FastME: fast and accurate | ||
phylogeny reconstruction software |
PubMed | Entrez | BLAST | OMIM | Books | TaxBrowser | Structure |
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Downloads - the DOS executable version of FastME. - the C source code of FastME. - a small 9-taxon
data set that you can use to test the program. - the 3 trees that you
should obtain with DATATEST. References |
FastME is a fast phylogeny
reconstruction program based on the minimum evolution method. Among distance methods, FastME has shown better topological accuracy than Neighbor Joining,
BIONJ, WEIGHBOR and FITCH, in all evolutionary conditions we have tested,
including large range deviations from molecular clock and substitution rates.
When the number of taxa is high, its superiority over NJ, BIONJ and WEIGHBOR
becomes important, while FITCH remains close to FastME but becomes hard to use
due to its slowness. FastME is very fast, even faster than NJ, and can easily
be applied to very large data sets (> 1000 taxa). A PHYLIP compatible version can be downloaded from this web page. FastME was developed by Richard Desper (NCBI, Bethesda, USA) and Olivier Gascuel (LIRMM, Montpellier, France).
FastME first builds an
initial tree, using either GME or BME algorithms, and then improves this tree
by tree swapping, using either FASTNNI or BNNI algorithms. GME and FASTNNI
optimize the ordinary least-squares (OLS) version of the minimum-evolution
principle, while BME and BNNI optimize the balanced version. All simulations
indicate that the balanced version is much more appropriate. But the initial
tree has not much influence on the final tree that is obtained after tree
swapping. So the default options are GME (faster than BME) and BNNI (much more
accurate than FASTNNI). We suggest using these default options in all practical
situations, at least when using evolutionary distances estimated from
sequences. More explanations about the algorithms and their range of use are
given in the papers above. Distance matrices
must be in the square PHYLIP format. If the input file contains
several matrices given one after the other, as obtained when combining
SEQBOOT and DNADIST or PROTDIST to perform a bootstrap analysis,
FastME returns the same number of trees, written one after the other
in the output file; this file may be given to CONSENSE to obtain the
bootstrap tree.
FastME runs from a
MS-DOS or Unix window with the following options: -b specify
method for building initial tree: GME(default) or BME.
Not used if -t is used. -i filename
of distance matrix(ces). -n number of
matrices/trees (default = 1) -o filename
for tree output -s specify
type of tree swapping (NNI): (b)alanced, (O)LS, or (n)one. (default is
balanced.) -t
(optional) filename of starting tree topology -v provides the
progress of run (can be wrong with some systems) -help to get
the options For example, assuming that the datatest file (downloaded from this web page, see above) is in the C:\ directory, the line command:
fastme –i C:\datatest –n 3 –o C:\outputtree
will construct 3 trees
and write them (Newick format) into the file
Revised October 22, 2002 |