--- title: "A set-based association test in snpsettest" author: "Jaehyun Joo" date: "`r format(Sys.time(), '%d %B, %Y')`" output: rmarkdown::html_vignette vignette: > %\VignetteIndexEntry{A set-based association test in snpsettest} %\VignetteEngine{knitr::rmarkdown} %\VignetteEncoding{UTF-8} --- For set-based association tests, the **snpsettest** package employed the statistical model described in VEGAS (**ve**rsatile **g**ene-based **a**ssociation **s**tudy) [1], which takes as input variant-level p values and reference linkage disequilibrium (LD) data. Briefly, the test statistics is defined as the sum of squared variant-level Z-statistics. Letting a set of $Z$ scores of individual SNPs $z_i$ for $i \in 1:p$ within a set $s$, the test statistic $Q_s$ is $$Q_s = \sum_{i=1}^p z_i^2$$ Here, $Z = \{z_1,...,z_p\}'$ is a vector of multivariate normal distribution with a mean vector $\mu$ and a covariance matrix $\Sigma$ in which $\Sigma$ represents LD among SNPs. To test a set-level association, we need to evaluate the distribution of $Q_s$. VEGAS uses Monte Carlo simulations to approximate the distribution of $Q_s$ (directly simulate $Z$ from multivariate normal distribution), and thus, compute a set-level p value. However, its use is hampered in practice when set-based p values are very small because the number of simulations required to obtain such p values is be very large. The **snpsettest** package utilizes a different approach to evaluate the distribution of $Q_s$ more efficiently. Let $Y = \Sigma^{-\frac12}Z$ (instead of $\Sigma^{-\frac12}$, we could use any decomposition that satisfies $\Sigma = AA'$ with a $p \times p$ non-singular matrix $A$ such that $Y = A^{-1}Z$). Then, $$ \begin{gathered} E(Y) = \Sigma^{-\frac12} \mu \\ Var(Y) = \Sigma^{-\frac12}\Sigma\Sigma^{-\frac12} = I_p \\ Y \sim N(\Sigma^{-\frac12} \mu,~I_p) \end{gathered} $$ Now, we posit $U = \Sigma^{-\frac12}(Z - \mu)$ so that $$U \sim N(\mathbf{0}, I_p),~~U = Y - \Sigma^{-\frac12}\mu$$ and express the test statistic $Q_s$ as a quadratic form: $$ \begin{aligned} Q_s &= \sum_{i=1}^p z_i^2 = Z'I_pZ = Y'\Sigma^{\frac12}I_p\Sigma^{\frac12}Y \\ &= (U + \Sigma^{-\frac12}\mu)'\Sigma(U + \Sigma^{-\frac12}\mu) \end{aligned} $$ With the spectral theorem, $\Sigma$ can be decomposed as follow: $$ \begin{gathered} \Sigma = P\Lambda P' \\ \Lambda = \mathbf{diag}(\lambda_1,...,\lambda_p),~~P'P = PP' = I_p \end{gathered} $$ where $P$ is an orthogonal matrix. If we set $X = P'U$, $X$ is a vector of independent standard normal variable $X \sim N(\mathbf{0}, I_p)$ since $$E(X) = P'E(U) = \mathbf{0},~~Var(X) = P'Var(U)P = P'I_pP = I_p$$ $$ \begin{aligned} Q_s &= (U + \Sigma^{-\frac12}\mu)'\Sigma(U + \Sigma^{-\frac12}\mu) \\ &= (U + \Sigma^{-\frac12}\mu)'P\Lambda P'(U + \Sigma^{-\frac12}\mu) \\ &= (X + P'\Sigma^{-\frac12}\mu)'\Lambda (X + P'\Sigma^{-\frac12}\mu) \end{aligned} $$ Under the null hypothesis, $\mu$ is assumed to be $\mathbf{0}$. Hence, $$Q_s = X'\Lambda X = \sum_{i=1}^p \lambda_i x_i^2$$ where $X = \{x_1,...,x_p\}'$. Thus, the null distribution of $Q_s$ is a linear combination of independent chi-square variables $x_i^2 \sim \chi_{(1)}^2$ (i.e., central quadratic form in independent normal variables). For computing a probability with a scalar $q$, $$Pr(Q_s > q)$$ several methods have been proposed, such as numerical inversion of the characteristic function [2]. The **snpsettest** package uses the algorithm of Davies [3] or saddlepoint approximation [4] to obtain set-based p values. **References** 1. Liu JZ, Mcrae AF, Nyholt DR, Medland SE, Wray NR, Brown KM, et al. A Versatile Gene-Based Test for Genome-wide Association Studies. Am J Hum Genet. 2010 Jul 9;87(1):139–45. 2. Duchesne P, De Micheaux P. Computing the distribution of quadratic forms: Further comparisons between the Liu-Tang-Zhang approximation and exact methods. Comput Stat Data Anal. 2010;54:858–62. 3. Davies RB. Algorithm AS 155: The Distribution of a Linear Combination of Chi-square Random Variables. J R Stat Soc Ser C Appl Stat. 1980;29(3):323–33. 4. Kuonen D. Saddlepoint Approximations for Distributions of Quadratic Forms in Normal Variables. Biometrika. 1999;86(4):929–35.