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GWAS with AHP based SNP prioritization approach to identify SNP biomarkers for Alzheimer's disease

机译:具有基于AHP的SNP优先化方法的GWA来识别Alzheimer疾病的SNP生物标志物

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Genome wide association studies (GWAS) aim to identify genomic variance associated with certain disease conditions. Major bottleneck of standard GWAS approaches are the prioritization and subset selection after the statistically significant SNPs are determined. Our group has recently developed an analysis pipeline, where p-value and combined p value statistics are integrated with the novel AHP based SNP prioritization algorithm for the detailed analysis of associated SNPs considering statistical significance and biological relevance. Following this pipeline, we have done the GWAS of Alzheimer's Disease (AD) on ADNI SNP genotyping data set where 148 AD cases and 182 controls are investigated. Among the top 100 SNPs 18 of them mapped to AD linked genes. Additionally further analysis of the gene and pathway results suggested new associations, providing basis for new hypothesis for the AD Biomarker research.
机译:基因组宽协会研究(GWAS)旨在鉴定与某些疾病病症相关的基因组差异。 标准GWAS方法的主要瓶颈是确定统计学意义的SNP后的优先级和子集选择。 我们的小组最近开发了一个分析管道,其中P值和组合的P值统计数据与基于AHP的新型SNP优先级算法集成,用于考虑统计显着性和生物相关性的相关SNP的详细分析。 在该管道之后,我们已经在Adni SNP基因分型数据集上完成了Alzheimer疾病(AD)的Gwas,其中调查了148个AD病例和182个控制。 其中的前100名SNP 18映射到AD链接基因。 此外,进一步分析基因和途径结果建议新的协会,为广告生物标志物研究提供新假设的基础。

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