High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

被引:408
作者
Buetow, KH [1 ]
Edmonson, M
MacDonald, R
Clifford, R
Yip, P
Kelley, J
Little, DP
Strausberg, R
Koester, H
Cantor, CR
Braun, A
机构
[1] NCI, Lab Populat Genet, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[2] NCI, Off Genom, Bethesda, MD 20892 USA
[3] Sequenom Inc, San Diego, CA 92121 USA
关键词
D O I
10.1073/pnas.021506298
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We describe here a system for the rapid identification, assay development, and characterization of gene-based single nucleotide polymorphisms (SNPs). This system couples informatics tools that mine candidate SNPs from public expressed sequence tag resources and automatically designs assay reagents with detection by a chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry platform. As a proof of concept of this system, a genomewide collection of reagents for 9,115 gene-based SNP genetic markers was rapidly developed and validated. These data provide preliminary insights into patterns of polymorphism in a genomewide collection of gene-based polymorphisms.
引用
收藏
页码:581 / 584
页数:4
相关论文
共 11 条
[1]  
Braun A, 1997, CLIN CHEM, V43, P1151
[2]  
Dal YQ, 1996, RAPID COMMUN MASS SP, V10, P1792, DOI 10.1002/(SICI)1097-0231(199611)10:14<1792::AID-RCM753>3.0.CO
[3]  
2-N
[4]   PROGRAM DESCRIPTION - CENTER-DETUDE-DU-POLYMORPHISME-HUMAIN (CEPH) - COLLABORATIVE GENETIC-MAPPING OF THE HUMAN GENOME [J].
DAUSSET, J ;
CANN, H ;
COHEN, D ;
LATHROP, M ;
LALOUEL, JM ;
WHITE, R .
GENOMICS, 1990, 6 (03) :575-577
[5]   A physical map of 30,000 human genes [J].
Deloukas, P ;
Schuler, GD ;
Gyapay, G ;
Beasley, EM ;
Soderlund, C ;
Rodriguez-Tomé, P ;
Hui, L ;
Matise, TC ;
McKusick, KB ;
Beckmann, JS ;
Bentolila, S ;
Bihoreau, MT ;
Birren, BB ;
Browne, J ;
Butler, A ;
Castle, AB ;
Chiannilkulchai, N ;
Clee, C ;
Day, PJR ;
Dehejia, A ;
Dibling, T ;
Drouot, N ;
Duprat, S ;
Fizames, C ;
Fox, S ;
Gelling, S ;
Green, L ;
Harrison, P ;
Hocking, R ;
Holloway, E ;
Hunt, S ;
Keil, S ;
Lijnzaad, P ;
Louis-Dit-Sully, C ;
Ma, J ;
Mendis, A ;
Miller, J ;
Morissette, J ;
Muselet, D ;
Nusbaum, HC ;
Peck, A ;
Rozen, S ;
Simon, D ;
Slonim, DK ;
Staples, R ;
Stein, LD ;
Stewart, EA ;
Suchard, MA ;
Thangarajah, T ;
Vega-Czarny, N .
SCIENCE, 1998, 282 (5389) :744-746
[6]   Generation and analysis of 280,000 human expressed sequence tags [J].
Hillier, L ;
Lennon, G ;
Becker, M ;
Bonaldo, MF ;
Chiapelli, B ;
Chissoe, S ;
Dietrich, N ;
DuBuque, T ;
Favello, A ;
Gish, W ;
Hawkins, M ;
Hultman, M ;
Kucaba, T ;
Lacy, M ;
Le, M ;
Le, N ;
Mardis, E ;
Moore, B ;
Morris, M ;
Parsons, J ;
Prange, C ;
Rifkin, L ;
Rohlfing, T ;
Schellenberg, K ;
Soares, MB ;
Tan, F ;
ThierryMeg, J ;
Trevaskis, E ;
Underwood, K ;
Wohldman, P ;
Waterston, R ;
Wilson, R ;
Marra, M .
GENOME RESEARCH, 1996, 6 (09) :807-828
[7]   Polymorphism in the coagulation factor VII gene and the risk of myocardial infarction [J].
Iacoviello, L ;
Di Castelnuovo, A ;
de Knijff, P ;
D'Orazio, A ;
Amore, C ;
Arboretti, R ;
Kluft, C ;
Donati, MB .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (02) :79-85
[8]  
Little DP, 1997, EUR J CLIN CHEM CLIN, V35, P545
[9]   Mass spectrometry from miniaturized arrays for full comparative DNA analysis [J].
Little, DP ;
Braun, A ;
O'Donnell, MJ ;
Köster, H .
NATURE MEDICINE, 1997, 3 (12) :1413-1416
[10]   The future of genetic studies of complex human diseases [J].
Risch, N ;
Merikangas, K .
SCIENCE, 1996, 273 (5281) :1516-1517