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首页> 外文期刊>Computers in Biology and Medicine >SITDEM: A simulation tool for disease/endpoint models of association studies based on single nucleotide polymorphism genotypes
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SITDEM: A simulation tool for disease/endpoint models of association studies based on single nucleotide polymorphism genotypes

机译:SitDem:基于单核苷酸多态性基因型的关联研究疾病/终点模型的模拟工具

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摘要

The association analysis between single nucleotide polymorphisms (SNPs) and disease or endpoint in genome-wide association studies (GWAS) has been considered as a powerful strategy for investigating genetic susceptibility and for identifying significant biomarkers. The statistical analysis approaches with simulated data have been widely used to review experimental designs and performance measurements. In recent years, a number of authors have proposed methods for the simulation of biological data in the genomic field. However, these methods use large-scale genomic data as a reference to simulate experiments, which may limit the use of the methods in the case where the data in specific studies are not available. Few methods use experimental results or observed parameters for simulation. The goal of this study is to develop a Web application called SITDEM to simulate disease/endpoint models in three different approaches based on only parameters observed in GWAS. In our simulation, a key task is to compute the probability of genotypes. Based on that, we randomly sample simulation data. Simulation results are shown as a function of p-value against odds ratio or relative risk of a SNP in dominant and recessive models. Our simulation results show the potential of SITDEM for simulating genotype data. SITDEM could be particularly useful for investigating the relationship among observed parameters for target SNPs and for estimating the number of variables (SNPs) required to result in significant p-values in multiple comparisons. The proposed simulation tool is freely available at http://www.snpmodel.com.
机译:单一核苷酸多态性(SNP)和疾病或终点之间的关联分析或基因组关联研究(GWAs)被认为是调查遗传易感性和识别重要生物标志物的强大策略。模拟数据的统计分析方法已被广泛用于审查实验设计和性能测量。近年来,许多作者已经提出了用于模拟基因组领域生物数据的方法。然而,这些方法使用大规模的基因组数据作为模拟实验的参考,这可能限制在特定研究中数据的情况下的方法使用。少数方法使用实验结果或观察到的仿真参数。本研究的目标是开发一个名为SITDEM的Web应用程序,以模拟三种不同方法的疾病/端点模型,基于GWAS中观察到的参数。在我们的模拟中,关键任务是计算基因型的概率。基于此,我们随机采样模拟数据。仿真结果显示为P值的函数,抵抗占主导地位和隐性模型中SNP的差距或相对风险的函数。我们的仿真结果表明了SITDEM用于模拟基因型数据的潜力。 SITDEM对于调查目标SNP的观察参数的关系特别有用,并且用于估计在多种比较中导致显着的p值所需的变量(SNP)的数量。拟议的仿真工具可在http://www.snpmodel.com自由提供。

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