8th International Human Genome Variation Meeting
第八届国际人类基因组变异会议
基本信息
- 批准号:7161915
- 负责人:
- 金额:$ 2万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2005
- 资助国家:美国
- 起止时间:2005-09-01 至 2007-07-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): This proposal seeks NIH funding to partially support US trainees to attend the 8th International Meeting on Human Genome Variation and Complex Genome Analysis to be held at the Le Meridien Cyberport Hotel in Hong Kong from September 14-16, 2006. This meeting is particularly timely because the field of human genome variation research is moving very fast, with the completion of the HapMap Phase I Project in October 2005 and the anticipated publication of the HapMap Phase II results in the summer of 2006. In addition, there is increasing recognition that copy number polymorphisms and structural variations of the genome are important signatures of human evolution and causes of human diseases. We will devote substantial coverage of the emerging areas of human variation research and bring together investigators in diverse fields to promote collaborations and move the field even further along. The unique feature of this meeting is that it brings together top researchers in the many areas of human variation research, from radically new technologies that will change the field dramatically, to the mechanisms of how different types of human variations came about, to new statistical approaches for genetic studies in the HapMap era, to the study of molecular evolution based on comparative genome variation analysis, and to the social and ethical implications of human variation research. The objective of the meeting is to present a three day program, which will include presentations by internationally known experts in genomics, population genetics, molecular evolution, statistical genetics, molecular epidemiology, and ethics. Sessions will be devoted to diversity and evolution, genome structure (including structural polymorphisms), population genetics, utility and analysis of haplotype maps, new variation analysis technologies and strategies, phenotype and disease, ethical, legal and social issues in human genomics.
DESCRIPTION (provided by applicant): This proposal seeks NIH funding to partially support US trainees to attend the 8th International Meeting on Human Genome Variation and Complex Genome Analysis to be held at the Le Meridien Cyberport Hotel in Hong Kong from September 14-16, 2006. This meeting is particularly timely because the field of human genome variation research is moving very fast, with the completion of the HapMap Phase I Project in October 2005 and the anticipated publication of the HAPMAP II期在2006年夏季结果。此外,人们越来越认识到,基因组的拷贝数多态性和结构变化是人类进化的重要特征和人类疾病的原因。我们将对人类变异研究的新兴领域进行大量覆盖,并将各种领域的研究人员聚集在一起,以促进合作并进一步推动该领域。 The unique feature of this meeting is that it brings together top researchers in the many areas of human variation research, from radically new technologies that will change the field dramatically, to the mechanisms of how different types of human variations came about, to new statistical approaches for genetic studies in the HapMap era, to the study of molecular evolution based on comparative genome variation analysis, and to the social and ethical implications of human variation research.会议的目的是提出一个为期三天的计划,其中包括国际知名的基因组学专家,人群遗传学,分子进化,统计遗传学,分子流行病学和伦理学的演讲。会议将致力于多样性和进化,基因组结构(包括结构性多态性),人口遗传学,单倍型图,新变异分析技术和策略,表型和疾病,人类基因组学中的伦理,法律和社会问题。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Pui-Yan KWOK其他文献
Pui-Yan KWOK的其他文献
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{{ truncateString('Pui-Yan KWOK', 18)}}的其他基金
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
基因组测序有助于儿科和产前实践中的诊断:检查不同人群的临床效用、伦理影响、付款人覆盖范围和数据整合。
- 批准号:
10359980 - 财政年份:2017
- 资助金额:
$ 2万 - 项目类别:
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
基因组测序有助于儿科和产前实践中的诊断:检查不同人群的临床效用、伦理影响、付款人覆盖范围和数据整合。
- 批准号:
9538816 - 财政年份:2017
- 资助金额:
$ 2万 - 项目类别:
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
基因组测序有助于儿科和产前实践中的诊断:检查不同人群的临床效用、伦理影响、付款人覆盖范围和数据整合。
- 批准号:
9327452 - 财政年份:2017
- 资助金额:
$ 2万 - 项目类别:
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
基因组测序有助于儿科和产前实践中的诊断:检查不同人群的临床效用、伦理影响、付款人覆盖范围和数据整合。
- 批准号:
9929780 - 财政年份:2017
- 资助金额:
$ 2万 - 项目类别:
Genomic sequencing to aid diagnosis in pediatric and prenatal practice: Examining clinical utility, ethical implications, payer coverage, and data integration in a diverse population.
基因组测序有助于儿科和产前实践中的诊断:检查不同人群的临床效用、伦理影响、付款人覆盖范围和数据整合。
- 批准号:
9926108 - 财政年份:2017
- 资助金额:
$ 2万 - 项目类别:
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
新生儿血斑 DNA 测序可改善和扩大新生儿筛查
- 批准号:
9562276 - 财政年份:2013
- 资助金额:
$ 2万 - 项目类别:
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
新生儿血斑 DNA 测序可改善和扩大新生儿筛查
- 批准号:
9105532 - 财政年份:2013
- 资助金额:
$ 2万 - 项目类别:
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
新生儿血斑 DNA 测序可改善和扩大新生儿筛查
- 批准号:
8915730 - 财政年份:2013
- 资助金额:
$ 2万 - 项目类别:
Sequencing of Newborn Blood Spot DNA to Improve and Expand Newborn Screening
新生儿血斑 DNA 测序可改善和扩大新生儿筛查
- 批准号:
9485694 - 财政年份:2013
- 资助金额:
$ 2万 - 项目类别:
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