Statistical and quantitative genetics

统计和数量遗传学

• 批准号: 8796092
• 负责人: Bruce S. Weir
• 金额: $ 5.19万
• 依托单位: UNIVERSITY OF WASHINGTON
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-06-05 至 2017-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8796092
• 关键词: Alleles; Architecture; Biology; Biometry; Complex; Data; Detection; Development; Environment; Gene Expression; Genes; Genetic; Genomics; Head; Human; Individual; Institutes; Investigation; Methodology; Methods; Phenotype; Postdoctoral Fellow; Program Research Project Grants; Quantitative Genetics; Queensland; Research; Research Personnel; Resolution; Universities; Variant; Washington; Work; cohort; innovation; method development; peripheral blood; professor; programs; rare variant; statistics; trait

DESCRIPTION (provided by applicant): Five senior statistical and quantitative geneticists request Program Project support to enable them to work synergistically on the development and application of statistical methodology for the interpretation of large- scale genomic data and the characterization of the genetic architecture of complex traits. The program will be headed by Bruce Weir, Professor and Chair of Biostatistics at the University of Washington. His project is concerned with developing methodology for characterizing the associations among sets of alleles. Sharon Browning, Research Associate Professor of Biostatistics at the University of Washington, will work on methodology for the analysis of rare variant data. Greg Gibson, Professor of Biology at the Georgia Tech University, proposes an empirical investigation of rare variants with 96 gene expression traits in human peripheral blood from 2,100 individuals from four cohorts. Elizabeth Thompson, Professor of Statistics at the University of Washington, has an overall objective of the development of methods for the enhanced detection and resolution of genes contributing to complex quantitative genetic traits. Her approach will be through using dense SNP marker data for the detection and estimation of segments of gene identity by descent (ibd) shared among sets of individuals. Peter Visscher, Senior Principal Research Fellow at Queensland Institute, will develop and implement better methods to dissect trait variation and predict phenotypes from SNP and sequence data.

描述（由申请人提供）：五位高级统计和定量遗传学家请求计划项目支持，以使他们能够协同工作，开发和应用统计方法，用于解释大规模基因组数据和表征复杂性状的遗传结构。该计划将由华盛顿大学生物统计学教授兼主席布鲁斯威尔领导。他的项目涉及开发用于表征等位基因组之间关联的方法。华盛顿大学生物统计学研究副教授Sharon布朗宁将研究分析罕见变异数据的方法。格鲁吉亚理工大学生物学教授格雷格吉布森提出了一项对来自四个队列的2,100名个体的人类外周血中具有96种基因表达特征的罕见变异的实证研究。华盛顿大学统计学教授Elizabeth Thompson的总体目标是开发用于增强检测和解析有助于复杂数量遗传性状的基因的方法。她的方法将通过使用密集的SNP标记数据来检测和估计个体集合之间共享的基因同源性（ibd）片段。昆士兰州研究所的高级首席研究员Peter Visscher将开发和实施更好的方法，从SNP和序列数据中剖析性状变异并预测表型。