TY - JOUR
T1 - A penalized regression approach for integrative analysis in gen ome- wide association studies
AU - Liu, J.
AU - Wang, F.
AU - Gao, X.
AU - Zhang, H.
AU - Wan, Xiang
AU - Yang, Can
N1 - This study was supported by National Institutes of Health grants R01EY022651, Hong Kong Research grant HKBU12202114, Hong Kong Baptist University FRG2/13-14/005 and Duke- NUS Graduate Medical School WBS: R-913-200-098-263.
PY - 2015/5
Y1 - 2015/5
N2 - Over one thousand genome-wide association studies (GWAS) have been conducted in the past decade. Increasing biological evidence suggests the polygenic genetic architecture of complex traits: a complex trait is affected by many risk variants with small or moderate effects jointly. Meanwhile, recent progress in GWAS suggests that complex human traits may share common genetic bases, which is known as “pleiotropy”. To further improve statistical power of detecting risk genetic variants in GWAS, we propose a penalized regression method to analyze the GWAS dataset of primary interest by incorporating information from other related GWAS. The proposed method does not require the individual-level of genotype and phenotype data from other related GWAS, making it useful when only summary statistics are available. The key idea of the proposed approach is that related traits may share common genetic basis. Specifically, we propose a linear model for integrative analysis of multiple GWAS, in which risk genetic variants can be detected via identification of nonzero coefficients. Due to the pleiotropy effect, there exist genetic variants affecting multiple traits, which correspond to a consistent nonzero pattern of coefficients across multiple GWAS. To achieve this, we use a group Lasso penalty to identify this nonzero pattern in our model, and then develop an efficient algorithm based on the proximal gradient method. Simulation studies showed that the proposed approach had satisfactory performance. We applied the proposed method to analyze a body mass index (BMI) GWAS dataset from a European American (EA) population and achieved improvement over single GWAS analysis.
AB - Over one thousand genome-wide association studies (GWAS) have been conducted in the past decade. Increasing biological evidence suggests the polygenic genetic architecture of complex traits: a complex trait is affected by many risk variants with small or moderate effects jointly. Meanwhile, recent progress in GWAS suggests that complex human traits may share common genetic bases, which is known as “pleiotropy”. To further improve statistical power of detecting risk genetic variants in GWAS, we propose a penalized regression method to analyze the GWAS dataset of primary interest by incorporating information from other related GWAS. The proposed method does not require the individual-level of genotype and phenotype data from other related GWAS, making it useful when only summary statistics are available. The key idea of the proposed approach is that related traits may share common genetic basis. Specifically, we propose a linear model for integrative analysis of multiple GWAS, in which risk genetic variants can be detected via identification of nonzero coefficients. Due to the pleiotropy effect, there exist genetic variants affecting multiple traits, which correspond to a consistent nonzero pattern of coefficients across multiple GWAS. To achieve this, we use a group Lasso penalty to identify this nonzero pattern in our model, and then develop an efficient algorithm based on the proximal gradient method. Simulation studies showed that the proposed approach had satisfactory performance. We applied the proposed method to analyze a body mass index (BMI) GWAS dataset from a European American (EA) population and achieved improvement over single GWAS analysis.
KW - Integrative analysis of GWAS
KW - Penalized methods
KW - Scaled group Lasso
U2 - 10.4172/2155-6180.1000228
DO - 10.4172/2155-6180.1000228
M3 - Journal article
SN - 2155-6180
VL - 6
JO - Journal of Biometrics and Biostatistics
JF - Journal of Biometrics and Biostatistics
IS - 2
M1 - 28286
ER -