library(phylobase)
This document describes the new 'phylo4' S4 classes and methods, which
are intended to provide a unifying standard for the representation of
phylogenetic trees and comparative data in R. The phylobase
package
was developed to help both end users and package developers by providing
a common suite of tools likely to be shared by all packages designed for
phylogenetic analysis, facilities for data and tree manipulation, and
standardization of formats.
This standardization will benefit end-users by making it easier to
move data and compare analyses across packages, and to keep comparative
data synchronized with phylogenetic trees. Users will also benefit from
a repository of functions for tree manipulation, for example tools for
including or excluding subtrees (and associated phenotypic data) or
improved tree and data plotting facilities. phylobase
will benefit
developers by freeing them to put their programming effort into
developing new methods rather than into re-coding base tools. We (the
phylobase
developers) hope phylobase
will also facilitate code
validation by providing a repository for benchmark tests, and more
generally that it will help catalyze community development of
comparative methods in R.
A more abstract motivation for developing phylobase
was to improve
data checking and abstraction of the tree data formats. phylobase
can
check that data and trees are associated in the proper fashion, and
protects users and developers from accidently reordering one, but not
the other. It also seeks to abstract the data format so that commonly
used information (for example, branch length information or the ancestor
of a particular node) can be accessed without knowledge of the
underlying data structure (i.e., whether the tree is stored as a matrix,
or a list, or a parenthesis-based format). This is achieved through
generic phylobase
functions which which retrieve the relevant
information from the data structures. The benefits of such abstraction
are multiple: (1) easier access to the relevant information via a
simple function call (this frees both users and developers from learning
details of complex data structures), (2) freedom to optimize data
structures in the future without breaking code. Having the generic
functions in place to "translate" between the data structures and the
rest of the program code allows program and data structure development
to proceed somewhat independently. The alternative is code written for
specific data structures, in which modifications to the data structure
requires rewriting the entire package code (often exacting too high a
price, which results in the persistence of less-optimal data
structures). (3) providing broader access to the range of tools in
phylobase
. Developers of specific packages can use these new tools
based on S4 objects without knowing the details of S4 programming.
The base 'phylo4' class is modeled on the the phylo
class in ape
.
and extend the 'phylo4' class to include data or multiple trees
respectively. In addition to describing the classes and methods, this
vignette gives examples of how they might be used.
The phylobase package currently implements the following functions and data structures:
Data structures for storing a single tree and multiple trees: and ?
A data structure for storing a tree with associated tip and node data:
A data structure for storing multiple trees with one set of tip data:
Functions for reading nexus files into the above data structures
Functions for converting between the above data structures and
objects as well as phylog
objects (although the latter are now
deprecated ...)
Functions for editing trees and data (i.e., subsetting and replacing)
Functions for plotting trees and trees with data
The help system works similarly to the help system with some small
differences relating to how methods are written. The function is a good
example. When we type we are provided the help for the default plotting
function which expects x
and y
. R
also provides a way to smartly
dispatch the right type of plotting function. In the case of an object
(a class object) R
evaluates the class of the object and finds the
correct functions, so the following works correctly.
library(ape) set.seed(1) ## set random-number seed rand_tree <- rcoal(10) ## Make a random tree with 10 tips plot(rand_tree)
However, typing still takes us to the default plot
help. We have to
type to find what we are looking for. This is because generics are
simply functions with a dot and the class name added.
The generic system is too complicated to describe here, but doesn't
include the same dot notation. As a result doesn't work, R
still finds
the right plotting function.
library(phylobase) # convert rand_tree to a phylo4 object rand_p4_tree <- as(rand_tree, "phylo4") plot(rand_p4_tree)
All fine and good, but how to we find out about all the great features
of the phylobase
plotting function? R
has two nifty ways to find it,
the first is to simply put a question mark in front of the whole call:
`?`(plot(rand_p4_tree))
R
looks at the class of the object and takes us to the correct help
file (note: this only works with objects). The second ways is handy if
you already know the class of your object, or want to compare to
generics for different classes:
`?`(method, plot("phylo4"))
More information about how documentation works can be found in the methods package, by running the following command.
help('Documentation', package="methods")
You can start with a tree --- an object of class phylo
from the ape
package (e.g., read in using the read.tree()
or read.nexus()
functions), and convert it to a phylo4
object.
