中國科學院心理研究所王晶研究員課題組在全基因組關(guān)聯(lián)學習(genome-wide association study, GWAS)研究中取得重要成果,。課題組成功開發(fā)了基于通路(pathway)的GWAS數(shù)據(jù)網(wǎng)絡(luò)分析平臺——i-GSEA4GWAS,。該平臺用于鑒別與疾病表型相關(guān)的通路/基因集,以進一步研究和揭示疾病致病機理,。
全基因組關(guān)聯(lián)學習(GWAS)是一種對全基因組范圍內(nèi)的常見遺傳多態(tài)性(主要是單核苷酸多態(tài)性-single nucleotide polymorphisms, SNPs)進行總體關(guān)聯(lián)分析的方法,適用于包括精神疾?。╩ental disorder)在內(nèi)的復(fù)雜疾病的研究,。傳統(tǒng)GWAS數(shù)據(jù)分析方法對SNP/基因獨立的進行分析,忽略了復(fù)雜疾病的多基因聯(lián)合效應(yīng),。為解決上述問題,,近年來基于通路的研究原則被引入到GWAS數(shù)據(jù)分析,檢測包含多個基因的通路和性狀的關(guān)聯(lián),?;谏鲜鲇^點,王晶課題組成功研究開發(fā)了基于通路的GWAS分析方法(i-GSEA)和工具,,通過網(wǎng)絡(luò)服務(wù)的方式供世界范圍相關(guān)研究工作者使用(i-GSEA4GWAS,,URL: http://gsea4gwas.psych.ac.cn)。課題組使用i-GSEA4GWAS對一種精神疾病——雙向情感障礙(bipolar disorder)的GWAS數(shù)據(jù)進行了分析,,并發(fā)現(xiàn)了新的可能的疾病相關(guān)通路/基因集,。
該項研究得到了中國科學院心理研究所青年科學基金(O9CX115011)和北京市科學技術(shù)委員會北京市科技新星計劃(A類)(2007A082)的資助。(生物谷Bioon.com)
關(guān)于GWAS的更多閱讀
高燒的GWAS——生物谷盤點2009
Nature Genetics:發(fā)現(xiàn)牛皮癬易感基因
Nature Genetics:漢族人紅斑 狼瘡易感基因
AJHG:中國人基因差異研究
全基因組關(guān)聯(lián)分析 費力不討好,?
生物谷推薦原文出處:
Nucleic Acids Research doi:10.1093/nar/gkq324
i-GSEA4GWAS: a web server for identification of pathways/gene sets associated with traits by applying an improved gene set enrichment analysis to genome-wide association study
Kunlin Zhang, Sijia Cui, Suhua Chang, Liuyan Zhang and Jing Wang*
Genome-wide association study (GWAS) is nowadays widely used to identify genes involved in human complex disease. The standard GWAS analysis examines SNPs/genes independently and identifies only a number of the most significant SNPs. It ignores the combined effect of weaker SNPs/genes, which leads to difficulties to explore biological function and mechanism from a systems point of view. Although gene set enrichment analysis (GSEA) has been introduced to GWAS to overcome these limitations by identifying the correlation between pathways/gene sets and traits, the heavy dependence on genotype data, which is not easily available for most published GWAS investigations, has led to limited application of it. In order to perform GSEA on a simple list of GWAS SNP P-values, we implemented GSEA by using SNP label permutation. We further improved GSEA (i-GSEA) by focusing on pathways/gene sets with high proportion of significant genes. To provide researchers an open platform to analyze GWAS data, we developed the i-GSEA4GWAS (improved GSEA for GWAS) web server. i-GSEA4GWAS implements the i-GSEA approach and aims to provide new insights in complex disease studies.