...
首页> 外文期刊>BMC Genomics >Investigation of multi-trait associations using pathway-based analysis of GWAS summary statistics
【24h】

Investigation of multi-trait associations using pathway-based analysis of GWAS summary statistics

机译:基于GWAS汇总统计的途径分析对多特征缔协会的研究

获取原文
           

摘要

Genome-wide association studies (GWAS) have been successful in identifying disease-associated genetic variants. Recently, an increasing number of GWAS summary statistics have been made available to the research community, providing extensive repositories for studies of human complex diseases. In particular, cross-trait associations at the genetic level can be beneficial from large-scale GWAS summary statistics by using genetic variants that are associated with multiple traits. However, direct assessment of cross-trait associations using susceptibility loci has been challenging due to the complex genetic architectures in most diseases, calling for advantageous methods that could integrate functional interpretation and imply biological mechanisms. We developed an analytical framework for systematic integration of cross-trait associations. It incorporates two different approaches to detect enriched pathways and requires only summary statistics. We demonstrated the framework using 25 traits belonging to four phenotype groups. Our results revealed an average of 54 significantly associated pathways (ranged between 18 and 175) per trait. We further proved that pathway-based analysis provided increased power to estimate cross-trait associations compared to gene-level analysis. Based on Fisher's Exact Test (FET), we identified a total of 24 (53) pairs of trait-trait association at adjusted pFET??1?×?10-?3 (pFET??0.01) among the 25 traits. Our trait-trait association network revealed not only many relationships among the traits within the same group but also novel relationships among traits from different groups, which warrants further investigation in future. Our study revealed that risk variants for 25 different traits aggregated in particular biological pathways and that these pathways were frequently shared among traits. Our results confirmed known mechanisms and also suggested several novel insights into the etiology of multi-traits.
机译:基因组 - 范围协会研究(GWAs)已经成功地鉴定疾病相关的遗传变异。最近,已经向研究界提供了越来越多的GWAS汇总统计数据,为人类复杂疾病的研究提供了广泛的储存库。特别地,遗传水平的交叉特征缔协会可以通过使用与多种性状相关的遗传变异来源于大规模的GWAS概要统计。然而,由于大多数疾病中的复杂遗传架构,直接评估使用易感性基因座的交叉特征缔约方协会一直挑战,呼吁可以​​整合功能解释和意味着生物机制的有利方法。我们开发了一个分析框架,用于系统地集成交叉特征联想。它包含两种不同的方法来检测丰富的途径,只需要概要统计数据。我们使用属于四种表型组的25个特征展示了该框架。我们的结果平均揭示了每种特征的54例明显相关的途径(18至175岁之间)。我们进一步证明了基于途径的分析提供了与基因水平分析相比估计交叉特性联想的增加。基于Fisher的精确测试(FET),我们在调整后的PFET中鉴定了总共24(53)对特征结合?<?1?×10-?3(PFET?<0.01)在25个特征中。我们的特质交易网络不仅揭示了同一组织内的特征之间的许多关系,而且还有新的不同群体的特征关系,这是未来进一步调查的。我们的研究表明,25种不同性状的风险变体在特定的生物途径中聚集,并且这些途径经常在特征中共享。我们的结果证实了已知的机制,并提出了几个新颖的洞察多特性的病因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号