For example, load the raw Geospiza data:
library(phylobase) data(geospiza_raw) # what does it contain? names(geospiza_raw) #> [1] "tree" "data"
Convert the S3
tree to a S4 phylo4
object using the as()
function:
(g1 <- as(geospiza_raw$tree, "phylo4")) #> label node ancestor edge.length node.type #> 1 fuliginosa 1 24 0.05500 tip #> 2 fortis 2 24 0.05500 tip #> 3 magnirostris 3 23 0.11000 tip #> 4 conirostris 4 22 0.18333 tip #> 5 scandens 5 21 0.19250 tip #> 6 difficilis 6 20 0.22800 tip #> 7 pallida 7 25 0.08667 tip #> 8 parvulus 8 27 0.02000 tip #> 9 psittacula 9 27 0.02000 tip #> 10 pauper 10 26 0.03500 tip #> 11 Platyspiza 11 18 0.46550 tip #> 12 fusca 12 17 0.53409 tip #> 13 Pinaroloxias 13 16 0.58333 tip #> 14 olivacea 14 15 0.88077 tip #> 15 <NA> 15 0 NA root #> 16 <NA> 16 15 0.29744 internal #> 17 <NA> 17 16 0.04924 internal #> 18 <NA> 18 17 0.06859 internal #> 19 <NA> 19 18 0.13404 internal #> 20 <NA> 20 19 0.10346 internal #> [ reached 'max' / getOption("max.print") -- omitted 7 rows ]
The (internal) nodes appear with labels \verb+
nodeLabels(g1) #> 15 16 17 18 19 20 21 22 23 24 25 26 27 #> NA NA NA NA NA NA NA NA NA NA NA NA NA
You can also retrieve the node labels with \texttt{labels(g1,"internal")}.
A simple way to assign the node numbers as labels (useful for various checks) is
nodeLabels(g1) <- paste("N", nodeId(g1, "internal"), sep="") head(g1, 5) #> label node ancestor edge.length node.type #> 1 fuliginosa 1 24 0.05500 tip #> 2 fortis 2 24 0.05500 tip #> 3 magnirostris 3 23 0.11000 tip #> 4 conirostris 4 22 0.18333 tip #> 5 scandens 5 21 0.19250 tip
The \texttt{summary} method gives a little extra information, including information on the distribution of branch lengths:
summary(g1) #> #> Phylogenetic tree : g1 #> #> Number of tips : 14 #> Number of nodes : 13 #> Branch lengths: #> mean : 0.1764008 #> variance : 0.04624379 #> distribution : #> Min. 1st Qu. Median Mean 3rd Qu. Max. #> 0.00917 0.04985 0.08000 0.17640 0.21912 0.88077
Print tip labels:
tipLabels(g1) #> 1 2 3 4 5 6 #> "fuliginosa" "fortis" "magnirostris" "conirostris" "scandens" "difficilis" #> 7 8 9 10 11 12 #> "pallida" "parvulus" "psittacula" "pauper" "Platyspiza" "fusca" #> 13 14 #> "Pinaroloxias" "olivacea"
(labels(g1,"tip")
would also work.)
You can modify labels and other aspects of the tree --- for example, to convert all the labels to lower case:
tipLabels(g1) <- tolower(tipLabels(g1))
You could also modify selected labels, e.g. to modify the labels in positions 11 and 13 (which happen to be the only labels with uppercase letters):
tipLabels(g1)[c(11, 13)] <- c("platyspiza", "pinaroloxias")
Note that for a given tree, phylobase
always return the tipLabels
in the same order.
Print node numbers (in edge matrix order):
nodeId(g1, type='all') #> [1] 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27
Does it have information on branch lengths?
hasEdgeLength(g1) #> [1] TRUE
It does! What do they look like?
edgeLength(g1) #> 15-16 16-17 17-18 18-19 19-20 20-21 21-22 22-23 23-24 24-1 24-2 #> 0.29744 0.04924 0.06859 0.13404 0.10346 0.03550 0.00917 0.07333 0.05500 0.05500 0.05500 #> 23-3 22-4 21-5 0-15 20-6 19-25 25-7 25-26 26-27 27-8 27-9 #> 0.11000 0.18333 0.19250 NA 0.22800 0.24479 0.08667 0.05167 0.01500 0.02000 0.02000 #> 26-10 18-11 17-12 16-13 15-14 #> 0.03500 0.46550 0.53409 0.58333 0.88077
Note that the root has <NA>
as its length.
