• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Allelic frequencies and heterozygosities of microsatellite markers covering the whole genome in the Korean.

作者信息

Park M-H, Kim K-S, Lee H-J, Cho Y-M, Lee H-K, Park K-S, Shin D-J, Jang Y, Kim K-J, Jung J, Kim H-L, Oh B, Lee J-Y

机构信息

Division of Structural and Functional Genomics, Center for Genome Science, National Institute of Health, 5 Nokbun-dong, Eunpyung-gu, Seoul, 122-701, Republic of Korea.

Genome Research Center for Diabetes and Endocrine Disease, Clinical Research Institute, Seoul National University Hospital, Department of Internal Medicine, Seoul National University College of Medicine, Seoul, 110-744, South Korea.

出版信息

J Hum Genet. 2008;53(3):254-266. doi: 10.1007/s10038-008-0247-5. Epub 2008 Feb 8.

DOI:10.1007/s10038-008-0247-5
PMID:18259685
Abstract

Microsatellite markers are an essential tool for genetic linkage analysis because of their high polymorphism content. Four hundred commercially available markers covering the entire genome were genotyped from 578 sib individuals from 249 Korean families. Allelic frequencies and heterozygosities were determined for each marker loci and compared between Korean, Taiwanese, Japanese and Caucasian populations. In the three Asian populations, 10-13% of the markers had less than 0.6 heterozygosity, whereas in the Caucasian population, only 0.5% of the markers had less than 0.6 heterozygosity. Mean identical by descent (IBD) values were calculated for 578 sib individuals. Analysis of IBD values greater than 0.5 suggested that markers with low heterozygosity can also provide positive linkages, at least for the IBD sharing method of model-free linkage analysis. The data presented in this study will be a useful reference for genome-wide screens of Koreans and comparative studies with other ethnic populations.

摘要

相似文献

1
Allelic frequencies and heterozygosities of microsatellite markers covering the whole genome in the Korean.
J Hum Genet. 2008;53(3):254-266. doi: 10.1007/s10038-008-0247-5. Epub 2008 Feb 8.
2
Establishment of an optimized set of 406 microsatellite markers covering the whole genome for the Japanese population.
J Hum Genet. 2001;46(4):207-10. doi: 10.1007/s100380170090.
3
Genetic characteristics of 207 microsatellite markers in the Korean population and in other Asian populations.韩国人群及其他亚洲人群中207个微卫星标记的遗传特征。
Mol Cells. 2008 Apr 30;25(2):301-4. Epub 2008 Mar 31.
4
Heterozygosities and allelic frequencies of a set of microsatellite markers used for genome-wide scans in a Chinese population.一组用于中国人群全基因组扫描的微卫星标记的杂合性和等位基因频率。
J Hum Genet. 2002;47(11):623-31. doi: 10.1007/s100380200096.
5
Allelic frequencies of six (CA)n microsatellite markers of the dystrophin gene in the Korean population.韩国人群中抗肌萎缩蛋白基因六个(CA)n微卫星标记的等位基因频率。
Hum Hered. 1999 Jul;49(4):205-7. doi: 10.1159/000022876.
6
Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population.日本人群中358个二核苷酸重复标记位点的杂合性和等位基因频率。
J Hum Genet. 1998;43(3):165-8. doi: 10.1007/s100380050062.
7
Heterozygosities and allelic frequencies of 811 dinucleotide-repeat marker loci in the Taiwanese population.台湾人群中811个二核苷酸重复标记位点的杂合性和等位基因频率。
J Hum Genet. 2004;49(6):325-333. doi: 10.1007/s10038-004-0152-5. Epub 2004 May 19.
8
TPMD: a database and resources of microsatellite marker genotyped in Taiwanese populations.TPMD:一个对台湾人群进行微卫星标记基因分型的数据库及资源库。
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D174-7. doi: 10.1093/nar/gki102.
9
[Genetic polymorphisms of short tandem repeat loci D4S2368, D6S1043, D9S925 from Korean ethnic group of JiLin].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Oct;24(5):592-3.
10
Population data for 30 insertion-deletion markers in a Korean population.30 个插入缺失标记在韩国人群中的群体数据。
Int J Legal Med. 2014 Jan;128(1):51-2. doi: 10.1007/s00414-013-0851-6. Epub 2013 Mar 26.

引用本文的文献

1
No influence of parental origin of intact X chromosome and/or Y chromosome sequences on three-year height response to growth hormone therapy in Turner syndrome.完整的X染色体和/或Y染色体序列的亲本来源对特纳综合征患者生长激素治疗三年身高反应无影响。
Ann Pediatr Endocrinol Metab. 2014 Sep;19(3):127-34. doi: 10.6065/apem.2014.19.3.127. Epub 2014 Sep 30.

本文引用的文献

1
Heterozygosities and allelic frequencies of 811 dinucleotide-repeat marker loci in the Taiwanese population.台湾人群中811个二核苷酸重复标记位点的杂合性和等位基因频率。
J Hum Genet. 2004;49(6):325-333. doi: 10.1007/s10038-004-0152-5. Epub 2004 May 19.
2
Heterozygosities and allelic frequencies of a set of microsatellite markers used for genome-wide scans in a Chinese population.一组用于中国人群全基因组扫描的微卫星标记的杂合性和等位基因频率。
J Hum Genet. 2002;47(11):623-31. doi: 10.1007/s100380200096.
3
Analysis of 168 short tandem repeat loci in the Japanese population, using a screening set for human genetic mapping.
利用人类基因图谱筛选集对日本人群中的168个短串联重复序列位点进行分析。
J Hum Genet. 2001;46(8):448-55. doi: 10.1007/s100380170044.
4
Establishment of an optimized set of 406 microsatellite markers covering the whole genome for the Japanese population.
J Hum Genet. 2001;46(4):207-10. doi: 10.1007/s100380170090.
5
Validation of short tandem repeat analysis for the investigation of cases of disputed paternity.用于亲子鉴定案例调查的短串联重复序列分析的验证
Forensic Sci Int. 1999 Mar 15;100(1-2):1-16. doi: 10.1016/s0379-0738(98)00199-6.
6
Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population.日本人群中358个二核苷酸重复标记位点的杂合性和等位基因频率。
J Hum Genet. 1998;43(3):165-8. doi: 10.1007/s100380050062.
7
The effect of marker heterozygosity on the power to detect linkage disequilibrium.标记杂合性对检测连锁不平衡效能的影响。
Genetics. 1997 Oct;147(2):927-30. doi: 10.1093/genetics/147.2.927.
8
High resolution of human evolutionary trees with polymorphic microsatellites.利用多态微卫星实现人类进化树的高分辨率构建。
Nature. 1994 Mar 31;368(6470):455-7. doi: 10.1038/368455a0.
9
Segregation and linkage analysis.分离与连锁分析。
Anim Genet. 1992;23(1):59-62.
10
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14.14号染色体上家族性阿尔茨海默病基因座的遗传连锁证据。
Science. 1992 Oct 23;258(5082):668-71. doi: 10.1126/science.1411576.