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hclr.aov <- function(x, ina) {
ina <- as.numeric(ina)
g <- max(ina) ## how many groups are there
p <- dim(x)[2] ## dimensionality of the data
n <- dim(x)[1] ## sample size of the data
S <- rowsum(x, ina)
Ri <- sqrt( Rfast::rowsums(S^2) ) ## the resultant length of each group
S <- Rfast::colsums(S)
R <- sqrt( sum(S^2) ) ## the resultant length based on all the data
Apk <- function(p, k) besselI(k, p/2, expon.scaled = TRUE) / besselI(k, p/2 - 1, expon.scaled = TRUE)
## Next we estimate the common concentration parameter kappa under H0 and H1
Rk <- R/n
k1 <- Rk * (p - Rk^2)/(1 - Rk^2)
k2 <- k1 - (Apk(p, k1) - Rk) / ( 1 - Apk(p, k1)^2 - (p - 1)/k1 * Apk(p, k1) )
while ( abs(k2 - k1) > 1e-07 ) {
k1 <- k2
k2 <- k1 - (Apk(p, k1) - Rk) / (1 - Apk(p, k1)^2 - (p - 1)/k1 * Apk(p, k1) )
}
k0 <- k2 ## concentration parameter under H0
Rk <- sum(Ri)/n
k1 <- Rk * (p - Rk^2)/(1 - Rk^2)
k2 <- k1 - (Apk(p, k1) - Rk) / ( 1 - Apk(p, k1)^2 - (p - 1)/k1 * Apk(p, k1) )
while ( abs(k2 - k1) > 1e-07 ) {
k1 <- k2
k2 <- k1 - (Apk(p, k1) - Rk) / ( 1 - Apk(p, k1)^2 - (p - 1)/k1 * Apk(p, k1) )
}
k1 <- k2 ## concentration parameter under H1
I0 <- besselI( k0, p/2 - 1 )
I1 <- besselI( k1, p/2 - 1 )
Apk0 <- Apk(p, k0)
Apk1 <- Apk(p, k1)
up <- k0^(p/2 - 1) / I0 * exp(k0 * Apk0)
down <- k1^(p/2 - 1) / I1 * exp(k1 * Apk1)
P <- (n - g) / (g - 1) * ( (up / down)^( -2/(p - 1) ) - 1 )
p.value <- pf(P, (g - 1) * (p - 1), (n - g) * (p - 1), lower.tail = FALSE)
statistic <- P ; names(statistic) <- "F-test statistic"
parameter <- c( (g - 1) * (p - 1), (n - g) * (p - 1) ) ; names(parameter) <- c("df1", "df2")
alternative <- "At least one directional mean vector differs"
method <- "ANOVA for directional data using the high concentration log-likelihood ratio test"
data.name <- c("data ", " groups")
result <- list( statistic = statistic, parameter = parameter, p.value = p.value,
alternative = alternative, method = method, data.name = data.name )
class(result) <- "htest"
return(result)
}
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