Print edge labels (also empty in this case --- therefore all NA
):
edgeLabels(g1) #> 15-16 16-17 17-18 18-19 19-20 20-21 21-22 22-23 23-24 24-1 24-2 23-3 22-4 21-5 0-15 #> NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA #> 20-6 19-25 25-7 25-26 26-27 27-8 27-9 26-10 18-11 17-12 16-13 15-14 #> NA NA NA NA NA NA NA NA NA NA NA NA
You can also use this function to label specific edges:
edgeLabels(g1)["23-24"] <- "an edge" edgeLabels(g1) #> 15-16 16-17 17-18 18-19 19-20 20-21 21-22 22-23 23-24 #> NA NA NA NA NA NA NA NA "an edge" #> 24-1 24-2 23-3 22-4 21-5 0-15 20-6 19-25 25-7 #> NA NA NA NA NA NA NA NA NA #> 25-26 26-27 27-8 27-9 26-10 18-11 17-12 16-13 15-14 #> NA NA NA NA NA NA NA NA NA
The edge labels are named according to the nodes they connect (ancestor-descendant). You can get the edge(s) associated with a particular node:
getEdge(g1, 24) # default uses descendant node #> 24 #> "23-24" getEdge(g1, 24, type="ancestor") # edges using ancestor node #> 24 24 #> "24-1" "24-2"
These results can in turn be passed to the function \texttt{edgeLength} to retrieve the length of a given set of edges:
edgeLength(g1)[getEdge(g1, 24)] #> 23-24 #> 0.055 edgeLength(g1)[getEdge(g1, 24, "ancestor")] #> 24-1 24-2 #> 0.055 0.055
Is it rooted?
isRooted(g1) #> [1] TRUE
Which node is the root?
rootNode(g1) #> N15 #> 15
Does it contain any polytomies?
hasPoly(g1) #> [1] FALSE
Is the tree ultrametric?
isUltrametric(g1) #> [1] TRUE
You can also get the depth (distance from the root) of any given node or the tips:
nodeDepth(g1, 23) #> Warning: 'nodeDepth' is deprecated. #> Use 'nodeHeight' instead. #> See help("Deprecated") #> N23 #> 0.77077 depthTips(g1) #> Warning: 'depthTips' is deprecated. #> Use 'nodeHeight' instead. #> See help("Deprecated") #> Warning: 'nodeDepth' is deprecated. #> Use 'nodeHeight' instead. #> See help("Deprecated") #> fuliginosa fortis magnirostris conirostris scandens difficilis #> 0.88077 0.88077 0.88077 0.88077 0.88077 0.88077 #> pallida parvulus psittacula pauper platyspiza fusca #> 0.88077 0.88077 0.88077 0.88077 0.88077 0.88077 #> pinaroloxias olivacea #> 0.88077 0.88077
The phylo4d
class matches trees with data, or combines them with a data
frame to make a phylo4d
(tree-with-data) object.
Now we'll take the Geospiza data from geospiza_raw$data
and merge it with the tree. First, let's prepare the data:
g1 <- as(geospiza_raw$tree, "phylo4") geodata <- geospiza_raw$data
However, since G. olivacea is included in the tree but not in the data set, we will initially run into some trouble:
g2 <- phylo4d(g1, geodata) #> Error in formatData(phy = x, dt = tip.data, type = "tip", ...): The following nodes are not found in the dataset: olivacea
To deal with G. olivacea missing from the data, we have a few choices. The easiest is to use to allow to create the new object with a warning (you can also use to proceed without warnings):
g2 <- phylo4d(g1, geodata, missing.data="warn") #> Warning in formatData(phy = x, dt = tip.data, type = "tip", ...): The following nodes are #> not found in the dataset: olivacea
Another way to deal with this would be to use prune()
to drop the
offending tip from the tree first:
g1sub <- prune(g1, "olivacea") g1B <- phylo4d(g1sub, geodata)
The difference between the two objects is that the species G. olivacea
is still present in the tree but has no data (i.e., NA
) associated
with it. In the other case, G. olivacea is not included in the tree
anymore. The approach you choose depends on the goal of your analysis.
You can summarize the new object with the function summary
. It breaks
down the statistics about the traits based on whether it is associated
with the tips for the internal nodes: \<\<geomergesum>>= summary(g2) @
Or use tdata()
to extract the data (i.e., tdata(g2)
). By default,
tdata()
will retrieve tip data, but you can also get internal node
data only () or --- if the tip and node data have the same format ---
all the data combined ().
If you want to plot the data (e.g. for checking the input),
plot(tdata(g2))
will create the default plot for the data --- in this
case, since it is a data frame, this will be a pairs
plot of the
data.
