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GSEA-SNP 鉴定与牛副结核病相关的基因。

GSEA-SNP identifies genes associated with Johne's disease in cattle.

机构信息

Department of Animal Sciences, Washington State University, Pullman, 99164-6353, USA.

出版信息

Mamm Genome. 2010 Aug;21(7-8):419-25. doi: 10.1007/s00335-010-9278-2. Epub 2010 Aug 13.

Abstract

SNP-based gene-set enrichment analysis from single nucleotide polymorphisms, or GSEA-SNP, is a tool to identify candidate genes based on enrichment analysis of sets of genes rather than single SNP associations. The objective of this study was to identify modest-effect genes associated with Mycobacterium avium subsp. paratuberculosis (Map) tissue infection or fecal shedding using GSEA-SNP applied to KEGG pathways or Gene Ontology (GO) gene sets. The Illumina Bovine SNP50 BeadChip was used to genotype 209 Holstein cows for the GSEA-SNP analyses. For each of 13,744 annotated genes genome-wide located within 50 kb of a Bovine SNP50 SNP, the single SNP with the highest Cochran-Armitage Max statistic was used as a proxy statistic for that gene's strength of affiliation with Map. Gene-set enrichment was tested using a weighted Kolmogorov-Smirnov-like running sum statistic with data permutation to adjust for multiple testing. For tissue infection and fecal shedding, no gene sets in KEGG pathways or in GO sets for molecular function or cellular component were enriched for signal. The GO biological process gene set for positive regulation of cell motion (GO:0051272, q = 0.039, 5/11 genes contributing to the core enrichment) was enriched for Map tissue infection, while no GO biological process gene sets were enriched for fecal shedding. GSEA-SNP complements traditional SNP association approaches to identify genes of modest effects as well as genes with larger effects as demonstrated by the identification of one locus that we previously found to be associated with Map tissue infection using a SNP-by-SNP genome-wide association study.

摘要

基于单核苷酸多态性的基因集富集分析(GSEA-SNP)是一种基于基因集富集分析而非单个 SNP 关联来识别候选基因的工具。本研究的目的是利用 GSEA-SNP 对 KEGG 通路或基因本体论(GO)基因集进行富集分析,鉴定与禽分枝杆菌副结核亚种(Map)组织感染或粪便脱落相关的中等效应基因。Illumina Bovine SNP50 BeadChip 用于对 209 头荷斯坦奶牛进行 GSEA-SNP 分析的基因分型。对于位于 Bovine SNP50 SNP 50kb 范围内的 13744 个注释基因中的每一个,使用 Cochran-Armitage Max 统计量最高的单个 SNP 作为该基因与 Map 关联强度的代理统计量。使用加权 Kolmogorov-Smirnov 似然运行和数据置换总和统计量来检验基因集的富集,以调整多重检验。对于组织感染和粪便脱落,KEGG 通路或分子功能或细胞成分的 GO 集都没有富集信号。GO 生物过程中对细胞运动的正向调节基因集(GO:0051272,q = 0.039,5/11 个基因对核心富集有贡献)与 Map 组织感染富集,而粪便脱落没有富集的 GO 生物过程基因集。GSEA-SNP 补充了传统的 SNP 关联方法,可以识别具有中等效应的基因,以及具有较大效应的基因,正如我们之前使用 SNP-by-SNP 全基因组关联研究发现与 Map 组织感染相关的一个基因座所证明的那样。

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