Donnovan M. Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography. Hum Genet 1999; 104: 89-93.
    • (1999) Hum Genet , vol.104 , pp. 89-93
    • Hoogendoorn, B.1    Owen, M.2    Oefner, P.3    Williams, N.4    Austin, J.5    O'Donnovan, M.6
  • 19
    • 84984934752 scopus 로고    scopus 로고
    • Resequencing and mutational analysis using oligonucleotide microarrays
    • Hacia J. Resequencing and mutational analysis using oligonucleotide microarrays. Nature Genet Suppl 1999; 21: 42-47.
    • (1999) Nature Genet Suppl , vol.21 , pp. 42-47
    • Hacia, J.1
  • 20
    • 0031737198 scopus 로고    scopus 로고
    • Applications of DNA chips for genomic analysis
    • Hacia J, Brody L, Collins F. Applications of DNA chips for genomic analysis. Mol Psychiatry 1998; 3: 483-492.
    • (1998) Mol Psychiatry , vol.3 , pp. 483-492
    • Hacia, J.1    Brody, L.2    Collins, F.3
  • 21
    • 0033041685 scopus 로고    scopus 로고
    • High-throughput polymorphism screening and genotyping with high-density oligonucleotide arrays
    • Sapolsky R, Hsie L, Berno A, Ghandour G, Mittmann M, Fan J. High-throughput polymorphism screening and genotyping with high-density oligonucleotide arrays. Genet Anal 1999; 14: 187-192.
    • (1999) Genet Anal , vol.14 , pp. 187-192
    • Sapolsky, R.1    Hsie, L.2    Berno, A.3    Ghandour, G.4    Mittmann, M.5    Fan, J.6
  • 22
    • 0033005014 scopus 로고    scopus 로고
    • Fluorescent allele-specific PCR (FAS-PCR) improves the reliability of single nucleotide polymorphism screening
    • Howard T, Bleecker E, Stine O. Fluorescent allele-specific PCR (FAS-PCR) improves the reliability of single nucleotide polymorphism screening. Biotechniques 1999; 26: 380-381.
    • (1999) Biotechniques , vol.26 , pp. 380-381
    • Howard, T.1    Bleecker, E.2    Stine, O.3
  • 23
    • 0030885877 scopus 로고    scopus 로고
    • Fluorescence energy transfer detection as a homozygous DNA diagnostic method
    • Chen X, Zehnbauer B, Gnirke A, Kwok P. Fluorescence energy transfer detection as a homozygous DNA diagnostic method. Proc Natl Acad Sci 1997; 94: 10756-10761.
    • (1997) Proc Natl Acad Sci , vol.94 , pp. 10756-10761
    • Chen, X.1    Zehnbauer, B.2    Gnirke, A.3    Kwok, P.4
  • 24
    • 0031679495 scopus 로고    scopus 로고
    • Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population
    • Pastinen T, Perola M, Niini P, Terwilliger J, Salomaa V, Vartiainen E et al. Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population. Hum Mol Genet 1998; 7: 1453-1462.
    • (1998) Hum Mol Genet , vol.7 , pp. 1453-1462
    • Pastinen, T.1    Perola, M.2    Niini, P.3    Terwilliger, J.4    Salomaa, V.5    Vartiainen, E.6
  • 25
    • 0032973093 scopus 로고    scopus 로고
    • A rapid automated SSCP multiplex capillary electrophoresis protocol that detects the two common mutations implicated in hereditary hemochromatosis (HH)
    • Wenz H, Baumheuter S, Ramachandra S, Worwood M. A rapid automated SSCP multiplex capillary electrophoresis protocol that detects the two common mutations implicated in hereditary hemochromatosis (HH). Hum Genet 1999; 104: 29-35.
    • (1999) Hum Genet , vol.104 , pp. 29-35
    • Wenz, H.1    Baumheuter, S.2    Ramachandra, S.3    Worwood, M.4
  • 26
    • 0032968854 scopus 로고    scopus 로고
    • Recent enhancements in SSCP
    • Hayashi K. Recent enhancements in SSCP. Genet Anal 1999; 14: 193-196.
    • (1999) Genet Anal , vol.14 , pp. 193-196
    • Hayashi, K.1
  • 27
    • 0033059484 scopus 로고    scopus 로고
    • Detection of polymorphism in the RING3 gene by high throughput fluorescent SSCP analysis
    • Thorpe K, Schafer A, Cénin E, Trowsdale J, Beck S. Detection of polymorphism in the RING3 gene by high throughput fluorescent SSCP analysis. Immunogenetics 1999; 49: 256-265.
    • (1999) Immunogenetics , vol.49 , pp. 256-265
    • Thorpe, K.1    Schafer, A.2    Cénin, E.3    Trowsdale, J.4    Beck, S.5
  • 28
    • 0031669184 scopus 로고    scopus 로고
    • Overlapping genomic sequences: A treasure trove of single nucleotide polymorphisms
    • Taillon-Miller P, Gu Z, Li Q, Hiller L, Kwok P. Overlapping genomic sequences: a treasure trove of single nucleotide polymorphisms. Genome Res 1998; 8: 748-754.
    • (1998) Genome Res , vol.8 , pp. 748-754
    • Taillon-Miller, P.1    Gu, Z.2    Li, Q.3    Hiller, L.4    Kwok, P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.