The subset
command offers a variety of ways of extracting portions of
a phylo4
or phylo4d
tree, keeping any tip/node data consistent.
tips.include
: give a vector of tips (names or numbers) to retain
tips.exclude
: give a vector of tips (names or numbers) to drop
mrca
: give a vector of node or tip names or numbers; extract the clade containing these taxa
node.subtree
: give a node (name or number); extract the subtree starting from this node
Different ways to extract the fuliginosa-scandens clade:
subset(g2, tips.include=c("fuliginosa", "fortis", "magnirostris", "conirostris", "scandens")) subset(g2, node.subtree=21) subset(g2, mrca=c("scandens", "fortis"))
One could drop the clade by doing
subset(g2, tips.exclude=c("fuliginosa", "fortis", "magnirostris", "conirostris", "scandens")) subset(g2, tips.exclude=names(descendants(g2, MRCA(g2, c("difficilis", "fortis")))))
phylobase
provides many functions that allows users to explore
relationships between nodes on a tree (tree-walking and tree traversal).
Most functions work by specifying the phylo4
(or phylo4d
) object as
the first argument, the node numbers/labels as the second argument
(followed by some additional arguments).
getNode
allows you to find a node based on its node number or its
label. It returns a vector with node numbers as values and labels as
names:
data(geospiza) getNode(geospiza, 10) #> pauper #> 10 getNode(geospiza, "pauper") #> pauper #> 10
If no node is specified, they are all returned, and if a node can't be
found it's returned as a NA
. It is possible to control what happens
when a node can't be found:
getNode(geospiza) #> fuliginosa fortis magnirostris conirostris scandens difficilis #> 1 2 3 4 5 6 #> pallida parvulus psittacula pauper Platyspiza fusca #> 7 8 9 10 11 12 #> Pinaroloxias olivacea N15 N16 N17 N18 #> 13 14 15 16 17 18 #> N19 N20 N21 N22 N23 N24 #> 19 20 21 22 23 24 #> N25 N26 N27 #> 25 26 27 getNode(geospiza, 10:14) #> pauper Platyspiza fusca Pinaroloxias olivacea #> 10 11 12 13 14 getNode(geospiza, "melanogaster", missing="OK") # no warning #> <NA> #> NA getNode(geospiza, "melanogaster", missing="warn") # warning! #> Warning in getNode(geospiza, "melanogaster", missing = "warn"): Some nodes not found #> among all nodes in tree: melanogaster #> <NA> #> NA
children
and ancestor
give the immediate neighboring nodes:
children(geospiza, 16) #> N17 Pinaroloxias #> 17 13 ancestor(geospiza, 16) #> N15 #> 15
while descendants
and ancestors
can traverse the tree up to the tips
or root respectively:
descendants(geospiza, 16) # by default returns only the tips #> Pinaroloxias fusca Platyspiza difficilis scandens conirostris #> 13 12 11 6 5 4 #> magnirostris fuliginosa fortis pallida pauper parvulus #> 3 1 2 7 10 8 #> psittacula #> 9 descendants(geospiza, "all") # also include the internal nodes #> Warning in getNode(phy, node, missing = "warn"): Some nodes not found among all nodes in #> tree: all #> named list() ancestors(geospiza, 20) #> N19 N18 N17 N16 N15 #> 19 18 17 16 15 ancestors(geospiza, 20, "ALL") # uppercase ALL includes self #> N20 N19 N18 N17 N16 N15 #> 20 19 18 17 16 15
siblings
returns the other node(s) associated with the same ancestor:
siblings(geospiza, 20) #> N25 #> 25 siblings(geospiza, 20, include.self=TRUE) #> N20 N25 #> 20 25
MRCA
returns the most common recent ancestor for a set of tips, and
shortest path returns the nodes connecting 2 nodes:
MRCA(geospiza, 1:6) #> N20 #> 20 shortestPath(geospiza, 4, "pauper") #> N19 N20 N21 N22 N25 N26 #> 19 20 21 22 25 26
multiPhylo4
classes are not yet implemented but will be coming soon.
This section will describe a way of constructing a simulator that generates trait values for extant species (tips) given a tree with branch lengths, assuming a model of Brownian motion.
We can use to coerce the tree into a variance-covariance matrix form,
and then use mvrnorm
from the MASS
package to generate a set of
multivariate normally distributed values for the tips. (A benefit of
this approach is that we can very quickly generate a very large number
of replicates.) This example illustrates a common feature of working
with phylobase
--- combining tools from several different packages to
operate on phylogenetic trees with data.
