High throughput analysis of 10 microsatellite and 11 diallelic polymorphisms on the human Y-chromosome

被引:79
作者
Thomas, MG
Bradman, N
Flinn, HM
机构
[1] UCL, Ctr Genet Anthropol, London WC1E 6BT, England
[2] UCL, Dept Anthropol, London WC1E 6BT, England
[3] UCL, Dept Biol, London WC1E 6BT, England
关键词
D O I
10.1007/s004390051148
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe an integrated approach to the determination of complex Y chromosome haplotypes that is both fast and relatively inexpensive. The method employs GeneScan technology to enable a researcher to assay repeat number variation at ten microsatellite loci and determine the status of 11 diallelic polymorphisms. The method requires only four PCRs and four GeneScan runs per sample and is relatively insensitive to sample DNA concentration.
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页码:577 / 581
页数:5
相关论文
共 16 条
  • [1] RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS
    BOOM, R
    SOL, CJA
    SALIMANS, MMM
    JANSEN, CL
    WERTHEIMVANDILLEN, PME
    VANDERNOORDAA, J
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) : 495 - 503
  • [2] FAERMAN M, 1999, IN PRESS AM J PHYSL
  • [3] HAMMER MF, 1994, MOL BIOL EVOL, V11, P749
  • [4] Out of Africa and back again: Nested cladistic analysis of human Y chromosome variation
    Hammer, MF
    Karafet, T
    Rasanayagam, A
    Wood, ET
    Altheide, TK
    Jenkins, T
    Griffiths, RC
    Templeton, AR
    Zegura, SL
    [J]. MOLECULAR BIOLOGY AND EVOLUTION, 1998, 15 (04) : 427 - 441
  • [5] Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal males
    Jobling, MA
    Samara, V
    Pandya, A
    Fretwell, N
    Bernasconi, B
    Mitchell, RJ
    Gerelsaikhan, T
    Dashnyam, B
    Sajantila, A
    Salo, PJ
    Nakahori, Y
    Disteche, CM
    Thangaraj, K
    Singh, L
    Crawford, MH
    TylerSmith, C
    [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (11) : 1767 - 1775
  • [6] Evaluation of Y-chromosomal STRs: A multicenter study
    Kayser, M
    Caglia, A
    Corach, D
    Fretwell, N
    Gehrig, C
    Graziosi, G
    Heidorn, F
    Herrmann, S
    Herzog, B
    Hidding, M
    Honda, K
    Jobling, M
    Krawczak, M
    Leim, K
    Meuser, S
    Meyer, E
    Oesterreich, W
    Pandya, A
    Parson, W
    Penacino, G
    PerezLezaun, A
    Piccinini, A
    Prinz, M
    Schmitt, C
    Schneider, PM
    Szibor, R
    TeifelGreding, J
    Weichold, G
    deKnijff, P
    Roewer, L
    [J]. INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 1997, 110 (03) : 125 - +
  • [7] Dual origins of Finns revealed by Y chromosome haplotype variation
    Kittles, RA
    Perola, M
    Peltonen, L
    Bergen, AW
    Aragon, RA
    Virkkunen, M
    Linnoila, M
    Goldman, D
    Long, JC
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) : 1171 - 1179
  • [8] HIGHLY INFORMATIVE COMPOUND HAPLOTYPES FOR THE HUMAN Y-CHROMOSOME
    MATHIAS, N
    BAYES, M
    TYLERSMITH, C
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (01) : 115 - 123
  • [9] Redd AJ, 1997, BIOL CHEM, V378, P923
  • [10] Analysis of molecular variance (AMOVA) of Y-chromosome-specific microsatellites in two closely related human populations
    Roewer, L
    Kayser, M
    Dieltjes, P
    Nagy, M
    Bakker, E
    Krawczak, M
    deKnijff, P
    [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (07) : 1029 - 1033