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* Bio.Phylo.[[PAML]] provides wrappers, parsers and utilities for working with the PAML suite of programs.
* Bio.Phylo.[[PAML]] provides wrappers, parsers and utilities for working with the PAML suite of programs.
See the [http://biopython.org/DIST/docs/tutorial/Tutorial.html Biopython Tutorial] sections on sequence alignment and BLAST for explanations of the first few steps shown here.
See the [http://biopython.org/DIST/docs/tutorial/Tutorial.html Biopython Tutorial] sections on sequence alignment and BLAST for explanations of the first few steps shown here.
Latest revision as of 13:49, 16 January 2014
This module provides classes, functions and I/O support for working with phylogenetic trees.
For more complete documentation, see the Phylogenetics chapter of the Biopython Tutorial and the Bio.Phylo API pages generated from the source code. The Phylo cookbook page has more examples of how to use this module, and the PhyloXML page describes how to attach graphical cues and additional information to a tree.
This module is included in Biopython 1.54 and later. If you're interested in testing newer additions to this code before the next official release, see SourceCode for instructions on getting a copy of the development branch.
To draw trees (optional), you'll also need these packages:
- NetworkX -- for the functions 'draw_graphviz' and 'to_networkx'
- PyGraphviz or pydot -- for the functions 'draw_graphviz' and 'to_networkx'
The I/O and tree-manipulation functionality will work without them; they're imported on demand when the functions draw(), draw_graphviz() and to_networkx() are called.
To use this module in older versions of Biopython with Python 2.4, you'll also need to install a separate package that provides the ElementTree interface for XML parsing. Either of these will work:
The Phylo module has also been successfully tested on Jython 2.5.1, minus the Graphviz- and NetworkX-based functions. However, parsing phyloXML files is noticeably slower because Jython uses a different version of the underlying XML parsing library.
Wrappers for supported file formats are available from the top level of the module:
from Bio import Phylo
Like SeqIO and AlignIO, this module provides four I/O functions: parse(), read(), write() and convert(). Each function accepts either a file name or an open file handle, so data can be also loaded from compressed files, StringIO objects, and so on. If the file name is passed as a string, the file is automatically closed when the function finishes; otherwise, you're responsible for closing the handle yourself.
The second argument to each function is the target format. Currently, the following formats are supported:
See the PhyloXML page for more examples of using tree objects.
Incrementally parse each tree in the given file or handle, returning an iterator of Tree objects (i.e. some subclass of the Bio.Phylo.BaseTree Tree class, depending on the file format).
>>> trees = Phylo.parse('phyloxml_examples.xml', 'phyloxml') >>> for tree in trees: ... print tree.name
example from Prof. Joe Felsenstein's book "Inferring Phylogenies" example from Prof. Joe Felsenstein's book "Inferring Phylogenies" same example, with support of type "bootstrap" same example, with species and sequence same example, with gene duplication information and sequence relationships similar example, with more detailed sequence data network, node B is connected to TWO nodes: AB and C ...
If there's only one tree, then the next() method on the resulting generator will return it.
>>> tree = Phylo.parse('phyloxml_examples.xml', 'phyloxml').next() >>> tree.name 'example from Prof. Joe Felsenstein\'s book "Inferring Phylogenies"'
Note that this doesn't immediately reveal whether there are any remaining trees -- if you want to verify that, use read() instead.
Parse and return exactly one tree from the given file or handle. If the file contains zero or multiple trees, a ValueError is raised. This is useful if you know a file contains just one tree, to load that tree object directly rather than through parse() and next(), and as a safety check to ensure the input file does in fact contain exactly one phylogenetic tree at the top level.
tree = Phylo.read('example.dnd', 'newick') print tree
If you have your tree data already loaded as a Python string, you can parse it with the help of StringIO (in Python's standard library):
from cStringIO import StringIO treedata = "(A, (B, C), (D, E))" handle = StringIO(treedata) tree = Phylo.read(handle, "newick")
In one line:
tree = Phylo.read(StringIO("(A, (B, C), (D, E))"), "newick")
The other I/O functions also can be used with StringIO.