We start with a randomly generated tree using rcoal()
from ape
to
generate the tree topology and branch lengths:
set.seed(1001) tree <- as(rcoal(12), "phylo4")
Next we generate the phylogenetic variance-covariance matrix (by
coercing the tree to a phylo4vcov
object) and pick a single set of
normally distributed traits (using to pick a multivariate normal deviate
with a variance-covariance matrix that matches the structure of the
tree).
vmat <- as(tree, "phylo4vcov") vmat <- cov2cor(vmat) library(MASS) trvec <- mvrnorm(1, mu=rep(0, 12), Sigma=vmat)
The last step (easy) is to convert the phylo4vcov
object back to a
phylo4d
object:
treed <- phylo4d(tree, tip.data=as.data.frame(trvec)) plot(treed)
This section details the internal structure of the phylo4
,
multiphylo4
(coming soon!), phylo4d
, and multiphylo4d
(coming
soon!) classes. The basic building blocks of these classes are the
phylo4
object and a dataframe. The phylo4
tree format is largely
similar to the one used by phylo
class in the package ape
^1.
We use "edge" for ancestor-descendant relationships in the phylogeny (sometimes called "branches") and "edge lengths" for their lengths ("branch lengths"). Most generally, "nodes" are all species in the tree; species with descendants are "internal nodes" (we often refer to these just as "nodes", meaning clear from context); "tips" are species with no descendants. The "root node" is the node with no ancestor (if one exists).
Like phylo
, the main components of the phylo4
class are:
edge
: a 2-column matrix of integers, with $N$ rows for a rooted tree or
$N-1$ rows for an unrooted tree and column names ancestor
and
descendant
. Each row contains information on one edge in the tree.
See below for further constraints on the edge matrix.
edge.length
: numeric list of edge lengths (length $N$ (rooted) or $N-1$ (unrooted) or empty (length 0))
tip.label
: character vector of tip labels (required), with length=# of tips. Tip labels need not be unique, but data-tree matching with non-unique labels will cause an error
node.label
: character vector of node labels, length=# of internal nodes or 0 (if empty). Node labels need not be unique, but data-tree matching with non-unique labels will cause an error
order
: character: "preorder", "postorder", or "unknown" (default),
describing the order of rows in the edge matrix. , "pruningwise" and
"cladewise" are accepted for compatibility with ape
The edge matrix must not contain NA
s, with the exception of the root
node, which has an NA
for ancestor
. phylobase
does not enforce an
order on the rows of the edge matrix, but it stores information on the
current ordering in the slot --- current allowable values are "unknown"
(the default), "preorder" (equivalent to "cladewise" in ape
) or
"postorder" [^2].
The basic criteria for the edge matrix are similar to those of ape
, as
documented it's tree specification^3. This is a modified version of
those rules, for a tree with $n$ tips and $m$ internal nodes:
Tips (no descendants) are coded $1,\ldots, n$, and internal nodes ($\ge 1$ descendant) are coded $n + 1, \ldots , n + m$ ($n + 1$ is the root). Both series are numbered with no gaps.
The first (ancestor) column has only values $> n$ (internal nodes): thus, values $\le n$ (tips) appear only in the second (descendant) column
all internal nodes (not including the root) must appear in the
first (ancestor) column at least once [unlike ape
, which
nominally requires each internal node to have at least two
descendants (although it doesn't absolutely prohibit them and has a
function to get rid of them), phylobase
does allow these
"singleton nodes" and has a method hasSingle
for detecting them].
Singleton nodes can be useful as a way of representing changes along
a lineage; they are used this way in the ouch
package.
the number of occurrences of a node in the first column is related to the nature of the node: once if it is a singleton, twice if it is dichotomous (i.e., of degree 3 [counting ancestor as well as descendants]), three times if it is trichotomous (degree 4), and so on.
phylobase
does not technically prohibit reticulations (nodes or tips
that appear more than once in the descendant column), but they will
probably break most of the methods. Disconnected trees, cycles, and
other exotica are not tested for, but will certainly break the methods.
We have defined basic methods for phylo4
:show
, print
, and a
variety of accessor functions (see help files). summary
does not seem
to be terribly useful in the context of a "raw" tree, because there is
not much to compute.
The phylo4d
class extends phylo4
with data. Tip data, and (internal)
node data are stored separately, but can be retrieved together or
separately with tdata(x,"tip")
, tdata(x,"internal")
or
tdata(x,"all")
. There is no separate slot for edge data, but these can
be stored as node data associated with the descendant node.
[^2]: see https://en.wikipedia.org/wiki/Tree_traversal for more
information on orderings. (ape
's "pruningwise" is "bottom-up"
ordering).
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