利用生物学专家知识解决人类常见疾病全基因组关联研究中检测上位性的挑战

K. Pattin, J. Moore
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引用次数: 4

摘要

遗传学领域最近的技术发展产生了大量的研究工具,例如全基因组基因分型,使研究人员能够进行全基因组关联研究(GWAS),以检测增加或减少疾病易感性的遗传变异。然而,在高维数据集中发现上位性或基因-基因相互作用是一个问题,因为分析所有可能的单核苷酸多态性(snp)组合的计算复杂性。最近探索了一种解决该问题的方法,利用生物学专家知识,如途径或蛋白质-蛋白质相互作用信息,通过基于这些知识的snp选择或加权来指导分析。将评估范围缩小到在实验中显示出相互作用的基因组合,提供了一个生物学上简明的原因,为什么这两个基因可以在统计上一起被检测到。本章讨论了发现GWAS中上位相互作用的挑战,以及如何利用生物学专家知识促进全基因组遗传研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Addressing the Challenges of Detecting Epistasis in Genome-Wide Association Studies of Common Human Diseases Using Biological Expert Knowledge
Recent technological developments in the field of genetics have given rise to an abundance of research tools, such as genome-wide genotyping, that allow researchers to conduct genome-wide association studies (GWAS) for detecting genetic variants that confer increased or decreased susceptibility to disease. However, discovering epistatic, or gene-gene, interactions in high dimensional datasets is a problem due to the computational complexity that results from the analysis of all possible combinations of singlenucleotide polymorphisms (SNPs). A recently explored approach to this problem employs biological expert knowledge, such as pathway or protein-protein interaction information, to guide an analysis by the selection or weighting of SNPs based on this knowledge. Narrowing the evaluation to gene combinations that have been shown to interact experimentally provides a biologically concise reason why those two genes may be detected together statistically. This chapter discusses the challenges of discovering epistatic interactions in GWAS and how biological expert knowledge can be used to facilitate genomewide genetic studies.
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