Pattern and Process in Human DNA Sequence Variation
人类 DNA 序列变异的模式和过程
基本信息
- 批准号:0850997
- 负责人:
- 金额:$ 26.53万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Standard Grant
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-09-01 至 2013-08-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
This research will contrast and test two competing views about human genetic diversity and evolution. One view sees our genetic diversity as the outcome of founder effects that occurred as the human species expanded from Africa and filled the rest of the globe. The other view sees our genetic diversity as the outcome of genetic drift in a vast network of stable populations connected by local gene flow. To resolve these opposing views, this project will collect new DNA sequence data, and it will conduct analyses in a novel quantitative framework that is built from stochastic population genetic models. The intellectual merit of this project is that it uses a specific research design to resolve long-standing questions about human evolution and diversity. It uses the alternative scenarios for human evolution to make precise numerical predictions about patterns of DNA sequence differences. To test these predictions, the project will collect new data that are directly relevant to the questions at hand. The project's broader impact on the scientific community has several dimensions. It will produce a new body of DNA sequence data, and it will make these data publicly available in GenBank. It will develop new statistical tools that the principal investigator will distribute to other researchers free of charge. The project has a training component that will fuse the talents of graduate students with those of undergraduates. Students at both levels will help conduct the research and participate in analyses and reports. The principal investigator will use the results of this research to write an article for lay audiences on the topic of diversity and race in light of modern genomics. This article will explain to the lay public how human evolution provides a new nonracial framework to understand human differences and likeness.
这项研究将对比和检验关于人类遗传多样性和进化的两种相互竞争的观点。一种观点认为,我们的基因多样性是创始人效应的结果,这种效应发生在人类物种从非洲扩张到全球其他地方时。另一种观点认为,我们的遗传多样性是由当地基因流连接的稳定种群组成的庞大网络中遗传漂移的结果。为了解决这些对立的观点,该项目将收集新的DNA序列数据,并将在一个由随机种群遗传模型建立的新的量化框架中进行分析。这个项目的学术价值在于,它使用了一种特定的研究设计来解决关于人类进化和多样性的长期存在的问题。它使用人类进化的其他场景来对DNA序列差异的模式做出精确的数字预测。为了验证这些预测,该项目将收集与手头问题直接相关的新数据。该项目对科学界的更广泛影响有几个方面。它将产生一个新的DNA序列数据体,并将在GenBank中公开这些数据。它将开发新的统计工具,首席研究员将免费分发给其他研究人员。该项目有一个培训部分,将把研究生和本科生的才华融合在一起。两个级别的学生都将帮助进行研究,并参与分析和报告。首席研究员将利用这项研究的结果,根据现代基因组学为非专业读者撰写一篇关于多样性和种族主题的文章。这篇文章将向公众解释人类进化如何提供了一个新的非种族框架来理解人类的差异和相似之处。
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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Jeffrey Long其他文献
Who We Are and How We Got Here: Ancient DNA and the New Science of the Human Past, by David Reich
我们是谁以及我们如何来到这里:古代 DNA 和人类过去的新科学,作者:David Reich
- DOI:
- 发表时间:
2017 - 期刊:
- 影响因子:0
- 作者:
Jeffrey Long - 通讯作者:
Jeffrey Long
