User:Timothee Flutre/Notebook/Postdoc/2011/06/28
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Linear regression by ordinary least squares
In vector-matrix notation:
The parameters of the model are: Θ = {μ,β,σ}
The well-known ordinary-least-square (OLS) estimator of B is:
Let's now define 4 summary statistics, very easy to compute:
This allows to obtain the estimate of the effect size only by having the summary statistics available:
By the way, in this case (i.e. simple linear regression, a single predictor), it's easy to see that:
The same works for the estimate of the standard deviation of the errors:
We can also benefit from this for the standard error of the parameters:
which corresponds to:
V(y) = V(μ + βg + ε) = V(μ) + V(βg) + V(ε) = β2V(g) + σ2 The most intuitive way to simulate data is therefore to fix the proportion of variance in y explained by the genotype, for instance PVE = 60%, as well as the standard deviation of the errors, typically σ = 1. From this, we can calculate the corresponding effect size β of the genotype:
Therefore:
Note that g is the random variable corresponding to the genotype encoded in allele dose, such that it is equal to 0, 1 or 2 copies of the minor allele. For our simulation, we will fix the minor allele frequency f (eg. f = 0.3) and we will assume Hardy-Weinberg equilibrium. Then g is distributed according to a binomial distribution with 2 trials for which the probability of success is f. As a consequence, its variance is V(g) = 2f(1 − f). Here is some R code implementing all this:
set.seed(1859)
N <- 100 # sample size
mu <- 4
pve <- 0.6
sigma <- 1
maf <- 0.3 # minor allele frequency
beta <- sigma * sqrt(pve / ((1 - pve) * 2 * maf * (1 - maf))) # 1.89
g <- rbinom(n=N, size=2, prob=maf) # assuming Hardy-Weinberg equilibrium
y <- mu + beta * g + rnorm(n=N, mean=0, sd=sigma)
ols <- lm(y ~ g)
summary(ols) # muhat=4.1+-0.13, betahat=1.6+-0.16, R2=0.49
sqrt((1/(N-2) * sum(ols$residuals^2))) # sigmahat=0.99
plot(x=0, type="n", xlim=range(g), ylim=range(y),
xlab="genotypes (allele counts)", ylab="phenotypes",
main="Simple linear regression")
for(i in unique(g))
points(x=jitter(g[g == i]), y=y[g == i], col=i+1, pch=19)
abline(a=coefficients(ols)[1], b=coefficients(ols)[2])
As above, we want X = UDVT This allows us to get the Moore-Penrose pseudoinverse matrix of X: X + = (XTX) − 1XT = VD − 1UT From this, we get the OLS estimate of the effect sizes:
Then it's straightforward to get the residuals:
With them we can calculate the estimate of the error variance:
And finally the standard errors of the estimates of the effect sizes:
We can check this with some R code: ## simulate the data set.seed(1859) N <- 100 mu <- 4 pve.g <- 0.4 # genotype pve.c <- 0.2 # other covariate, eg. gender sigma <- 1 maf <- 0.3 sex.ratio <- 0.5 beta.g <- sigma * sqrt((1 / (2 * maf * (1 - maf))) * (pve.g / (1 - pve.g - pve.c))) # 1.543 beta.c <- beta.g * sqrt((pve.c / pve.g) * (2 * maf * (1 - maf) / sex.ratio * (1 - sex.ratio))) # 0.707 x.g <- rbinom(n=N, size=2, prob=maf) x.c <- rbinom(n=N, size=1, prob=sex.ratio) y <- mu + beta.g * x.g + beta.c * x.c + rnorm(n=N, mean=0, sd=sigma) ols <- lm(y ~ x.g + x.c) summary(ols) # muhat=3.9+-0.17, beta.g.hat=1.6+-0.17, beta.c.hat=0.58+-0.21, R2=0.51 sqrt((1/(N-3)) * sum(ols$residuals^2)) # sigma.hat = 1.058 ## perform the OLS analysis with the SVD of X X <- cbind(rep(1,N), x.g, x.c) Xp <- svd(x=X) B.hat <- Xp$v %*% diag(1/Xp$d) %*% t(Xp$u) %*% y E.hat <- y - X %*% B.hat sigma.hat <- as.numeric(sqrt((1/(N-3)) * t(E.hat) %*% E.hat)) # 1.058 var.theta.hat <- sigma.hat^2 * Xp$v %*% diag((1/Xp$d)^2) %*% t(Xp$v) sqrt(diag(var.theta.hat)) # 0.168 0.175 0.212 Such an analysis can also be done easily in a custom C/C++ program thanks to the GSL (here). | |
the (quantitative) phenotypes (e.g. expression level at a given gene), and
the genotypes at a given SNP. We want to assess their linear relationship.
with
and
,
and
(its standard error). In the case where we don't have access to the original data (e.g. because genotypes are confidential) but only to some summary statistics (see below), it is still possible to calculate the estimates.
an Nx1 vector, X an Nx3 matrix with 1's in the first column, the genotypes in the second and the genders in the third, B a 3x1 vector and
an Nx1 vector following a multivariate Normal distribution centered on 0 and with covariance matrix
,
. To efficiently get them, we start with the