(General tip: if you write to the StringIO object and want to re-read the contents, you'll need to call the
seek(0) method to move the handle back to the start of the StringIO data -- the same as an open file handle. See examples of this in the unit tests for Phylo,
Tests/test_Phylo.py, in the Biopython source code.)
Write a sequence of Tree objects to the given file or handle. Passing a single Tree object instead of a list or iterable will also work. (See, Phylo is friendly.)
tree1 = Phylo.read('example1.xml', 'phyloxml') tree2 = Phylo.read('example2.xml', 'phyloxml') Phylo.write([tree1, tree2], 'example-both.xml', 'phyloxml')
Given two files (or handles) and two formats, both supported by Bio.Phylo, convert the first file from the first format to the second format, writing the output to the second file.
Phylo.convert('example.nhx', 'newick', 'example2.nex', 'nexus')
Within the Phylo module are parsers and writers for specific file formats, conforming to the basic top-level API and sometimes adding additional features.
NeXMLIO: Support for the NeXML format.
NewickIO: A port of the parser in Bio.Nexus.Trees to support the Newick (a.k.a. New Hampshire) format through the Phylo API.
NexusIO: Wrappers around Bio.Nexus to support the Nexus tree format.
CDAOIO: Support for the Comparative Data Analysis Ontology (CDAO). Requires RDFlib.
The Nexus format actually contains several sub-formats for different kinds of data; to represent trees, Nexus provides a block containing some metadata and one or more Newick trees. (Another kind of Nexus block can represent alignments; this is handled in AlignIO.) So to parse a complete Nexus file with all block types handled, use Bio.Nexus directly, and to extract just the trees, use Bio.Phylo.
Tree and Subtree classes
The basic objects are defined in Bio.Phylo.BaseTree.
To support additional information stored in specific file formats, sub-modules within Tree offer additional classes that inherit from BaseTree classes.
Each sub-class of BaseTree.Tree or Node has a class method to promote an object from the basic type to the format-specific one. These sub-class objects can generally be treated as instances of the basic type without any explicit conversion.
PhyloXML: Support for the phyloXML format. See the PhyloXML page for details.
Newick: The Newick module provides minor enhancements to the BaseTree classes, plus several shims for compatibility with the existing Bio.Nexus module. The API for this module is under development and should not be relied on, other than the functionality already provided by BaseTree.
Some additional tools are located in the Utils module under Bio.Phylo. These functions are also loaded to the top level of the Phylo module on import for easy access.
Where a third-party package is required, that package is imported when the function itself is called, so these dependencies are not necessary to install or use the rest of the Tree module.
str(tree) produces a plain-text representation of the entire tree. Strings are automatically truncated to ensure reasonable display.
Use this with the print statement to get a quick overview of your tree:
>>> tree = Phylo.parse('phyloxml_examples.xml', 'phyloxml').next() >>> print tree Phylogeny(description='phyloXML allows to use either a "branch_length" attribute or element to indicate branch lengths.', name='example from Prof. Joe Felsenstein's book "Inferring Phylogenies"') Clade() Clade(branch_length=0.06) Clade(branch_length=0.102, name='A') Clade(branch_length=0.23, name='B') Clade(branch_length=0.4, name='C') ...
draw displays a rooted phylogram using matplotlib or pylab. New in Biopython 1.58.
tree = Phylo.read('apaf.xml', 'phyloxml') tree.ladderize() # Flip branches so deeper clades are displayed at top Phylo.draw(tree)
draw_graphviz mimics the networkx function of the same name, with some tweaks to improve the display of the graph. If a file name is given, the graph is drawn directly to that file, and options such as image format (default PDF) may be used.
