PCA-based GRS analysis enhances the effectiveness for genetic correlation detection. (29th August 2018)

• Record Type: Journal Article
• Authors: Zhao, Yan; Ning, Yujie; Zhang, Feng; Ding, Miao; Wen, Yan; Shi, Liang; Wang, Kunpeng; Lu, Mengnan; Sun, Jingyan; Wu, Menglu; Cheng, Bolun; Ma, Mei; Zhang, Lu; Cheng, Shiqiang; Shen, Hui; Tian, Qing; Guo, Xiong; Deng, Hong-Wen
• Is Part Of: Briefings in bioinformatics. Volume 20:Number 6(2020)
• Page Start: 2291
• Page End: 2298
• Publication Date: 2018-08-29
• Subjects: bioinformatics -- principal component analysis -- genetic risk score -- correlation analysis -- complex diseases; Genetics -- Data processing -- Periodicals; Molecular biology -- Data processing -- Periodicals; Genomes -- Data processing -- Periodicals; 572.80285
• DOI: 10.1093/bib/bby075
• Languages: English
• ISSNs: 1467-5463

Abstract

Abstract: Genetic risk score (GRS, also known as polygenic risk score) analysis is an increasingly popular method for exploring genetic architectures and relationships of complex diseases. However, complex diseases are usually measured by multiple correlated phenotypes. Analyzing each disease phenotype individually is likely to reduce statistical power due to multiple testing correction. In order to conquer the disadvantage, we proposed a principal component analysis (PCA)–based GRS analysis approach. Extensive simulation studies were conducted to compare the performance of PCA-based GRS analysis and traditional GRS analysis approach. Simulation results observed significantly improved performance of PCA-based GRS analysis compared to traditional GRS analysis under various scenarios. For the sake of verification, we also applied both PCA-based GRS analysis and traditional GRS analysis to a real Caucasian genome-wide association study (GWAS) data of bone geometry. Real data analysis results further confirmed the improved performance of PCA-based GRS analysis. Given that GWAS have flourished in the past decades, our approach may help researchers to explore the genetic architectures and relationships of complex diseases or traits.