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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疾病/终点关联研究模型的仿真工具

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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:在全基因组关联研究(GWAS)中,单核苷酸多态性(SNP)与疾病或终点之间的关联分析已被认为是研究遗传易感性和鉴定重要生物标志物的有力策略。具有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,许多作者提出了模拟基因组领域生物数据的方法。但是,这些方法使用大规模基因组数据作为模拟实验的参考,这在无法获得特定研究数据的情况下可能会限制方法的使用。很少有方法使用实验结果或观察到的参数进行模拟。这项研究的目的是开发一个名为SITDEM的Web应用程序,以仅基于GWAS中观察到的参数,以三种不同的方法模拟疾病/终点模型。在我们的模拟中,关键任务是计算基因型的概率。基于此,我们随机抽样模拟数据。在优势模型和隐性模型中,模拟结果显示为p值对优势比或SNP相对风险的函数。我们的模拟结果显示了SITDEM在模拟基因型数据方面的潜力。 SITDEM对于调查目标SNP的观测参数之间的关系以及估算在多次比较中产生显着p值所需的变量(SNP)数量可能特别有用。拟议的仿真工具可从http://www.snpmodel.com免费获得。

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