Drawing a basic dendrogram is simple:
import pylab tree = Phylo.read('apaf.xml', 'phyloxml') Phylo.draw_graphviz(tree) pylab.show()
Here's the same tree without the circles at each labelled node:
See the Phylo cookbook page for more drawing features and options.
draw_ascii prints an ascii-art rooted phylogram to standard output, or another file handle if specified. Only terminal node labels are shown; these are the result of str(clade) (usually clade names). The width of the text field used for drawing is 80 characters by default, adjustable with the column_width keyword argument, and the height in character rows is twice the number of terminals in the tree.
A simple tree with defined branch lengths looks like this:
>>> tree = Phylo.parse('phyloxml_examples.xml', 'phyloxml').next() >>> Phylo.draw_ascii(tree) _____________ A _______| _| |_______________________________ B | |_______________________________________________________ C
The same topology without branch lengths is drawn with equal-length branches:
___________________________ A ___________________________| _| |___________________________ B | |___________________________ C
A larger tree (apaf.xml, 31 leaf nodes) drawn with the default column width demonstrates how relatively short branches are handled:
>>> apaf = Phylo.read('apaf.xml', 'phyloxml') >>> Phylo.draw_ascii(apaf) _ 22_MOUSE | _| Apaf-1_HUMAN | | ,| | 12_CANFA || _||___ 11_CHICK | | | |___________ 16_XENLA _______| | | , 14_FUGRU | | __| | |____| |__ 15_TETNG _____| | | | |____ 17_BRARE | | | | ______ 1_BRAFL | | __| ______| || |_________ 18_NEMVE | | | | | |____________ 23_STRPU | | _| | _________ 26_STRPU | | |_________| | | |________ 25_STRPU | | | | ___ CED4_CAEEL | |___________________________________| ____| |_ 31_CAEBR | | | | ___ 28_DROPS | | _____________________| | | ______| |____ Dark_DROME | | | | | |__| |_______________________ 29_AEDAE | | | |__________________________ 30_TRICA | | _ 34_BRAFL | _________________________| _| _____| |_ 35_BRAFL | | | | __| |_______________ 8_BRAFL | | | | | | ___________________ 20_NEMVE | ______________| |_______| | | | |__________________________ 21_NEMVE | | | | ___| |______________________________ 9_BRAFL | | | | | | _____________ 3_BRAFL | | | _____| | | |_________| |_________________ 2_BRAFL |____| | | |_______________ 19_NEMVE | | _____ 37_BRAFL | ________________________| |___________| |____ 36_BRAFL | |______________________ 33_BRAFL
Exporting to other object representations
Although any phylogenetic tree can reasonably be represented by a directed acyclic graph, the Phylo module does not attempt to provide a generally usable graph library -- only the minimum functionality to represent phylogenetic trees. Instead, it provides functions for exporting tree objects to the standard graph representations, adjacency list (dict) and adjacency matrix, using third-party libraries.
to_networkx returns the given tree as a NetworkX LabeledDiGraph or LabeledGraph object (depending on whether the tree is rooted). You'll probably need to import networkx directly for subsequent operations on the graph object. From this point you can also try using one of networkx's drawing functions to display the tree, and for simple, fully labeled trees it may even work -- but you'll have better results with Phylo's own draw_graphviz function, discussed above.
import networkx, pylab tree = Phylo.read('example.xml', 'phyloxml') net = Phylo.to_networkx(tree) networkx.draw(net) pylab.show()
Recipes for exporting to other libraries, including ape (via Rpy2) and PyCogent, are available on the Phylo cookbook page.
Upcoming GSoC 2013 features
Many new features for building and processing phylogenetic trees were developed by Yanbo Ye for Google Summer of Code 2013. They are available on the development branch (see SourceCode) but are not yet included in an official Biopython release version. Note that the behavior and API of these features may change before the upcoming official release.
