Difference between revisions of "SateTutorial"

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= Sate Tutorial =
 
= Sate Tutorial =
 
[http://phylo.bio.ku.edu/software/sate/sate.html Introduction and installation of SATE]
 
[http://phylo.bio.ku.edu/software/sate/sate.html Introduction and installation of SATE]

Latest revision as of 07:29, 7 October 2015


Sate Tutorial

Introduction and installation of SATE the installation guide shows how to run a commandline ommand and how to start the GUI, we will use the GUI for our "tutorial".

Tutorial

  1. start the GUI
  2. load a dataset from the example data (for example simple.fasta) and then try to run it, it will generate an alignment and a tree, try to look at the tree (for example use the program figtree)
  3. Explore the options using the text below.

SATE Overview

(this is a reformatted document from the README in the doc folder of the sate distribution) Sate website at Mark Holder's lab

SATe is a tool for producing trees and alignments from unaligned sequence data. It iterates between alignment and tree estimation, so that each iteration creates an alignment using a divide-and-conquer strategy of the maximum likelihood (ML) tree from the ML tree obtained in the previous iteration, and then computes a new ML tree on the new alignment.

The original algorithmic approach is described in:

Kevin Liu, Sindhu Raghavan, Serita Nelesen, C. Randal Linder, and  Tandy
Warnow. "Rapid and Accurate Large-Scale Coestimation of Sequence Alignments
and Phylogenetic Trees" Science. 2009. Vol. 324(5934), pp. 1561- 1564.
DOI: 10.1126/science.1171243

The algorithmic approach used in the current software is described in:

Kevin Liu, Tandy Warnow, Mark T. Holder, Serita Nelesen, Jiaye Yu, Alexis
Stamatakis, and C. Randal Linder. "SATe-II: Very Fast and Accurate
Simultaneous Estimation of Multiple Sequence Alignments and Phylogenetic
Trees."  Systematic Biology, 61(1):90-106, 2011.

The SATe software is written by Jiaye Yu, Mark T. Holder, Jeet Sukumaran, Siavash Mirarab, and Jamie Oaks, and uses the Dendropy library of Sukumaran and Holder.

Caveats

SATe software is currently available for testing purposes.

Please check your results carefully, and contact us if you have questions, suggestions or other feedback.

We are aware that the error-reporting needs work. If the software fails to produce output files despite the fact it announces that it is finished, then an error has occurred. We are working on having SATe give useful error messages. In the meantime, please contact us for help if you experience problems running SATe.

Temporary files: SATe uses a .sate directory in your HOME directory to store temporary results. In general the GUI tries to clean up after itself, but you may want to check that location if you think that SATe has been using too much hard disk space.

Graphical user interface version

The graphical user interface (GUI) for SATe gives you access to most of the available options for running the software. Below are brief descriptions of the settings that you can control via the GUI.

Starting conditions

If you give SATe a starting tree, it will go directly to the iterative portion of the algorithm.

If you do NOT give it a starting tree, then SATe will use the specified "Tree estimator" external tool to infer the initial tree. This requires an alignment, and you can provide an alignment as input to SATe. If you do not provide an alignment, then SATe will use the alignment tool that you have selected to produce an initial alignment for the entire dataset (this can be slow).

If the initial alignment is very slow, you might want to use the PartTree tool in MAFFT http://bioinformatics.oxfordjournals.org/content/23/3/372.abstract to estimate a rough starting tree. By providing SATe with the tree estimated by PartTree, your analysis will bypass the initial alignment/tree-search, and will immediately begin the first iteration of the SATe algorithm.

Soon, we will implement an option that allows you to specify an aligner for
the initial alignment operation and a different aligner for the subproblem
alignment operations. In the meantime, if you want a "quick and dirty"
alignment for the initial tree searching, you will need to produce this
alignment yourself and then give it to SATe.

External Tools (upper left)

During each iteration SATe breaks down the tree into subproblems, realigns the data for each subset, merges the alignments into a full alignment, and re-estimates the tree for the full alignment.

In the external tools section of the application you can choose the software tools used for each step:

* "Aligner" is used to select the multiple sequence alignment tool used to
  produce the initial full alignment (this can be slow!), and to align the
  subproblems.

* "Merger" is used to select the multiple sequence alignment tool used to
  merge the alignments of subproblems into a larger alignment.

* "Tree Estimator" will allow you to choose the software for tree inference
  from a fixed alignment.

* "Model" allows you to select the substitution model that will be used
  by the tree estimator during tree inference. The options in the drop down
  are contingent on the specified "Tree Estimator".

Sequences and Tree (middle left)

* If you are running a single locus analysis, leave the "Multi-Locus Data"
  box unchecked. Check this box if you want to run SATe with multiple loci.
  In multi-locus mode, during each iteration SATe aligns each locus
  separately, and then concatenates the alignments for a multi-locus tree
  search.

* If "Multi-Locus Data" is unchecked, clicking the "Sequence file..." button
  will allow you to select the input sequences in a FASTA-formatted file. If
  "Multi-locus Data" is checked, clicking the "Sequence file..." button will
  allow you to select the directory where the fasta files for each locus are
  located.
  
