Provided by: libbio-perl-perl_1.7.2-2_all
NAME
Bio::Tree::Statistics - Calculate certain statistics for a Tree
SYNOPSIS
use Bio::Tree::Statistics;
DESCRIPTION
This should be where Tree statistics are calculated. It was previously where statistics from a Coalescent simulation. It now contains several methods for calculating Tree-Trait statistics.
FEEDBACK
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AUTHOR - Jason Stajich
Email jason AT bioperl.org
CONTRIBUTORS
Heikki Lehvaslaiho, heikki at bioperl dot org
APPENDIX
The rest of the documentation details each of the object methods. Internal methods are usually preceded with a _ new Title : new Usage : my $obj = Bio::Tree::Statistics->new(); Function: Builds a new Bio::Tree::Statistics object Returns : Bio::Tree::Statistics Args : assess_bootstrap Title : assess_bootstrap Usage : my $tree_with_bs = $stats->assess_bootstrap(\@bs_trees,$guide_tree); Function: Calculates the bootstrap for internal nodes based on the percentage of times \@bs_trees agree with each internal node Returns : L<Bio::Tree::TreeI> Args : Arrayref of L<Bio::Tree::TreeI>s Guide tree, L<Bio::Tree::TreeI>s cherries Example : cherries($tree, $node); Description: Count number of paired leaf nodes in a binary tree Returns : integer Exceptions : Args : 1. Bio::Tree::TreeI object 2. Bio::Tree::NodeI object within the tree, optional Commonly used statistics assume a binary tree, but this methods returns a value even for trees with polytomies. Tree-Trait statistics The following methods produce descriptors of trait distribution among leaf nodes within the trees. They require that a trait has been set for each leaf node. The tag methods of Bio::Tree::Node are used to store them as key/value pairs. In this way, one tree can store more than one trait. Trees have method add_traits() to set trait values from a file. See the add_trait() method in Bio::Tree::TreeFunctionsI. fitch Example : fitch($tree, $key, $node); Description: Calculates Parsimony Score (PS) and internal trait values using the Fitch 1971 parsimony algorithm for the subtree a defined by the (internal) node. Node defaults to the root. Returns : true on success Exceptions : leaf nodes have to have the trait defined Args : 1. Bio::Tree::TreeI object 2. trait name string 3. Bio::Tree::NodeI object within the tree, optional Runs first fitch_up that calculates parsimony scores and then fitch_down that should resolve most of the trait/character state ambiguities. Fitch, W.M., 1971. Toward defining the course of evolution: minimal change for a specific tree topology. Syst. Zool. 20, 406-416. You can access calculated parsimony values using: $score = $node->->get_tag_values('ps_score'); and the trait value with: $traitvalue = $node->->get_tag_values('ps_trait'); # only the first @traitvalues = $node->->get_tag_values('ps_trait'); Note that there can be more that one trait value, especially for the root node. ps Example : ps($tree, $key, $node); Description: Calculates Parsimony Score (PS) from Fitch 1971 parsimony algorithm for the subtree as defined by the (internal) node. Node defaults to the root. Returns : integer, 1 < PS < n, where n is number of branches Exceptions : leaf nodes have to have the trait defined Args : 1. Bio::Tree::TreeI object 2. trait name string 3. Bio::Tree::NodeI object within the tree, optional This is the first half of the Fitch algorithm that is enough for calculating the resolved parsimony values. The trait/chararacter states are commonly left in ambiguous state. To resolve them, run fitch_down. fitch_up Example : fitch_up($tree, $key, $node); Description: Calculates Parsimony Score (PS) from the Fitch 1971 parsimony algorithm for the subtree as defined by the (internal) node. Node defaults to the root. Returns : integer, 1< PS < n, where n is number of branches Exceptions : leaf nodes have to have the trait defined Args : 1. Bio::Tree::TreeI object 2. trait name string 3. Bio::Tree::NodeI object within the tree, optional This is a more generic name for ps and indicates that it performs the first bottom-up tree traversal that calculates the parsimony score but usually leaves trait/character states ambiguous. If you are interested in internal trait states, running fitch_down should resolve most of the ambiguities. fitch_down Example : fitch_down($tree, $node); Description: Runs the second pass from Fitch 1971 parsimony algorithm to resolve ambiguous trait states left by first pass. by the (internal) node. Node defaults to the root. Returns : true Exceptions : dies unless the trait is defined in all nodes Args : 1. Bio::Tree::TreeI object 2. Bio::Tree::NodeI object within the tree, optional Before running this method you should have ran fitch_up (alias to ps ). Note that it is not guaranteed that all states are completely resolved. persistence Example : persistence($tree, $node); Description: Calculates the persistence for node in the subtree defined by the (internal) node. Node