In addition to wrappers of tree construction programs(PHYLIP programs through EMBOSS wrappers in Bio.Emboss.Applications), now Biopython also provides several tree construction algorithm implementations in pure python in the
All algorithms are designed as worker subclasses of a base class
TreeConstructor. All constructors have the same method
build_tree that accept a
MultipleSeqAlignment object to construct the tree. Currently there are two types of tree constructors:
DistanceTreeConstructor has two algorithms: UPGMA(Unweighted Pair Group Method with Arithmetic Mean) and NJ(Neighbor Joining).
Both algorithms construct trees based on a distance matrix. So before using these algorithms, let me introduce the
DistanceCalculator to generate the distance matrix from a
MultipleSeqAlignment object. The following code shows a common way to do this:
>>> from Bio.Phylo.TreeConstruction import DistanceCalculator >>> from Bio import AlignIO >>> aln = AlignIO.read('Tests/TreeConstruction/msa.phy', 'phylip') >>> print aln SingleLetterAlphabet() alignment with 5 rows and 13 columns AACGTGGCCACAT Alpha AAGGTCGCCACAC Beta GAGATTTCCGCCT Delta GAGATCTCCGCCC Epsilon CAGTTCGCCACAA Gamma >>> calculator = DistanceCalculator('identity') >>> dm = calculator.get_distance(aln) >>> dm DistanceMatrix(names=['Alpha', 'Beta', 'Gamma', 'Delta', 'Epsilon'], matrix=[, [0.23076923076923073, 0], [0.3846153846153846, 0.23076923076923073, 0], [0.5384615384615384, 0.5384615384615384, 0.5384615384615384, 0], [0.6153846153846154, 0.3846153846153846, 0.46153846153846156, 0.15384615384615385, 0]]) >>> print dm Alpha 0 Beta 0.230769230769 0 Gamma 0.384615384615 0.230769230769 0 Delta 0.538461538462 0.538461538462 0.538461538462 0 Epsilon 0.615384615385 0.384615384615 0.461538461538 0.153846153846 0 Alpha Beta Gamma Delta Epsilon
As you see, we create a
DistanceCalculator object with a string 'identity', which is the name of the model(scoring matrix) to calculate the distance. The 'identity' model is the default one and can be used both for DNA and Protein sequence. To check available models for DNA, protein or all, use the attribute of the calculator
After the calculator is created with the model, simply use the
get_distance() method to get the distance matrix of a given alignment object. Then you will get a
DistanceMatrix object, a subclass of
Matrix(we will talk about this later).
Now, let's get back to the
DistanceTreeConstructor. We can pass the
DistanceCalculator object and a string parameter('nj' or 'upgma') to initialize it, and then call its
build_tree() as mentioned before.
>>> from TreeConstruction import DistanceTreeConstructor >>> constructor = DistanceTreeConstructor(calculator, 'nj') >>> tree = constructor.build_tree(aln) >>> print tree Tree(rooted=False) Clade(branch_length=0, name='Inner3') Clade(branch_length=0.182692307692, name='Alpha') Clade(branch_length=0.0480769230769, name='Beta') Clade(branch_length=0.0480769230769, name='Inner2') Clade(branch_length=0.278846153846, name='Inner1') Clade(branch_length=0.0512820512821, name='Epsilon') Clade(branch_length=0.102564102564, name='Delta') Clade(branch_length=0.144230769231, name='Gamma')
While sometimes you might want to use your own
DistanceMatrix directly instead of the raw alignment, we provide another direct way to use both algorithms.
