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uninstall any existing version of Spectronet before
installing this version.
This new version of Spectronet includes Closest
Tree and cluster-powered Fast Hadamard Transform
algorithms, the Treeness Triangle for visualising
sequence information, and several bug fixes. Consult
the in-program help for more information on the
new features. |
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Updated
6/12/2004 |
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This
program implements the methods described in
Holland,
B. R., K.T. Huber, D. Penny, and V. Moulton.
2005. The MinMax Squeeze: Guaranteeing
a minimal tree for
population data. Mol. Biol. Evol. 22:235-242.
and
Pierson, M.J., R. Martinez-Arias,
B.R. Holland, N.J. Gemmell, M.E. Hurles, and
D. Penny. 2006. Deciphering
Past
Human Population Movements in Oceania: Provably
Optimal Trees of 127 mtDNA Genomes. Mol.
Biol. Evol. 23(10).
for
finding lower bounds on the parsimony score
of an alignment. |
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Updated
12/8/2006 |
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Two-States Triplet Markov — 2STM
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calculates Markov matrices from 2-state character
data sets with 3 sequences simultaneously. The
program reads 4-state character nucleotide data
sets and outputs estimates of the three Markov
matrices from the root to each taxon. 2STM also
calculates the variability of estimates (bootstrap)
and some simple statistics, such as composition
of nucleotide characters, either in 4 states
or 2 states.
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Executable Windows program,
C code and example data can be
obtained from this
WinZip file.
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Contact Details
Michael Woodhams
Allan Wilson Centre
Institute of Molecular
BioSciences PN462
Massey University
Palmerston North,
New Zealand
Phone: +64
6 356 9099
ext 2570
E-mail
m.d.woodhams@massey.ac.nz
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Version
1.0, November 2002 | Michael Woodhams |
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Site Strip Search
— For site-stripping analyses of nucleotide alignments.
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This script selects subsets of taxa from a given alignment. The subsets are
chosen arcording to the homoplasy of the sites. The resulting data set may
be automatically sent to PAUP* or MrBayes for further analysis.
This beta version has been
tested on Linux and Windows operating systems.
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The Perl script can be down- loaded as a
zip or
gzip archive.
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Contact Details
Warwick Allen
Allan Wilson Centre
Institute of Molecular
BioSciences PN462
Massey University
Palmerston North,
New Zealand
Phone: +64
6 356 9099
ext 5449
E-mail
w.p.allen@massey.ac.nz
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Version
β0.2, January 2007 | Warwick Allen |
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Quartet-Imputation Supernetworks |
This program implements the methods described in
Holland, B. R., G. Conner, K. Huber, V. Moulton. 2006. Imputing supertrees and supernetworks from quartets. Systematic Biology (to appear).
and
Holland, B. R., G. Conner, K. T. Huber, V. Moulton. 2006. Imputing supertrees and supernetworks from quartets, (1 page abstract). In: 6th Workshop on Algorithms in Bioinformatics (WABI 2006) Eds B. Moret and P. Buchner, Lecture Notes in Bioinformatics. 4175:162.
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Contact Details
Barbara Holland
Allan Wilson Centre
Institute of Molecular
BioSciences PN462
Massey University
Palmerston North,
New Zealand
Phone: +64 6 356 9099
ext 7939
E-mail
b.r.holland@massey.ac.nz
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Version 1.0, February 2006 |
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Genotyping Utilities Package
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GenoTyper Rearranger (GTR) is a utility that converts the output AFLP data from genotyping programs (currently ABI's GeneMapper and SoftGenetics' GeneMarker) to various formats, allowing easier display and manipulation.
AFLP Replicate Difference Calculator is a utility calculates the difference of some parameter (peak height, for example) between replicates in a table of AFLP data. This script takes two inputs: the AFLP data and a table that declares which samples are replicates of which other samples.
See the AFLP page for more details.
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Contact Details
Warwick Allen
Allan Wilson Centre
Institute of Molecular
BioSciences PN462
Massey University
Palmerston North,
New Zealand
Phone: +64 6 356 9099
ext 5449
E-mail
w.p.allen@massey.ac.nz
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Version 1.1, May 2006 |
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LineageSpecificSeqgen is an extension to the seq-gen program that
allows generation of sequences with both changes
in the proportion of variable sites and changes
in the rate at which sites switch between being
variable and invariable.
Ref:
Shavit L, Penny D, Hendy MD, Holland BR: LineageSpecificSeqgen:
generating sequence data with lineage-specific
variation in the proportion of variable sites.
BMC Evolutionary Biology 2008 (in press).
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Updated
12/8/2006 |
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