God’s characteristics as reported by near-death experiencers
濒死体验者所报告的上帝特征
- DOI:
10.32388/2ti1t7 - 发表时间:
2023 - 期刊:
- 影响因子:0
- 作者:
Patrizio E. Tressoldi;Jeffrey Long - 通讯作者:
Jeffrey Long
118. Feasibility and Accuracy of the Asert Digital Questionnaire in Mood Tracking for a Research Study on Bipolar Disorder: A 6-Month Update
118. 用于双相情感障碍研究中情绪追踪的Asert数字问卷的可行性和准确性:6个月的最新情况
- DOI:
10.1016/j.biopsych.2025.02.355 - 发表时间:
2025-05-01 - 期刊:
- 影响因子:9.000
- 作者:
Isaac Lynch;Gail Harmata;John Barsotti;Jess Fiedorowicz;Aislinn Williams;Cari Linkenmeyer;Sarah Smith;Spencer Smith;Jenny Gringer Richards;Jeffrey Long;Soňa Sikorová;Eduard Bakstein;John Wemmie;Vincent Magnotta - 通讯作者:
Vincent Magnotta
Administration of the steroid marinobufagenin (MBG) mimics Salt-Sensitive hypertension in Dahl-S, but not in normotensive Sprague-Dawley rats
- DOI:
10.1016/j.jash.2016.03.025 - 发表时间:
2016-04-01 - 期刊:
- 影响因子:
- 作者:
Olga V. Fedorova;Yulia N. Grigorova;Mikayla L. Hall;Ondrej Juhasz;Wen Wei;Natalia Petrashevskaya;Valentina I. Zernetkina;Jeffrey Long;Kenneth W. Fishbein;Peter R. Rapp;Richard G. Spencer;Edward G. Lakatta;Alexei Y. Bagrov - 通讯作者:
Alexei Y. Bagrov
Association of blood pressure and na-pump inhibitor marinobufagenin (MBG) with brain structure, assessed by <em>in vivo</em> MRI in Sprague-Dawley and Dahl-S Rats
- DOI:
10.1016/j.jash.2016.03.145 - 发表时间:
2016-04-01 - 期刊:
- 影响因子:
- 作者:
Olga V. Fedorova;Mikayla L. Hall;Kenneth W. Fishbein;Yulia N. Grigovora;Mustafa Bouhrara;Wen Wei;Jeffrey Long;Christopher A. Morrell;Peter P. Rapp;Edward G. Lakatta;Richard G. Spencer;Alexei Y. Bagrov - 通讯作者:
Alexei Y. Bagrov
Jeffrey Long的其他文献
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{{ truncateString('Jeffrey Long', 18)}}的其他基金
A Coordination Chemistry Approach to the Synthesis of Single-Molecule Magnets
合成单分子磁体的配位化学方法
- 批准号:
2350466 - 财政年份:2024
- 资助金额:
$ 26.53万 - 项目类别:
Continuing Grant
CAS: Hard Permanent Magnets Through Molecular Design
CAS:通过分子设计实现硬质永磁体
- 批准号:
2206534 - 财政年份:2022
- 资助金额:
$ 26.53万 - 项目类别:
Continuing Grant
A Coordination Chemistry Approach to the Synthesis of Single- Molecule Magnets
合成单分子磁体的配位化学方法
- 批准号:
2102603 - 财政年份:2021
- 资助金额:
$ 26.53万 - 项目类别:
Continuing Grant
A Coordination Chemistry Approach to the Synthesis of Single-Molecule Magnets
合成单分子磁体的配位化学方法
- 批准号:
1800252 - 财政年份:2018
- 资助金额:
$ 26.53万 - 项目类别:
Continuing Grant
A Coordination Chemistry Approach to the Synthesis of Single-Molecule Magnets
合成单分子磁体的配位化学方法
- 批准号:
1464841 - 财政年份:2015
- 资助金额:
$ 26.53万 - 项目类别:
Standard Grant
Repression Mediated Embryonic Paterning in Arabidopsis
拟南芥中抑制介导的胚胎模式
- 批准号:
1457381 - 财政年份:2015
- 资助金额:
$ 26.53万 - 项目类别:
Continuing Grant
I-Corps: The Commercialization Potential of Pyrazolate Metal-Organic Frameworks (MOFs)
I-Corps:吡唑盐金属有机框架(MOF)的商业化潜力
- 批准号:
1508127 - 财政年份:2014
- 资助金额:
$ 26.53万 - 项目类别:
Standard Grant
A Coordination Chemistry Approach to the Synthesis of Single-Molecule Magnets
合成单分子磁体的配位化学方法
- 批准号:
1111900 - 财政年份:2011
- 资助金额:
$ 26.53万 - 项目类别:
Standard Grant
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