>>> from TreeConstruction import DistanceTreeConstructor >>> constructor = DistanceTreeConstructor() >>> tree = constructor.nj(dm) >>> print tree Tree(rooted=False) Clade(branch_length=0, name='Inner3') Clade(branch_length=0.182692307692, name='Alpha') Clade(branch_length=0.0480769230769, name='Beta') Clade(branch_length=0.0480769230769, name='Inner2') Clade(branch_length=0.278846153846, name='Inner1') Clade(branch_length=0.0512820512821, name='Epsilon') Clade(branch_length=0.102564102564, name='Delta') Clade(branch_length=0.144230769231, name='Gamma') >>> tree = constructor.upgma(dm) >>> print tree Tree(rooted=True) Clade(branch_length=0, name='Inner4') Clade(branch_length=0.1875, name='Inner1') Clade(branch_length=0.0769230769231, name='Epsilon') Clade(branch_length=0.0769230769231, name='Delta') Clade(branch_length=0.110576923077, name='Inner3') Clade(branch_length=0.0384615384615, name='Inner2') Clade(branch_length=0.115384615385, name='Gamma') Clade(branch_length=0.115384615385, name='Beta') Clade(branch_length=0.153846153846, name='Alpha')
DistanceTreeConstructor, the concrete algorithm of
ParsimonyTreeConstructor is delegated to two different worker classes: the
ParsimonyScorer to calculate the parsimony score of a target tree by the given alignment, and the
TreeSearcher to search the best tree that minimize the parsimony score. A typical usage example can be as follows:
>>> from Bio import AlignIO >>> from TreeConstruction import * >>> aln = AlignIO.read(open('Tests/TreeConstruction/msa.phy'), 'phylip') >>> starting_tree = Phylo.read('Tests/TreeConstruction/nj.tre', 'newick') >>> scorer = ParsimonyScorer() >>> searcher = NNITreeSearcher(scorer) >>> constructor = ParsimonyTreeConstructor(searcher, starting_tree) >>> pars_tree = constructor.build_tree(aln) >>> print pars_tree Tree(weight=1.0, rooted=True) Clade(branch_length=0.0) Clade(branch_length=0.197335, name='Inner1') Clade(branch_length=0.13691, name='Delta') Clade(branch_length=0.08531, name='Epsilon') Clade(branch_length=0.041935, name='Inner2') Clade(branch_length=0.01421, name='Inner3') Clade(branch_length=0.17523, name='Gamma') Clade(branch_length=0.07477, name='Beta') Clade(branch_length=0.29231, name='Alpha')
ParsimonyScorer is a combination of the Fitch algorithm and Sankoff algorithm. It will work as Fitch algorithm by default if no parameter is provide, and work as Sankoff algorithm if a parsimony scoring matrix(a
Matrix object) is given, .
Then the scorer is passed to a
TreeSearcher to tell it how to evaluate different trees during searching. Currently, only one searcher
NNITreeSearcher, the Nearest Neighbor Interchange(NNI) algorithm, is implemented.
By passing the searcher and a starting tree to the
ParsimonyTreeConstructor, we finally get the instance of it. If no starting tree is provided, a simple upgma tree will be created instead, with the 'identity' model. To use this parsimony constructor, just simply call the
build_tree method with an alignment.
Strict, Majority Rule and Adam Consensus
Same as tree construction algorithms, three consensus tree algorithms(Strict, Majority Rule and Adam Consensus) in pure python are also implemented in the
Bio.Phylo.Consensus module. You can directly call
adam_consensus to use these algorithms with a list of trees as the input.
>>> from Bio import Phylo >>> from Bio.Phylo.Consensus import * >>> trees = list(Phylo.parse('Tests/TreeConstruction/trees.tre', 'newick')) >>> strict_tree = strict_consensus(trees) >>> majority_tree = majority_consensus(trees, 0.5) >>> adam_tree = adam_consensus(trees)
Instead of using 50% as the cutoff, the
majority_consensus method allows you to set your own one by providing an extra
cutoff parameter(0~1, 0 by default). That means it can also work as strict consensus algorithm when the
cutoff equals 1. One more thing different to strict and adam consensus tree, the result majority rule consensus tree has branch support value that are automatically assigned during calculation.
