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Reconstructability analysis of genetic loci associated with Alzheimer disease

机译:阿尔茨海默氏病相关基因位点的可重构性分析

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Reconstructability Analysis (RA) is an information- and graph-theory-based method which has been successfully used in previous genomic studies. Here we apply it to genetic (14 SNPs) and non-genetic (Education, Age, Gender) data on Alzheimer disease in a well-characterized Case/Control sample of 424 individuals. We confirm the importance of APOE as a predictor of the disease, and identify one non-genetic factor, Education, and two SNPs, one in BINI and the other in SORCS1, as likely disease predictors. SORCS1 appears to be a common risk factor for people with or without APOE. We also identify a possible interaction effect between Education and BINI. Methodologically, we introduce and use to advantage some more powerful features of RA not used in prior genomic studies.
机译:可重构性分析(RA)是一种基于信息和图论的方法,已在以前的基因组研究中成功使用。在这里,我们将其应用于424个个体的典型病例/对照样本中有关阿尔茨海默氏病的遗传(14个SNP)和非遗传(教育,年龄,性别)数据。我们确认APOE作为疾病预测因子的重要性,并确定一种非遗传因素,教育和两个SNP(可能在疾病预测因子中使用,一种在BINI中,另一种在SORCS1中)。对于有或没有APOE的人,SORCS1似乎是常见的危险因素。我们还确定了教育与BINI之间可能的交互作用。从方法上讲,我们介绍并利用了先前基因组研究中未使用过的RA的一些更强大的功能。

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