Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

被引:188
作者
Wiltshire, T [1 ]
Pletcher, MT
Batalov, S
Barnes, SW
Tarantino, LM
Cooke, MP
Wu, H
Smylie, K
Santrosyan, A
Copeland, NG
Jenkins, NA
Kalush, F
Mural, RJ
Glynne, RJ
Kay, SA
Adams, MD
Fletcher, CF
机构
[1] Novartis Res Fdn, Genom Inst, San Diego, CA 92121 USA
[2] Scripps Res Inst, San Diego, CA 92121 USA
[3] Phenomix, San Diego, CA 92121 USA
[4] Seqeunom Inc, San Diego, CA 92121 USA
[5] NCI, Frederick, MD 21702 USA
[6] Celera Genom, Rockville, MD 20850 USA
关键词
D O I
10.1073/pnas.0130101100
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
The nature and organization of polymorphisms, or differences, between genomes of individuals are of great interest, because these variations can be associated with or even underlie phenotypic traits, including disease susceptibility. To gain insight into the genetic and evolutionary factors influencing such biological variation, we have examined the arrangement (haplotype) of single-nucleotide polymorphisms across the genomes of eight inbred strains of mice. These analyses define blocks of high or low diversity, often extending across tens of megabases that are delineated by abrupt transitions. These observations provide a striking contrast to the haplotype structure of the human genome.
引用
收藏
页码:3380 / 3385
页数:6
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