We will start by loading the codalm R package.
We will now access the data from the ggtern package. We will be
analyzing how two different methods (image analysis or microscopic
inspection) estimate the composition of 30 white blood cells. The format
that we need is for both compositions to be in matrices, with one row
per observation. We will also normalize the rows of these matrices to
ensure that they sum to 1, although the codalm function
would also take care of this for us.
data("WhiteCells", package = 'ggtern')
image <- subset(WhiteCells, Experiment == "ImageAnalysis")
image_mat <- as.matrix(image[,c("G", "L", "M")])
microscopic <- subset(WhiteCells, Experiment == "MicroscopicInspection")
microscopic_mat <- as.matrix(microscopic[,c("G", "L", "M")])
image_mat <- image_mat / rowSums(image_mat)
microscopic_mat <- microscopic_mat / rowSums(microscopic_mat)To estimate the coefficient matrix B, we can use the
codalm function.
B_est <- codalm(y = microscopic_mat, x = image_mat)
B_est
#> [,1] [,2] [,3]
#> [1,] 9.742582e-01 0.02292755 2.814241e-03
#> [2,] 3.267625e-09 1.00000000 3.620985e-10
#> [3,] 9.484170e-18 0.04198815 9.580118e-01To see the interpretation of this matrix, please see Fiksel et al. (2022). If
all the rows of B_est are exactly the same, it is recommended to set
accelerate = FALSE as a sensitivity check.
We can also use the bootstrap to estimate 95% confidence intervals. We will only use 50 bootstrap iterations as an example (nboot = 50), but is recommended to do more.
B_ci <- codalm_ci(y = microscopic_mat, x = image_mat, nboot = 50,
conf = .95)
#> Warning: package 'future' was built under R version 4.5.2
B_ci$ci_L
#> [,1] [,2] [,3]
#> [1,] 9.576089e-01 0.01399186 1.156448e-03
#> [2,] 2.512037e-15 0.97220006 9.834101e-17
#> [3,] 1.343387e-20 0.01165546 9.145955e-01
B_ci$ci_U
#> [,1] [,2] [,3]
#> [1,] 9.837854e-01 0.03981767 4.560504e-03
#> [2,] 2.779953e-02 1.00000000 4.227865e-07
#> [3,] 3.143547e-06 0.08540455 9.868145e-01These matrices given the lower and upper bounds for the confidence interval for each element of the coefficient matrix.
You can also take advantage of parallelization, if you have multiple cores available.
ncores <- 2
Sys.setenv(R_FUTURE_SUPPORTSMULTICORE_UNSTABLE = "quiet")
B_ci_parallel <- codalm_ci(y = microscopic_mat, x = image_mat, nboot = 50,
conf = .95, parallel = TRUE, ncpus = ncores, strategy = 'multisession')
#> Warning: package ‘future’ was built under R version 4.5.2
#> Warning: package ‘future’ was built under R version 4.5.2
isTRUE(all.equal(B_ci$ci_L, B_ci_parallel$ci_L))
#> [1] TRUE
isTRUE(all.equal(B_ci$ci_U, B_ci_parallel$ci_U))
#> [1] TRUE
# identical(B_ci$ci_L, B_ci_parallel$ci_L)
# identical(B_ci$ci_U, B_ci_parallel$ci_U)Finally, we will do a permutation test for linear independence. Again, we will only do 50 permutations as an example, but in practice this number should be higher. For demonstration purposes, we will generate the compositional outcome independently of the compositional predictor
set.seed(123)
x <- gtools::rdirichlet(100, rep(1, 3))
y <- gtools::rdirichlet(100, rep(1, 3))
indep_test_pval <- codalm_indep_test(y = y, x = x,
nperms = 100, init.seed = 123)
indep_test_pval
#> [1] 0.28This function can also be parallelized. Unlike the bootstrapping, there is no need to differentiate between whether the user is using a Windows or Unix system.
indep_test_pval_parallel <- codalm_indep_test(y = y, x = x,
nperms = 100, init.seed = 123,
parallel = TRUE, ncpus = ncores,
strategy = 'multisession')
#> Warning: package ‘future’ was built under R version 4.5.2
#> Warning: package ‘future’ was built under R version 4.5.2
indep_test_pval_parallel
#> [1] 0.28