人类基因关联研究:人类基因组与临床结果的关系

F. Khatoon
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引用次数: 2

摘要

使用全基因组关联研究来检测法医感兴趣的许多疾病,性别分布的特征是由于患病率的性别相关差异[1]。性别和祖先相关数据和遗传信息是GWAS中数量检查(QC)的重要组成部分,可以在实践中实施,以消除样本的错误识别和群体样本的分层。如果观察到的表型是由研究中每个受试者的观察到的基因型引起的,那么在检测到基因型和表型特征之间存在强烈关联的过程中,可以推断出识别错误的方法[2]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human Genetic Association Studies: association between of Human genome with Clinical outcome
The use of Genome Wide Association Studies for detecting many diseases of forensic interest and traits for sex distributions are due to sex associated variations in prevalence [1]. The sex and ancestry related data and genetic information are important components for Quantity Check (QC) in GWAS and can be implemented in practice to remove misidentifications of samples and stratifications in population samples. The approach to identify the mis-identification in processes where strong associations are detected between genotype and phenotype characteristics can be inferred if the observed phenotype is expected to be caused by the observed genotype for every subject within the study[2].
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