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Ballard, J. L.

Publications and source records attributed to Ballard, J. L..

2 recordsLinked to original sources

Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies

Linkage disequilibrium (LD) is the correlation among nearby genetic variants. In genetic association studies, LD is often modeled using massive local correlation matrices, but this approach is slow, especially in ancestrally diverse studies. Here, we introduce LD graphical models (LDGMs), which are an extremely sparse and efficient representation of LD. LDGMs are derived from genome-wide genealogies; statistical relationships among alleles in the LDGM correspond to genealogical relationships among haplotypes. We publish LDGMs and ancestry specific LDGM precision matrices for 18 million common SNPs (MAF>1%) in five ancestry groups, validate their accuracy, and demonstrate order-of-magnitude improvements in runtime for commonly used LD matrix computations. We implement an extremely fast multi-ancestry polygenic prediction method, BLUPx-ldgm, which performs better than a similar method based on the reference LD correlation matrix. LDGMs will enable sophisticated methods that scale to ancestrally genetic association data across millions of variants and individuals.

genetics↗

Shared components of heritability across genetically correlated traits

Most disease-associated genetic variants are pleiotropic, affecting multiple genetically correlated traits. Their pleiotropic associations can be mechanistically informative: if many variants have similar patterns of association, they may act via similar pleiotropic mechanisms, forming a shared component of heritability. We developed Pleiotropic Decomposition Regression (PDR) to identify shared components and their underlying genetic variants. We validated PDR on simulated data and identified limitations of existing methods in recovering the true components. We applied PDR to three clusters of 5-6 traits genetically correlated with coronary disease, asthma, and type II diabetes respectively, producing biologically interpretable components. For CAD, PDR identified components related to BMI, hypertension and cholesterol, and it clarified the relationship among these highly correlated risk factors. We assigned variants to components, calculated their posterior-mean effect sizes, and performed out-of-sample validation. Our posterior-mean effect sizes pool statistical power across traits and substantially boost the correlation (r2) between true and estimated effect sizes compared with the original summary statistics: by 94% and 70% for asthma and T2D out of sample, and by a predicted 300% for CAD.

genetics↗