Direct allelic variation scanning of the yeast genome

被引:291
作者
Winzeler, EA [1 ]
Richards, DR
Conway, AR
Goldstein, AL
Kalman, S
McCullough, MJ
McCusker, JH
Stevens, DA
Wodicka, L
Lockhart, DJ
Davis, RW
机构
[1] Stanford Univ, Dept Biochem, Sch Med, Stanford, CA 94305 USA
[2] Duke Univ, Med Ctr, Dept Microbiol, Durham, NC 27710 USA
[3] Stanford Univ, Dept Med, Sch Med, Stanford, CA 94305 USA
[4] Affymetrix, Santa Clara, CA 95051 USA
关键词
D O I
10.1126/science.281.5380.1194
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
As more genomes are sequenced. the identification and characterization of the causes of heritable variation within a species will be increasingly important. It is demonstrated that allelic variation in any two isolates of a species can be scanned, mapped, and scored directly and efficiently without allele-specific polymerase chain reaction. without creating new strains or constructs, and without knowing the specific nature of the variation. A total of 3714 biallelic markers, spaced about every 3.5 kilobases, were identified by analyzing the patterns obtained when total genomic DNA from two different strains of yeast was hybridized to high-density oligonucleotide arrays. The markers were then used to simultaneously map a multidrug-resistance locus and four other Loci with high resolution (11 to 64 kilobases).
引用
收藏
页码:1194 / 1197
页数:4
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