To get the consensus tree, we must construct a list of bootstrap replicate trees. So in the
Bio.Phylo.Consensus module, we also provide several useful bootstrap methods to achieve this.
>>> from Bio import Phylo >>> from Bio.Phylo.Consensus import * >>> msa = AlignIO.read('Tests/TreeConstruction/msa.phy', 'phylip') >>> msas = bootstrap(msa, 100)
As you see, the
bootstrap method accepts a
MultipleSeqAlignment object and generates its bootstrap replicate 100 times. The you can use them to build replicate trees. While, we also provide a convenient method to do this.
>>> calculator = DistanceCalculator('blosum62') >>> constructor = DistanceTreeConstructor(calculator) >>> trees = bootstrap_trees(msa, 100, constructor)
This time we pass an extra
DistanceTreeConstructor object to a
bootstrap_trees method and finally got the replicate trees. Note that both
bootstrap_trees are generator functions. You need to use
list() function to turn the result into a list of alignment or trees.
Another useful function is
bootstrap_consensus. By passing the consensus method as another extra parameter, we can directly get the consensus tree.
>>> consensus_tree = bootstrap_consensus(msa, 100, constructor, majority_consensus)
To get the branch support of a specific tree, we can use the
>>> from Bio import Phylo >>> from Bio.Phylo.Consensus import * >>> trees = list(Phylo.parse('Tests/TreeConstruction/trees.tre', 'newick')) >>> target_tree = trees >>> support_tree = get_support(target_tree, trees)
In the above code, we use the first tree as the target tree that we want to calculate its branch support. The
get_support method accepts the target tree and a list of trees, and returns a tree, with all internal clades assigned with branch support values.
Other Useful Classes
There are some other classes in both
Consensus module that are used in those algorithms. They may not be used commonly, but might be useful to you in some cases.
_Matrix class in the
TreeConstruction module is the super class of
_DistanceMatrix. They are both actually constructed by a list of names and a nested list of numbers in lower triangular matrix format. The only difference between them is that the diagonal elements in
_DistanceMatrix will all be 0 no matter what values are assigned.
To create a
>>> from Bio.Phylo.TreeConstruction import _Matrix >>> names = ['Alpha', 'Beta', 'Gamma', 'Delta'] >>> matrix = [, [1, 0], [2, 3, 0], [4, 5, 6, 0]] >>> m = _Matrix(names, matrix) >>> m _Matrix(names=['Alpha', 'Beta', 'Gamma', 'Delta'], matrix=[, [1, 0], [2, 3, 0], [4, 5, 6, 0]]) >>> print m Alpha 0 Beta 1 0 Gamma 2 3 0 Delta 4 5 6 0 Alpha Beta Gamma Delta
You can use two indices to get or assign an element in the matrix, and the indices are exchangeable.
