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基因表达数据的多结果荟萃分析方法。

Methods for multiple outcome meta-analysis of gene-expression data.

作者信息

Vennou Konstantina E, Piovani Daniele, Kontou Panagiota I, Bonovas Stefanos, Bagos Pantelis G

机构信息

Department of Computer Science and Biomedical Informatics, University of Thessaly, Lamia 35131, Greece.

Department of Biomedical Sciences, Humanitas University, Milan, Italy.

出版信息

MethodsX. 2020 Feb 21;7:100834. doi: 10.1016/j.mex.2020.100834. eCollection 2020.

DOI:10.1016/j.mex.2020.100834
PMID:32195147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7078352/
Abstract

Meta-analysis is a valuable tool for the synthesis of evidence across a wide range study types including high-throughput experiments such as genome-wide association studies (GWAS) and gene expression studies. There are situations though, in which we have multiple outcomes or multiple treatments, in which the multivariate meta-analysis framework which performs a joint modeling of the different quantities of interest may offer important advantages, such as increasing statistical power and allowing performing global tests. In this work we adapted the multivariate meta-analysis method and applied it in gene expression data. With this method we can test for pleiotropic effects, that is, for genes that influence both outcomes or discover genes that have a change in expression not detectable in the univariate method. We tested this method on data regarding inflammatory bowel disease (IBD), with its two main forms, Crohn's disease (CD) and Ulcerative colitis (UC), sharing many clinical manifestations, but differing in the location and extent of inflammation and in complications. The Stata code is given in the Appendix and it is available at: www.compgen.org/tools/multivariate-microarrays.•Multivariate meta-analysis method for gene expression data.•Discover genes with pleiotropic effects.•Differentially Expressed Genes (DEGs) identification in complex traits.

摘要

荟萃分析是一种用于综合多种研究类型证据的重要工具,这些研究类型包括高通量实验,如全基因组关联研究(GWAS)和基因表达研究。然而,在某些情况下,我们会遇到多个结局或多种治疗方法,此时多变量荟萃分析框架对不同感兴趣量进行联合建模可能会带来重要优势,比如提高统计功效并允许进行全局检验。在这项工作中,我们对多变量荟萃分析方法进行了调整,并将其应用于基因表达数据。通过这种方法,我们可以检测基因的多效性,即那些影响多个结局的基因,或者发现单变量方法无法检测到表达变化的基因。我们在关于炎症性肠病(IBD)的数据上测试了这种方法,IBD有两种主要形式,克罗恩病(CD)和溃疡性结肠炎(UC),它们有许多共同的临床表现,但在炎症的位置和范围以及并发症方面存在差异。附录中给出了Stata代码,可在以下网址获取:www.compgen.org/tools/multivariate-microarrays。

•基因表达数据的多变量荟萃分析方法。

•发现具有多效性的基因。

•复杂性状中差异表达基因(DEG)的鉴定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d1/7078352/a6c563702663/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d1/7078352/a6c563702663/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18d1/7078352/a6c563702663/fx1.jpg

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本文引用的文献

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Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus.儿童肌肉骨骼特征的双变量全基因组关联荟萃分析揭示了SREBF1/TOM1L2基因座的多效性作用。
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