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Volumn 75, Issue 4, 2004, Pages 647-653

Sequence-based linkage analysis

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 19; COMPUTER SIMULATION; CONFIDENCE INTERVAL; CONTROLLED STUDY; DNA SEQUENCE; GENE NUMBER; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC MARKER; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; HUMAN GENOME; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SEQUENCE ANALYSIS; TECHNIQUE; VALIDATION PROCESS;

EID: 4544377156     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/424888     Document Type: Article
Times cited : (3)

References (32)
  • 1
    • 0036338150 scopus 로고    scopus 로고
    • Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees
    • Abecasis GR, Cherny SS, Cookson WO, Cardon LR (2002) Merlin - rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30:97-101
    • (2002) Nat Genet , vol.30 , pp. 97-101
    • Abecasis, G.R.1    Cherny, S.S.2    Cookson, W.O.3    Cardon, L.R.4
  • 2
    • 0036208832 scopus 로고    scopus 로고
    • Patterns of linkage disequilibrium in the human genome
    • Ardlie KG, Kruglyak L, Seielstad M (2002) Patterns of linkage disequilibrium in the human genome. Nat Rev Genet 3:299-309
    • (2002) Nat Rev Genet , vol.3 , pp. 299-309
    • Ardlie, K.G.1    Kruglyak, L.2    Seielstad, M.3
  • 4
    • 0019302053 scopus 로고
    • Construction of a genetic linkage map in man using restriction fragment length polymorphisms
    • Botstein D, White DL, Skolnick M, Davis RW (1980) Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am J Hum Genet 32:314-331
    • (1980) Am J Hum Genet , vol.32 , pp. 314-331
    • Botstein, D.1    White, D.L.2    Skolnick, M.3    Davis, R.W.4
  • 6
    • 0031978181 scopus 로고    scopus 로고
    • Base-calling of automated sequencer traces using Phred. II. Error probabilities
    • Ewing B, Green P (1998) Base-calling of automated sequencer traces using Phred. II. Error probabilities. Genome Res 8:186-194
    • (1998) Genome Res , vol.8 , pp. 186-194
    • Ewing, B.1    Green, P.2
  • 7
    • 0031955518 scopus 로고    scopus 로고
    • Base-calling of automated sequencer traces using Phred. I. Accuracy assessment
    • Ewing B, Hillier L, Wendl MC, Green P (1998) Base-calling of automated sequencer traces using Phred. I. Accuracy assessment. Genome Res 8:175-185
    • (1998) Genome Res , vol.8 , pp. 175-185
    • Ewing, B.1    Hillier, L.2    Wendl, M.C.3    Green, P.4
  • 8
    • 0036128504 scopus 로고    scopus 로고
    • Maps for cost-effective genome screens using diallelic markers
    • Goddard KA, Wijsman E (2002) Maps for cost-effective genome screens using diallelic markers. Genet Epidemiol 22:205-220
    • (2002) Genet Epidemiol , vol.22 , pp. 205-220
    • Goddard, K.A.1    Wijsman, E.2
  • 9
    • 0031955116 scopus 로고    scopus 로고
    • Consed: A graphical tool for sequence finishing
    • Gordon D, Abajian C, Green P (1998) Consed: a graphical tool for sequence finishing. Genome Res 8:195-202
    • (1998) Genome Res , vol.8 , pp. 195-202
    • Gordon, D.1    Abajian, C.2    Green, P.3
  • 11
    • 0036184745 scopus 로고    scopus 로고
    • Generating samples under a Wright-Fisher neutral model of genetic variation
    • Hudson RR (2002) Generating samples under a Wright-Fisher neutral model of genetic variation. Bioinformatics 18:337-338
    • (2002) Bioinformatics , vol.18 , pp. 337-338
    • Hudson, R.R.1
  • 15
    • 0346753823 scopus 로고    scopus 로고
    • Ultrafast DNA sequencing
    • Kling J (2003) Ultrafast DNA sequencing. Nat Biotechnol 21:1425-1427
    • (2003) Nat Biotechnol , vol.21 , pp. 1425-1427
    • Kling, J.1
  • 17
    • 0030861903 scopus 로고    scopus 로고
    • The use of a genetic map of biallelic markers in linkage studies
    • Kruglyak L (1997) The use of a genetic map of biallelic markers in linkage studies. Nat Genet 17:21-24
    • (1997) Nat Genet , vol.17 , pp. 21-24
    • Kruglyak, L.1
  • 18
    • 0029886532 scopus 로고    scopus 로고
    • Parametric and nonparametric linkage analysis: A unified multipoint approach
    • Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES (1996) Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 58:1347-1363
    • (1996) Am J Hum Genet , vol.58 , pp. 1347-1363
    • Kruglyak, L.1    Daly, M.J.2    Reeve-Daly, M.P.3    Lander, E.S.4
  • 19
    • 0029805706 scopus 로고    scopus 로고
    • The new genomics: Global views of biology
    • Lander ES (1996) The new genomics: global views of biology. Science 274:536-539
    • (1996) Science , vol.274 , pp. 536-539
    • Lander, E.S.1
  • 20
    • 0035071608 scopus 로고    scopus 로고
    • Efficient multipoint linkage analysis through reduction of inheritance space
    • Markianos K, Daly MJ, Kruglyak L (2001) Efficient multipoint linkage analysis through reduction of inheritance space. Am J Hum Genet 68:963-977
    • (2001) Am J Hum Genet , vol.68 , pp. 963-977
    • Markianos, K.1    Daly, M.J.2    Kruglyak, L.3
  • 24
    • 0030872838 scopus 로고    scopus 로고
    • PolyPhred: Automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing
    • Nickerson DA, Tobe VO, Taylor SL (1997) PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing. Nucleic Acids Res 25:2745-2751
    • (1997) Nucleic Acids Res , vol.25 , pp. 2745-2751
    • Nickerson, D.A.1    Tobe, V.O.2    Taylor, S.L.3
  • 25
    • 0036275126 scopus 로고    scopus 로고
    • BeadArray™ technology: Enabling an accurate, cost-effective approach to high-throughput genotyping
    • Oliphant A, Barker D, Stuelpnagel JR, Chee MS (2002) BeadArray™ technology: enabling an accurate, cost-effective approach to high-throughput genotyping. Biotechniques Suppl 32:56-61
    • (2002) Biotechniques Suppl , vol.32 , pp. 56-61
    • Oliphant, A.1    Barker, D.2    Stuelpnagel, J.R.3    Chee, M.S.4
  • 26
    • 0034977045 scopus 로고    scopus 로고
    • Linkage disequilibrium in humans: Models and data
    • Pritchard JK, Przeworski M (2001) Linkage disequilibrium in humans: models and data. Am J Hum Genet 69:1-14
    • (2001) Am J Hum Genet , vol.69 , pp. 1-14
    • Pritchard, J.K.1    Przeworski, M.2
  • 27
    • 0032906340 scopus 로고    scopus 로고
    • Sequence variation in the human angiotensin converting enzyme
    • Rieder MJ, Taylor SL, Clark AG, Nickerson DA (1999) Sequence variation in the human angiotensin converting enzyme. Nat Genet 22:59-62
    • (1999) Nat Genet , vol.22 , pp. 59-62
    • Rieder, M.J.1    Taylor, S.L.2    Clark, A.G.3    Nickerson, D.A.4
  • 28
    • 0035865322 scopus 로고    scopus 로고
    • A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
    • The International SNP Map Working Group
    • Sachidanandam R, Weissman D, Schmidt SC, Kakol JM, Stein LD, Marth G, Sherry S, et al (2001) A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. The International SNP Map Working Group. Nature 409:928-933
    • (2001) Nature , vol.409 , pp. 928-933
    • Sachidanandam, R.1    Weissman, D.2    Schmidt, S.C.3    Kakol, J.M.4    Stein, L.D.5    Marth, G.6    Sherry, S.7
  • 29
    • 0347358913 scopus 로고    scopus 로고
    • Opinion: The evolution of molecular markers - Just a matter of fashion?
    • Schlotterer C (2004) Opinion: the evolution of molecular markers - just a matter of fashion? Nat Rev Genet 5:63-69
    • (2004) Nat Rev Genet , vol.5 , pp. 63-69
    • Schlotterer, C.1
  • 31
    • 0032524383 scopus 로고    scopus 로고
    • Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
    • Wang DG, Fan JB, Siao CJ, Berno A, Young P, Sapolsky R, Ghandour G, et al (1998) Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. Science 280:1077-1082
    • (1998) Science , vol.280 , pp. 1077-1082
    • Wang, D.G.1    Fan, J.B.2    Siao, C.J.3    Berno, A.4    Young, P.5    Sapolsky, R.6    Ghandour, G.7
  • 32
    • 0033926575 scopus 로고    scopus 로고
    • Equivalence of single- and multilocus markers: Power to detect linkage with composite markers derived from biallelic loci
    • Wilson AF, Sorant AJ (2000) Equivalence of single- and multilocus markers: power to detect linkage with composite markers derived from biallelic loci. Am J Hum Genet 66:1610-1615
    • (2000) Am J Hum Genet , vol.66 , pp. 1610-1615
    • Wilson, A.F.1    Sorant, A.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.