ade4 (version 1.7-22)

loocv.between: Leave-one-out cross-validation for a bca

Description

Leave-one-out cross-validation for bca.

Usage

# S3 method for between
loocv(x, nax = 0, progress = FALSE, parallel = FALSE, ...)
# S3 method for bcaloocv
print(x, ...)
# S3 method for bcaloocv
plot(x, xax = 1, yax = 2, ...)

Value

A list with:- XValCoord: the cross-validated row coordinates - PRESS: the Predicted Residual Error Sum for each row- PRESSTot: the sum of PRESS for each bca axis - Oij_bga: the mean overlap index for BGA- Oij_XVal: the mean overlap index for cross-validation- DeltaOij: the spuriousness index

Arguments

x

dudi of the bca on which cross-validation should be done

nax

list of axes for mean overlap index computation (0 = all axes)

progress

logical, TRUE = display a progress bar during computations

parallel

logical, TRUE = process cross-validation in parallel computing

xax, yax

the numbers of the x-axis and the y-axis

...

further arguments passed to or from other methods

Author

Jean Thioulouse

Details

This function returns a list containing the cross-validated coordinates of the rows (the rows of the original analysis, not the rows of the bca). The dudi on which the bca was computed is redone after removing each row of the data table, one at a time. A bca is done on this new dudi and the coordinates of the missing row are computed by projection as supplementary element in the corresponding bca. This is most useful in the case p >> n (many variables and few samples), where bca graphs can show spurious groups (see Refs.)

For parallel computing (parallel argument = TRUE), the new dudi, bca and cross-validation computations are processed in parallel on all the available nodes of the computer processor(s).

References

Thioulouse J, Renaud S, Dufour AB, Dray S. Overcoming the Spurious Groups Problem in Between-Group PCA. Evolutionary Biology (2021). (Accepted).

Cardini A, Polly D. Cross-validated Between Group PCA Scatterplots: A Solution to Spurious Group Separation ? Evolutionary Biology (2020) 47:85–95. tools:::Rd_expr_doi("10.1007/s11692-020-09494-x")

Cardini A, O'Higgins P, Rohlf J. Seeing Distinct Groups Where There are None: Spurious Patterns from Between-Group PCA. Evolutionary Biology (2019) 46:303-316. tools:::Rd_expr_doi("10.1007/s11692-019-09487-5")

Bookstein F. Pathologies of Between-Groups Principal Components Analysis in Geometric Morphometrics. Evolutionary Biology (2019) 46:271-302. tools:::Rd_expr_doi("10.1007/s11692-019-09484-8")

See Also

loocv.dudi loocv.discrimin

Examples

# Data = meaudret
data(meaudret)
pca1 <- dudi.pca(meaudret$env, scannf = FALSE, nf = 3)
bca1 <- bca(pca1, meaudret$design$site, scannf = FALSE, nf = 3)
pst1 <- paste0("Meaudret BGA randtest: p=",
randtest(bca1)$pvalue, " ratio=", round(bca1$ratio, 2))
xbca1 <- loocv(bca1, progress = TRUE)

if(adegraphicsLoaded()){
    sc1 <- s.class(bca1$ls, meaudret$design$site, col = TRUE,
    psub.text = pst1, ellipseSize=0, chullSize=1, plot = FALSE)
    sc2 <- s.class(xbca1$XValCoord, meaudret$design$site,
    col = TRUE, psub.text = "Meaudret cross-validation",
    ellipseSize=0, chullSize=1, plot = FALSE)
    ADEgS(list(sc1, sc2))
} else {
	par(mfrow=c(2,2))
	s.chull(dfxy = bca1$ls, fac = meaudret$design$site, cpoint = 1, 
    	col = hcl.colors(5, "Dark 2"), sub = pst1)
    s.class(bca1$ls, meaudret$design$site, col = hcl.colors(5, "Dark 2"),
    	cellipse = 0, add.plot = TRUE)
	s.chull(dfxy = xbca1$XValCoord, fac = meaudret$design$site, cpoint = 1, 
    	col = hcl.colors(5, "Dark 2"), sub = "Meaudret cross-validation")
    s.class(xbca1$XValCoord, meaudret$design$site, col = hcl.colors(5, "Dark 2"),
    	cellipse = 0, add.plot = TRUE)
}
if (FALSE) {
# Data = rnorm()
set.seed(9)
fac1 <- as.factor(rep(1:3, each = 10))
tab <- as.data.frame(matrix(rnorm(10800), nrow = 30))
pca2 <- dudi.pca(tab, scannf = FALSE)
bca2 <- bca(pca2, fac1, scannf = FALSE)
pst2 <- paste0("rnorm spurious groups: p=",
randtest(bca2)$pvalue, " ratio=", round(bca2$ratio, 2))
xbca2 <- loocv(bca2, progress = TRUE)
if(adegraphicsLoaded()){
	sc3 <- s.class(bca2$ls, fac1, col = TRUE,
		psub.text = pst2, ellipseSize=0, chullSize=1,
		xlim = c(-8, 8), ylim = c(-8, 8), plot = FALSE)
	sc4 <- s.class(xbca2$XValCoord, fac1, col = TRUE,
		psub.text = "rnorm cross-validation", ellipseSize=0,
		chullSize=1, xlim = c(-8, 8), ylim = c(-8, 8), plot = FALSE)
	ADEgS(list(sc3, sc4))
} else {
	par(mfrow=c(2,2))
	s.chull(bca2$ls, fac1, optchull = 1, cpoint = 1, xlim = c(-8, 8), ylim = c(-8, 8),
    	col = hcl.colors(3, "Dark 2"), sub = pst2)
    s.class(bca2$ls, fac1, xlim = c(-8, 8), ylim = c(-8, 8),
    	col = hcl.colors(3, "Dark 2"), cellipse = 0, add.plot = TRUE)
	s.chull(xbca2$XValCoord, fac1, optchull = 1, cpoint = 1, xlim = c(-8, 8),
		ylim = c(-8, 8), col = hcl.colors(3, "Dark 2"), sub = "rnorm cross-validation")
    s.class(xbca2$XValCoord, fac1, xlim = c(-8, 8), ylim = c(-8, 8),
    	col = hcl.colors(3, "Dark 2"), cellipse = 0, add.plot = TRUE)
}
}