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HIGH DENSITY GENETIC MAP OF XQ25-XQ28

HIGH DENSITY GENETIC MAP OF XQ25-XQ28
XQ25-XQ28的高密度遗传图谱
批准号:
2674231
负责人:
Pui-Yan KWOK
金额:
$31.56万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1996
资助国家:
美国
项目状态:
已结题
起止时间:
1996-04-05 至 2000-03-31

项目摘要

项目成果

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中文摘要
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英文摘要
The primary goals of this project are to develop high-density genetic maps of selected regions of the human X chromosome based on well characterized physical maps and to use these maps to study linkage disequilibrium in three distinct populations. Based on extensive work performed here at the Washington University Genome Center and elsewhere, >80% of the X chromosome is covered by high quality yeast artificial chromosome (YAC) contigs. We propose to utilize this invaluable local resource and expertise to develop genetic maps with markers placed approximately 100 kb apart, using as markers single nucleotide polymorphisms that can be genotyped by the semi-automated oligonucleotide ligation assay (OLA). The use of diallelic markers, which are less mutable, is of crucial importance because the highly informative and useful simple tandem repeat polymorphism (STRP) markers appear to have a high mutation rate which make them disadvantageous for disequilibrium mapping. The regions selected comprised of 20 Mb of the X chromosome between Xq25 and Xq28. These regions contain numerous disease gene loci, including several that are of local interest. The addition of some 200 genetic markers in these regions will aid numerous investigators here and abroad in their search for their genes of interest. Once developed, the allele frequencies of these markers will be determined and they will be used to genotype approximately 100 males in each of three populations, including those of the CEPH pedigree, an isolated population in Finland, and a similarly isolated population in Sardinia. The haplotypes of these individuals will be analyzed to study linkage disequilibrium in terms of population history and chromosomal location. If successful, the approaches developed in this proposal will be applicable to any region of the human genome. Furthermore, the linkage disequilibrium data obtained will shed light on several important questions in population genetics and guide disease gene mapping efforts based on population or disequilibrium studies.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1006/geno.2000.6165
发表时间: 2000-05
期刊: Genomics
影响因子: 4.4
作者: [P. Taillon-Miller;P. Kwok]
通讯作者: P. Taillon-Miller;P. Kwok
DOI: 10.1101/gr.9.5.499
发表时间: 1999-05
期刊: Genome research
影响因子: 7
作者: [P. Taillon-Miller;E. E. Piernot-E.;P. Kwok]
通讯作者: P. Taillon-Miller;E. E. Piernot-E.;P. Kwok
海外基金