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Comparing gene set analysis methods on single-nucleotide polymorphism data from Genetic Analysis Workshop 16.基于遗传分析研讨会16的单核苷酸多态性数据比较基因集分析方法。
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S96. doi: 10.1186/1753-6561-3-s7-s96.
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Integration of a priori gene set information into genome-wide association studies.将先验基因集信息整合到全基因组关联研究中。
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S95. doi: 10.1186/1753-6561-3-S7-S95.
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Integration of gene ontology pathways with North American Rheumatoid Arthritis Consortium genome-wide association data via linear modeling.通过线性建模将基因本体途径与北美类风湿性关节炎协会全基因组关联数据进行整合。
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Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study.全基因组关联研究背景下处理候选区域的不同方法的比较分析。
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Toward the identification of causal genes in complex diseases: a gene-centric joint test of significance combining genomic and transcriptomic data.迈向复杂疾病中因果基因的鉴定:一种结合基因组和转录组数据的以基因为中心的联合显著性检验。
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A pathway analysis applied to Genetic Analysis Workshop 16 genome-wide rheumatoid arthritis data.一项应用于遗传分析研讨会16全基因组类风湿性关节炎数据的通路分析。
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S91. doi: 10.1186/1753-6561-3-s7-s91.
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Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans.利用基于混合样本的全基因组关联扫描鉴定复杂疾病的易感基因。
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Gene set analyses for interpreting microarray experiments on prokaryotic organisms.用于解释原核生物微阵列实验的基因集分析。
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先验信息在全基因组关联分析中的纳入。

Inclusion of a priori information in genome-wide association analysis.

机构信息

Department of Mathematics, Hope College, Holland, Michigan 49423, USA.

出版信息

Genet Epidemiol. 2009;33 Suppl 1(Suppl 1):S74-80. doi: 10.1002/gepi.20476.

DOI:10.1002/gepi.20476
PMID:19924705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2922922/
Abstract

Genome-wide association studies (GWAS) continue to gain in popularity. To utilize the wealth of data created more effectively, a variety of methods have recently been proposed to include a priori information (e.g., biologically interpretable sets of genes, candidate gene information, or gene expression) in GWAS analysis. Six contributions to Genetic Analysis Workshop 16 Group 11 applied novel or recently proposed methods to GWAS of rheumatoid arthritis and heart disease related phenotypes. The results of these analyses were a variety of novel candidate genes and sets of genes, in addition to the validation of well-known genotype-phenotype associations. However, because many methods are relatively new, they would benefit from further methodological research to ensure that they maintain type I error rates while increasing power to find additional associations. When methods have been adapted from other study types (e.g., gene expression data analysis or linkage analysis), the lessons learned there should be used to guide implementation of techniques. Lastly, many open research questions exist concerning the logistic details of the origin of the a priori information and the way to incorporate it. Overall, our group has demonstrated a strong potential for identifying novel genotype-phenotype relationships by including a priori data in the analysis of GWAS, while also uncovering a series of questions requiring further research.

摘要

全基因组关联研究(GWAS)继续受到欢迎。为了更有效地利用所产生的大量数据,最近提出了各种方法,将先验信息(例如,具有生物学可解释性的基因集、候选基因信息或基因表达)纳入 GWAS 分析中。遗传分析研讨会 16 组 11 的六项贡献应用了新的或最近提出的方法来进行类风湿关节炎和心脏病相关表型的 GWAS。这些分析的结果除了验证众所周知的基因型-表型关联外,还包括了各种新的候选基因和基因集。然而,由于许多方法相对较新,因此需要进一步进行方法学研究,以确保它们在保持 I 型错误率的同时提高发现其他关联的能力。当方法从其他研究类型(例如,基因表达数据分析或连锁分析)中改编而来时,应从那里吸取经验教训来指导技术的实施。最后,关于先验信息的来源和纳入方式的逻辑细节存在许多悬而未决的研究问题。总的来说,我们小组通过在 GWAS 分析中纳入先验数据,展示了识别新的基因型-表型关系的强大潜力,同时也发现了一系列需要进一步研究的问题。