A distance measure closely related to the Hellinger distance.
Usage
matusita(counts, margin = 1L, pairs = NULL, cpus = n_cpus())Arguments
- counts
A numeric matrix of count data (samples \(\times\) features). Typically contains absolute abundances (integer counts), though proportions are also accepted.
- margin
The margin containing samples.
1if samples are rows,2if samples are columns. Ignored whencountsis a special object class (e.g.phyloseq). Default:1- pairs
Which combinations of samples should distances be calculated for? The default value (
NULL) calculates all-vs-all. Provide a numeric or logical vector specifying positions in the distance matrix to calculate. See examples.- cpus
How many parallel processing threads should be used. The default,
n_cpus(), will use all logical CPU cores.
Details
The Matusita distance is defined as: $$\sqrt{\sum_{i=1}^{n}\left(\sqrt{P_i} - \sqrt{Q_i}\right)^2}$$
Where:
\(P_i\), \(Q_i\) : Proportional abundances of the \(i\)-th feature.
\(n\) : The number of features.
Base R Equivalent:
Input Types
The counts parameter is designed to accept a simple numeric matrix, but
seamlessly supports objects from the following biological data packages:
phyloseqrbiomSummarizedExperimentTreeSummarizedExperiment
For large datasets, standard matrix operations may be slow. See
vignette('performance') for details on using optimized formats
(e.g. sparse matrices) and parallel processing.
References
Matusita, K. (1955). Decision rules, based on the distance, for problems of fit, two samples, and estimation. The Annals of Mathematical Statistics, 26(4), 631-640. doi:10.1214/aoms/1177728422
See also
beta_div(), vignette('bdiv'), vignette('bdiv_guide')
Other Abundance metrics:
aitchison(),
bhattacharyya(),
bray(),
canberra(),
chebyshev(),
chord(),
clark(),
divergence(),
euclidean(),
gower(),
hellinger(),
horn(),
jensen(),
jsd(),
lorentzian(),
manhattan(),
minkowski(),
morisita(),
motyka(),
psym_chisq(),
soergel(),
squared_chisq(),
squared_chord(),
squared_euclidean(),
topsoe(),
wave_hedges()
