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GeneticPower.Quantitative.Factor <- function(N=1000,
delta=1,
freq=0.15,
minh=c("additive","dominant","recessive"),
sigma=1,
OtherParms=0,
alpha=0.05,
numtests=1,
moi=NULL,
rsquared=NULL)
{
## N = total samples in the analysis
## delta = mean(bb) - mean (AA), where 'b' is the disease allele, 'A' is the reference allele
## freq = allele frequency of disease allele 'b'
## minh = mode of inheritance: "recessive", "additive", "dominant" same as moi=0,0.5, and 1.0, respectively
## defaults to "additive" if no moi specified eith
## sigma = standard deviation of the response phenotype
## OtherParms = the number of additional parameters (really, DOF) in the model that will reduce your overall DOF
## alpha = the desired significance level
## numtests = the number of tests to be corrected by Bonferroni adjustment beforee achieving 'alpha'
## moi = mode of inheritance: 0 for recessive, 0.5 for additive, 1.0 for dominant, or anywhere in between,
## this OVER-RIDES minh...useful for modeling i-between moi's...
## rsquared = fraction of total sum-of-squares explained by fit. OVER-RIDES delta AND sigma.
alphy <- 1-(1-alpha)^(1/numtests);
if (is.null(moi)) {
minh <- match.arg(minh) # can use abbreviated names
moi <- switch(minh,
additive = 0.5,
dominant = 1.0,
recessive = 0 ) # define the mode of inheritance
}
N1 <- N*(1-freq)^2;
N2 <- 2*N*freq*(1-freq);
N3 <- N*freq^2;
mu <- c(0,moi,1)*delta;
mu.bar <- (mu[1]*N1+mu[2]*N2+mu[3]*N3)/N;
lambda <- ifelse(is.null(rsquared),
(N1*(mu[1]-mu.bar)^2+N2*(mu[2]-mu.bar)^2+N3*(mu[3]-mu.bar)^2)/(sigma^2),
(N-3)*rsquared/(1-rsquared)
);
power <- pf(qf(1-alphy,df1=2,df2=(N-3-OtherParms)),ncp=lambda,df1=2,df2=(N-3-OtherParms),lower.tail=F)
return(power)
}
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