>>> m[1,2] 3 >>> m[2,1] 3 >>> m['Beta','Gamma'] 3 >>> m['Beta','Gamma'] = 4 >>> m['Beta','Gamma'] 4
Further more, you can use one index to get or assign a list of elements related to that index:
>>> m [0, 1, 2, 4] >>> m['Alpha'] [0, 1, 2, 4] >>> m['Alpha'] = [0, 7, 8, 9] >>> m [0, 7, 8, 9] >>> m[0,1] 7
Also you can delete or insert a column&row of elements by index:
>>> m _Matrix(names=['Alpha', 'Beta', 'Gamma', 'Delta'], matrix=[, [7, 0], [8, 4, 0], [9, 5, 6, 0]]) >>> del m['Alpha'] >>> m _Matrix(names=['Beta', 'Gamma', 'Delta'], matrix=[, [4, 0], [5, 6, 0]]) >>> m.insert('Alpha', [0, 7, 8, 9] , 0) >>> m _Matrix(names=['Alpha', 'Beta', 'Gamma', 'Delta'], matrix=[, [7, 0], [8, 4, 0], [9, 5, 6, 0]])
_BitString is an assistant class used frequently in the algorithms in the
Consensus module. It's a sub-class of
str object that only accepts two characters('0' and '1'), with additional functions for binary-like manipulation(&|^~). Common usage is as follows:
>>> from Bio.Phylo.Consensus import _BitString >>> bitstr1 = _BitString('11111') >>> bitstr2 = _BitString('11100') >>> bitstr3 = _BitString('01101') >>> bitstr1 _BitString('11111') >>> bitstr2 & bitstr3 _BitString('01100') >>> bitstr2 | bitstr3 _BitString('11101') >>> bitstr2 ^ bitstr3 _BitString('10001') >>> bitstr2.index_one() [0, 1, 2] >>> bitstr3.index_one() [1, 2, 4] >>> bitstr3.index_zero() [0, 3] >>> bitstr1.contains(bitstr2) True >>> bitstr2.contains(bitstr3) False >>> bitstr2.independent(bitstr3) False >>> bitstr2.independent(bitstr4) True >>> bitstr1.iscompatible(bitstr2) True >>> bitstr2.iscompatible(bitstr3) False >>> bitstr2.iscompatible(bitstr4) True
In consensus and branch support algorithms, it is used to count and store the clades in multiple trees. During counting, the clades will be considered the same if their terminals(in terms of
name attribute) are the same.
For example, let's say two trees are provided as below to search their strict consensus tree:
tree1: (((A, B), C),(D, E)) tree2: ((A, (B, C)),(D, E))
For both trees, a
_BitString object '11111' will represent their root clade. Each '1' stands for the terminal clade in the list [A, B, C, D, E] (the order might not be the same, it's determined by the
get_terminal method of the first tree provided). For the clade ((A, B), C) in tree1 and (A, (B, C)) in tree2, they both can be represented by '11100'. Similarly, '11000' represents clade (A, B) in tree1, '01100' represents clade (B, C) in tree2, and '00011' represents clade (D, E) in both trees.
So, with the
_count_clades function in this module, finally we can get the clade counts and their _BitString representation as follows(the root and terminals are omitted):
clade _BitString count ABC '11100' 2 DE '00011' 2 AB '11000' 1 BC '01100' 1
To get the _BitString representation of a clade, we can use the following code snippet:
# suppose we are provided with a tree list, the first thing to do is # to get all the terminal names in the first tree term_names = [term.name for term in trees.get_terminals()] # for a specific clade in any of the tree, also get its terminal names clade_term_names = [term.name for term in clade.get_terminals()] # then create a boolean list boolvals = [name in clade_term_names for name in term_names] # create the string version and pass it to _BitString bitstr = _BitString(''.join(map(str, map(int, boolvals))))
To convert back:
# get all the terminal clades of the first tree terms = [term for term in trees.get_terminals()] # get the index of terminal clades in bitstr index_list = bitstr.index_one() # get all terminal clades by index clade_terms = [terms[i] for i in index_list] # create a new calde and append all the terminal clades new_clade = BaseTree.Clade() new_clade.clades.extend(clade_terms)
This is how the
_BitString is used in the consensus and branch support algorithms. And I think it can be used in many other conditions.
For example, we can even use it to check whether the structures of two trees are the same.
# store and return all _BitStrings def _bitstrs(tree): bitstrs = set() term_names = [term.name for term in tree.get_terminals()] term_names.sort() for clade in tree.get_nonterminals(): clade_term_names = [term.name for term in clade.get_terminals()] boolvals = [name in clade_term_names for name in term_names] bitstr = _BitString(''.join(map(str, map(int, boolvals)))) bitstrs.add(bitstr) return bitstrs def compare(tree1, tree2): term_names1 = [term.name for term in tree1.get_terminals()] term_names2 = [term.name for term in tree2.get_terminals()] # false if terminals are not the same if set(term_names1) != set(term_names2): return False # true if _BitStrings are the same if _bitstrs(tree1) == _bitstrs(tree2): return True else: return False
To use it:
>>> tree1 = Phylo.read('Tests/TreeConstruction/upgma.tre', 'newick') >>> tree2 = Phylo.read('Tests/TreeConstruction/nj.tre', 'newick') >>> tree3 = Phylo.read('Tests/TreeConstruction/pars1.tre', 'newick') >>> compare(tree1, tree2) False >>> compare(tree1, tree3) True >>> compare(tree2, tree3) False
- Bio.Phylo.PhymlCommandline provides a wrapper for PhyML following the usual Bio.Applications API.