defaults to the root. Returns : int, number of generations trait value has to remain same Exceptions : all the nodes need to have the trait defined Args : 1. Bio::Tree::TreeI object 2. Bio::Tree::NodeI object within the tree, optional Persistence measures the stability that the trait value has in a tree. It expresses the number of generations the trait value remains the same. All the decendants of the root in the same generation have to share the same value. Depends on Fitch's parsimony score (PS). count_subclusters Example : count_clusters($tree, $node); Description: Calculates the number of sub-clusters in the subtree defined by the (internal) node. Node defaults to the root. Returns : int, count Exceptions : all the nodes need to have the trait defined Args : 1. Bio::Tree::TreeI object 2. Bio::Tree::NodeI object within the tree, optional Depends on Fitch's parsimony score (PS). count_leaves Example : count_leaves($tree, $node); Description: Calculates the number of leaves with same trait value as root in the subtree defined by the (internal) node. Requires an unbroken line of identical trait values. Node defaults to the root. Returns : int, number of leaves with this trait value Exceptions : all the nodes need to have the trait defined Args : 1. Bio::Tree::TreeI object 2. Bio::Tree::NodeI object within the tree, optional Depends on Fitch's parsimony score (PS). phylotype_length Example : phylotype_length($tree, $node); Description: Sums up the branch lengths within phylotype exluding the subclusters where the trait values are different Returns : float, length Exceptions : all the nodes need to have the trait defined Args : 1. Bio::Tree::TreeI object 2. Bio::Tree::NodeI object within the tree, optional Depends on Fitch's parsimony score (PS). sum_of_leaf_distances Example : sum_of_leaf_distances($tree, $node); Description: Sums up the branch lengths from root to leaf exluding the subclusters where the trait values are different Returns : float, length Exceptions : all the nodes need to have the trait defined Args : 1. Bio::Tree::TreeI object 2. Bio::Tree::NodeI object within the tree, optional Depends on Fitch's parsimony score (PS). genetic_diversity Example : genetic_diversity($tree, $node); Description: Diversity is the sum of root to leaf distances within the phylotype normalised by number of leaf nodes Returns : float, value of genetic diversity Exceptions : all the nodes need to have the trait defined Args : 1. Bio::Tree::TreeI object 2. Bio::Tree::NodeI object within the tree, optional Depends on Fitch's parsimony score (PS). statratio Example : statratio($tree, $node); Description: Ratio of the stem length and the genetic diversity of the phylotype L<genetic_diversity> Returns : float, separation score Exceptions : all the nodes need to have the trait defined Args : 1. Bio::Tree::TreeI object 2. Bio::Tree::NodeI object within the tree, optional Statratio gives a measure of separation and variability within the phylotype. Larger values identify more rapidly evolving and recent phylotypes. Depends on Fitch's parsimony score (PS). ai Example : ai($tree, $key, $node); Description: Calculates the Association Index (AI) of Whang et al. 2001 for the subtree defined by the (internal) node. Node defaults to the root. Returns : real Exceptions : leaf nodes have to have the trait defined Args : 1. Bio::Tree::TreeI object 2. trait name string 3. Bio::Tree::NodeI object within the tree, optional Association index (AI) gives a more fine grained results than PS since the result is a real number. ~0 E<lt>= AI. Wang, T.H., Donaldson, Y.K., Brettle, R.P., Bell, J.E., Simmonds, P., 2001. Identification of shared populations of human immunodeficiency Virus Type 1 infecting microglia and tissue macrophages outside the central nervous system. J. Virol. 75 (23), 11686-11699. mc Example : mc($tree, $key, $node); Description: Calculates the Monophyletic Clade (MC) size statistics for the subtree a defined by the (internal) node. Node defaults to the root; Returns : hashref with trait values as keys Exceptions : leaf nodes have to have the trait defined Args : 1. Bio::Tree::TreeI object 2. trait name string 3. Bio::Tree::NodeI object within the tree, optional Monophyletic Clade (MC) size statistics by Salemi at al 2005. It is calculated for each trait value. 1 E<lt>= MC E<lt>= nx, where nx is the number of tips with value x: pick the internal node with maximim value for number of of tips with only trait x MC was defined by Parker et al 2008. Salemi, M., Lamers, S.L., Yu, S., de Oliveira, T., Fitch, W.M., McGrath, M.S., 2005. Phylodynamic analysis of Human Immunodeficiency Virus Type 1 in distinct brain compartments provides a model for the neuropathogenesis of AIDS. J. Virol. 79 (17), 11343-11352. Parker, J., Rambaut A., Pybus O., 2008. Correlating viral phenotypes with phylogeny: Accounting for phylogenetic uncertainty Infection, Genetics and Evolution 8 (2008), 239-246.