knitr::opts_chunk$set( collapse = TRUE, comment = "#>" ) knitr::opts_chunk$set(warning = FALSE, message=FALSE, error=TRUE, purl=FALSE)
library(discnorm ) library(lavaan)
The discnorm package uses bootstrapping to help determine whether the commonly assumed normality assumption is tenable for an ordinal dataset. Researchers wanting to proceed with ordinal SEM based on polychoric correlations should first to check that the normalit copula assumption is not violated. Also, if the normality assumption is tenable, researchers may specify other marginal distributions using catLSadjust().
The procedure is named bootTest() and operates on an ordinal dataset and returns a p-value associated with the null-hypothesis of underlying normality. Let us first use the test for a dataset that is produced by underlying normality.
#let us discretize an underlying normal vector # with moderate correlation rho <- 0.3 Sigma <- diag(5) Sigma[Sigma !=1] <- rho set.seed(1234) norm.sample <- MASS::mvrnorm(n=200, mu=rep(0,5), Sigma=Sigma) # let us discretize into 4 categories disc.sample <- apply(norm.sample, 2, cut, breaks=c(-Inf, -1, 1, 2, Inf), labels=FALSE) #check for underlying normality pvalue <- bootTest(disc.sample, B=500) print(pvalue) # we have no evidence against the null hypothesis of underlying normality
And let us discretize a non-normal dataset
nonnorm.sample <- data.frame(norm.sample[, 1:4], norm.sample[,1]*norm.sample[,2]) disc.sample2 <- apply(nonnorm.sample, 2, cut, breaks=c(-Inf, -1, 1, 2, Inf), labels=FALSE) pvalue <- bootTest(disc.sample2, B=500) print(pvalue) # rejected!
The procedure is fully described in @fold1
First we generate a large dataset with non-normal marginals by transforming the marginals of a normal dataset
shape= 2 scale = 1/sqrt(shape) m1 <- list(F=function(x) pchisq(x, df=1), qF=function(x) qchisq(x, df=1), sd=sqrt(2)) G3 <- function(x) pgamma(x+shape*scale, shape=shape, scale=scale) G3flip <- function(x) 1- G3(-x) qG3 <- function(x) qgamma(x, shape=shape, scale=scale)-shape*scale qG3flip <- function(x) -qG3(1-x) marginslist <- list(m1, list(F=G3, qF=qG3), list(F=G3flip, qF=qG3flip)) Sigma <- diag(3) Sigma[Sigma==0] <- 0.5 Sigma set.seed(1) norm.data <- MASS::mvrnorm(10^5, rep(0,3), Sigma) colnames(norm.data) <- c("x1", "x2", "x3") #With normal marginals, the correlation matrix is (approximately) #Sigma. #Transform the marginals to follow the elements in marginslist: nonnorm.data <- data.frame(x1=marginslist[[1]]$qF(pnorm(norm.data[, 1])), x2=marginslist[[2]]$qF(pnorm(norm.data[, 2])), x3=marginslist[[3]]$qF(pnorm(norm.data[, 3]))) cor(nonnorm.data)
Next we fit both the normal and the non-normal datasets to a factor model (which fits perfectly to both sets), and look at factor loading parameters
head(standardizedsolution(cfa("F=~ x1+x2+x3", norm.data)),3) head(standardizedsolution(cfa("F=~ x1+x2+x3", nonnorm.data)),3)
Then we discretize the non-normal dataset and confirm that the strongly polychoric correlations are strongly biased
disc.data <- data.frame(x1=cut(nonnorm.data[, 1], breaks= c(-Inf, 0.1, 1, Inf), labels=FALSE), x2= cut(nonnorm.data[, 2], breaks= c(-Inf, -.7, 0,1, Inf), labels=FALSE), x3=cut(nonnorm.data[, 3], breaks= c(-Inf, -1, 0,1, Inf), labels=FALSE)) lavaan::lavCor(disc.data, ordered=colnames(disc.data))
Next, compute the adjusted correlations and the associated standard error. Confirm that the correlations are close to those in the original non-normal dataset:
adjusted <- catLSadj(disc.data, marginslist, verbose=T ) adjusted[[1]]
Running conventional ordinal factor analysis leads to biased factor loadings:
head(standardizedsolution(fcat <- cfa("F=~ x1+x2+x3", disc.data, ordered=colnames(disc.data))),3)
These parameter estimates are close to the parameters of the continuous model for normal data, and not to the model parameters obtained from the discretized non-normal dataset To get consistent estimates of these parameters we need to use the adjusted polychoric correlation.
sample.th <- lavInspect(fcat, "sampstat")$th attr(sample.th, "th.idx") <- lavInspect(fcat, "th.idx") #the asymptotic covariance matrix of the adjusted polychorics: gamma.adj <- adjusted[[2]] WLS.V.new <- diag(1/diag(gamma.adj)) fcat.adj <- cfa("F=~ x1+x2+x3", sample.cov=adjusted[[1]], sample.nobs=nrow(disc.data), sample.th=sample.th, NACOV = gamma.adj, WLS.V=WLS.V.new) head(standardizedsolution(fcat.adj), 3)
Closely matches the model parameters obtained with the non-normal dataset
The procedure is fully described in @fold2
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