- Bio.Phylo.PAML provides wrappers, parsers and utilities for working with the PAML suite of programs.
See the Biopython Tutorial sections on sequence alignment and BLAST for explanations of the first few steps shown here.
1. Search for homologs of a protein sequence using BLAST.
from Bio.Blast import NBCIStandalone, NCBIXML query_fname = 'AAG35789.fasta' result_handle, error_handle = NCBIStandalone.blastall('/usr/bin/blastall', 'blastp', '/db/fasta/swissprot', query_fname) blast_record = NCBIXML.read(result_handle) # This takes some time to run
2. Extract the best hits from the BLAST result.
from Bio import SeqIO from Bio.Seq import Seq from Bio.SeqRecord import SeqRecord def get_seqrecs(alignments, threshold): for aln in alignments: for hsp in aln.hsps: if hsp.expect < threshold: yield SeqRecord(Seq(hsp.sbjct), id=aln.accession) break best_seqs = get_seqrecs(blast_record.alignments, 1e-90) SeqIO.write(best_seqs, 'egfr-family.fasta', 'fasta')
To help with annotating to your tree later, pick a lookup key here (e.g. accession number) and build a dictionary mapping that key to any additional data you can glean from the BLAST output, such as taxonomy and GI numbers. In this example, we're only keeping the original sequence and accession number.
3. Re-align the sequences using Muscle. The program creates an alignment file in Clustal format, "egfr-family.aln".
from Bio.Align.Applications import MuscleCommandline cmdline = MuscleCommandline(input="egfr-family.fasta", out="efgr-family.aln", clw=True) cmdline()
4. Infer a gene tree using PhyML. First, convert the alignment from step 3 to "relaxed Phylip" format (new in Biopython 1.58):
from Bio import AlignIO AlignIO.convert("egfr-family.aln", "clustal", "egfr-family.phy", "phylip-relaxed")
Feed the alignment to PhyML using the command line wrapper:
from Bio.Phylo.Applications import PhymlCommandline cmdline = PhymlCommandline(input='egfr-family.phy', datatype='aa', model='WAG', alpha='e', bootstrap=100) out_log, err_log = cmdline()
5. Load the gene tree with Phylo, and take a quick look at the topology. (PhyML writes the tree to a file named after the input file plus "_phyml_tree.txt".)
from Bio import Phylo egfr_tree = Phylo.read("egfr-family.phy_phyml_tree.txt", "newick") Phylo.draw_ascii(egfr_tree)
6. Add accession numbers and sequences to the tree -- now we're using PhyloXML's extra features.
from Bio.Phylo import PhyloXML # Promote the basic tree to PhyloXML egfr_phy = egfr_tree.as_phyloxml() # Make a lookup table for sequences lookup = dict((rec.id, str(rec.seq)) for rec in best_seqs) for clade in egfr_phy.get_terminals(): key = clade.name accession = PhyloXML.Accession(key, 'NCBI') mol_seq = PhyloXML.MolSeq(lookup[key], is_aligned=True) sequence = PhyloXML.Sequence(type='aa', accession=accession, mol_seq=mol_seq) clade.sequences.append(sequence) # Save the annotated phyloXML file Phylo.write(egfr_phy, 'egfr-family-annotated.xml', 'phyloxml')