* NOTE: In multi-locus mode SATe will process ONLY files in the designated
  directory that end in ".fas" or ".fasta", and will treat each as a
  separate locus. All other files and directories will be ignored.

* NOTE: SATe version 2.2.0 or later automatically determines good
  analysis settings based on the size of the dataset(s) read with the
  "Sequence file..." button.  Thus, it is best to READ YOUR DATA FIRST,
  before setting other options, because settings will change when you read
  in your data.  It is still encouraged that you explore settings, but this
  new feature will provide a good starting point based on the amount of
  data.

* Clicking the "Tree file (optional)..." button will allow you to select a
  file with a NEWICK (Phylip) representation of the tree.  If you give SATe
  a starting tree, then it will not align the full dataset before the first
  iteration. Because the initial alignment of the full dataset can be quite
  slow, specifying a starting tree can dramatically reduce the running time.

* Use the "Data type" drop down menu to specify whether the data should be
  treated as DNA, RNA, or amino acid sequences (because of the 15 IUPAC
  codes for ambiguous states for DNA, it can be difficult to detect the
  datatype with absolute certainty).

Workflow Settings (lower left)

* Checking the "Two-Phase" algorithm will cause SATe to only perform an
  initial alignment and tree search and return the results.  It will NOT
  perform the SATe decomposition-merge algorithm.  This is the same as
  running the "Aligner" and "Tree Estimator" on your own.
  
* Checking the "Extra RAxML Search" post-processing option will cause SATe
  to perform a final RAxML search on the alignment returned by the SATe
  algorithm. This only makes sense if you are using a "Tree Estimator" other
  than RAxML.

Job Settings (upper right)

* "Job Name" allows you to specify the prefix for all files output by SATe.
  Files tagged with this name will appear in the output directory when the
  run completes.

* Clicking the "Output Dir." button will allow you to choose the output
  directory to which to save the alignments and trees returned by SATe. If
  you leave this blank, by default, the results will be written to the same
  directory as the source data file(s).

* "CPU(s) Available" allows you to specify how many processors should be
  dedicated to the alignment tasks of SATe. If you have a dual-core machine,
  then choosing 2 should decrease the running time of SATe because
  subproblem alignments will be conducted in parallel. In general, for the
  fastest performance, set this equal to the number processors in your
  machine.

* "Max. Memory (MB)" lets you specify the size of the Java Virtual Machine
  (JVM) heap to be allocated when running Java tools such as Opal. This
  should be as large as possible. If you get errors when running Java tools,
  one possible reason might be that you have allocated insufficient memory
  to the JVM given the size of your dataset. By default, the memory defaults
  to 1024 MB (versions of SATe prior to 2.0.3 had a default of 2048 MB, and
  did not allow the option of changing this).

SATe Settings (lower right)

The options in this panel allow you to control the details of the algorithm.

During each iteration, the dataset will be decomposed into non-overlapping subsets of sequences, and then these subproblems are given to the alignment tool that you have chosen.

* The "Max. Subproblem" settings control the largest dataset that will be
  aligned during the iterative part of the algorithm.  Use the "Fraction"
  button and the associated drop-down menu if you would like to express the
  maximum problem size as a percentage of the total number of taxa in the
  full dataset (e.g. 20 for "20%").

* If you want to express the size cutoff in absolute number of sequences,
  use the "Size" button and its drop-down menu.

* "Decomposition" allows you to select the procedure used to find the edge
  that should be broken to create subproblems.

* The "Stopping Rule" section allows you to control how SATe decides that it
  is done. The decision to stop the run can be done based on the number of
  iterations ("Iteration Limit" settings) or the amount of time in hours
  (the "Time Limit (hr)" settings).

* If you choose "Blind Mode Enabled", SATe will accept tree/alignment
  proposals even if they do not improve the ML score. If the "blind" mode is
  not in effect, then only pairs with a higher ML score will be accepted.
  
* The "Apply Stop Rule" drop down allows you to designate when the stopping
  should be applied or reset.  When you are running in "blind" mode, you can
  elect to have the stopping rule count the number of iterations (or the
  time) over the entire run ("After Launch"), or you can use a termination
  condition that is based on the progress since the last improvement in ML
  score ("After Last Improvement"). For example, if you choose "Blind Mode
  Enabled", an "Iteration Limit" of 1, and "After Last Improvement", then
  SATe will terminate if it even completes one iteration without improving
  the ML score. The effect of this will be that SATe iterations act like a
  strictly uphill climber in terms of the ML score.

* The "Return" drop down allows you to designate whether the tree (and 
  corresponding alignment) returned is the one with the "Best" ML score,
  or the one from the last or "Final" SATe iteration.


Notes for Developers

Putting: SATE_DEVELOPER=1 in your environment will display full stack traces on error exits.

Putting: SATE_LOGGING_LEVEL=debug in your environment will display debugging level logged messages

Putting: SATELIB_TESTING_LEVEL=EXHAUSTIVE will cause more tests to be executed when you run: $ python setup.py test

Acknowledgments

Code for OptionParsing was taken from Tim Chase's post on: http://groups.google.com/group/comp.lang.python/msg/09f28e26af0699b1