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DATA SIMULATION SOFTWARE FOR WHOLE-GENOME ASSOCIATION AND OTHER STUDIES IN HUMAN GENETICS

机译:用于人类基因组全基因组关联和其他研究的数据模拟软件

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Genome-wide association studies have become a reality in the study of the genetics of complex disease. This technology provides a wealth of genomic information on patient samples, from which we hope to learn novel biology and detect important genetic and environmental factors for disease processes. Because strategies for analyzing these data have not kept pace with the laboratory methods that generate the data it is unlikely that these advances will immediately lead to an improved understanding of the genetic contribution to common human disease and drug response. Currently, no single analytical method will allow us to extract all information from a whole-genome association study. Thus, many novel methods are being proposed and developed. It will be vital for the success of these new methods, to have the ability to simulate datasets consisting of polymorphisms throughout the genome with realistic linkage disequilibrium patterns. Within these datasets, we can embed genetic models of disease whereby we can evaluate the ability of novel methods to detect these simulated effects. This paper describes a new software package, genomeSIM, for the simulation of large-scale genomic data in population based case-control samples. It allows for single SNP, as well as gene-gene interaction models to be associated with disease risk. We describe the algorithm and demonstrate its utility for future genetic studies of whole-genome association.
机译:全基因组关联研究已成为复杂疾病遗传学研究的现实。该技术为患者样本提供了丰富的基因组信息,我们希望从中学习新颖的生物学知识并检测出疾病过程中重要的遗传和环境因素。由于分析这些数据的策略未能与生成数据的实验室方法保持同步,因此这些进展不可能立即导致人们对遗传对常见人类疾病和药物反应的贡献有所了解。当前,没有任何一种分析方法可以使我们从全基因组关联研究中提取所有信息。因此,正在提出和开发许多新颖的方法。对于这些新方法的成功至关重要的是,要能够模拟整个基因组中具有现实连锁不平衡模式的多态性数据集。在这些数据集中,我们可以嵌入疾病的遗传模型,从而可以评估新颖方法检测这些模拟效应的能力。本文介绍了一种用于模拟基于人群的病例对照样本中的大规模基因组数据的新型软件包,genericSIM。它允许单个SNP以及基因-基因相互作用模型与疾病风险相关。我们描述该算法,并证明其在全基因组关联的未来遗传学研究中的实用性。

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