Literature DB >> 24480173

SITDEM: a simulation tool for disease/endpoint models of association studies based on single nucleotide polymorphism genotypes.

Jung Hun Oh1, Joseph O Deasy2.   

Abstract

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.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Biomarker; GWAS; Genotype; SNP

Mesh:

Substances:

Year:  2013        PMID: 24480173      PMCID: PMC4784426          DOI: 10.1016/j.compbiomed.2013.11.021

Source DB:  PubMed          Journal:  Comput Biol Med        ISSN: 0010-4825            Impact factor:   4.589


  24 in total

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3.  MLR-tagging: informative SNP selection for unphased genotypes based on multiple linear regression.

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4.  GWAsimulator: a rapid whole-genome simulation program.

Authors:  Chun Li; Mingyao Li
Journal:  Bioinformatics       Date:  2007-11-15       Impact factor: 6.937

5.  When to use the odds ratio or the relative risk?

Authors:  Carsten Oliver Schmidt; Thomas Kohlmann
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6.  Q&A: promise and pitfalls of genome-wide association studies.

Authors:  John F Y Brookfield
Journal:  BMC Biol       Date:  2010-04-12       Impact factor: 7.431

7.  Genetic variation in coding regions between and within commonly used inbred rat strains.

Authors:  Bart M G Smits; Bert F M van Zutphen; Ronald H A Plasterk; Edwin Cuppen
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Review 8.  Genomewide association studies: history, rationale, and prospects for psychiatric disorders.

Authors:  Sven Cichon; Nick Craddock; Mark Daly; Stephen V Faraone; Pablo V Gejman; John Kelsoe; Thomas Lehner; Douglas F Levinson; Audra Moran; Pamela Sklar; Patrick F Sullivan
Journal:  Am J Psychiatry       Date:  2009-04-01       Impact factor: 18.112

9.  A unified framework for multi-locus association analysis of both common and rare variants.

Authors:  Daniel Shriner; Laura Kelly Vaughan
Journal:  BMC Genomics       Date:  2011-01-31       Impact factor: 3.969

10.  Generating samples for association studies based on HapMap data.

Authors:  Jing Li; Yixuan Chen
Journal:  BMC Bioinformatics       Date:  2008-01-24       Impact factor: 3.169

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  1 in total

1.  Computational methods using genome-wide association studies to predict radiotherapy complications and to identify correlative molecular processes.

Authors:  Jung Hun Oh; Sarah Kerns; Harry Ostrer; Simon N Powell; Barry Rosenstein; Joseph O Deasy
Journal:  Sci Rep       Date:  2017-02-24       Impact factor: 4.379

  1 in total

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