Man page - bali-phy(1)
Packages contains this manual
- alignment-consensus(1)
- cut-range(1)
- alignment-thin(1)
- alignment-max(1)
- bali-phy-pkg(1)
- bp-analyze(1)
- alignment-draw(1)
- summarize-ancestors(1)
- extract-ancestors(1)
- stats-select(1)
- mctree-mean-lengths(1)
- trees-consensus(1)
- alignment-find(1)
- bali-phy(1)
- statreport(1)
- alignment-indices(1)
- tree-mean-lengths(1)
- pickout(1)
- draw-tree(1)
- alignment-gild(1)
- alignment-distances(1)
- alignment-info(1)
- tree-tool(1)
- alignments-diff(1)
- trees-bootstrap(1)
- mcon-tool(1)
- alignment-cat(1)
- alignment-chop-internal(1)
- alignment-translate(1)
- trees-distances(1)
- bali-subsample(1)
apt-get install bali-phy
Manual
bali-phy
NAMESYNOPSIS
DESCRIPTION
GENERAL OPTIONS
MCMC OPTIONS
PARAMETER OPTIONS
MODEL OPTIONS
EXAMPLES
REPORTING BUGS
SEE ALSO
AUTHORS
NAME
bali-phy - Bayesian Inference of Alignment and Phylogeny
SYNOPSIS
bali-phy sequence-file1 [ sequence-file2 ...] [ OPTIONS ]
bali-phy help topic
DESCRIPTION
bali-phy estimates multiple sequence alignments and evolutionary trees from DNA, amino acid, or codon sequences. BAli-Phy uses MCMC and Bayesian methods to estimate evolutionary trees, positive selection, and branch lengths while averaging over alternative alignments.
BAli-Phy can also estimate phylogenies from a fixed alignment (like MrBayes and BEAST) using substitution models like GTR+gamma. BAli-Phy automatically estimates relative rates for each gene.
GENERAL OPTIONS
For each option
below, more information is available by specifying the long
form of the option as a help topic. For example: bali-phy
help alphabet
-h
,
âhelp
,
âhelp
=
topic
Display a friendly help message. Specify âhelp=advanced or âhelp=expert to display more advanced options.
-v , âversion
Print version information.
-V , âverbose , âverbose NUM
Print extra output to aid in trouble-shooting. If NUM is not specified the default is 1. Values from 2 to 4 increase the amount of information displayed.
-t , âtest
Analyze the initial values and exit.
-c filename , âconfig filename
Read commands from filename before command line.
MCMC OPTIONS
-i NUM , âiterations NUM
The number of iterations to run.
-n STRING , âname STRING
Name for the output directory to create.
-x NUM , âsubsample NUM
Factor by which to subsample. This option should usually not be used.
-s NUM , âseed NUM
Random seed. Useful for replaying specific runs when trouble-shooting.
-l arg , âlog-format arg
Log-format: tsv or json or tsv,json
PARAMETER OPTIONS
-T filename , âtree filename
File with initial tree in Newick format or NEXUS format.
-U , âunalign
Unalign all variable-alignment partitions before starting MCMC instead using the supplied alignment as a starting value.
MODEL OPTIONS
-A alphabet , âalphabet alphabet
The alphabet.
-S model , âsmodel model
The substitution model.
-I model , âimodel model
The insertion-deletion model.
-R arg , âscale arg
Prior on the scale.
-F arg , âfix arg
Fix topology, tree, or alignment
-L NUMS , âlink NUMS
Link partitions. Takes a comma-separated list of numbers indicating partitions. For example --link 1,2,3.
âvariables arg
Variable definitions
EXAMPLES
bali-phy dna.fasta --smodel gtr
Analyze sequences in dna.fasta under the GTR model.
bali-phy dna.fasta -S gtr -I none
Perform a traditional fixed-alignment analysis with gaps treated as missing data.
bali-phy dna.fasta amino.fasta
codons.fasta -S 1:gtr -S 2:lg08 -S
3:gy94
Perform an analysis of 3 genes where each gene has a different substitution mode. The sequence names in all three files must be the same.
REPORTING BUGS
BAli-Phy online help: http://www.bali-phy.org/docs.php .
Please send bug reports to bali-phy-users@googlegroups.com .
SEE ALSO
bp-analyze
AUTHORS
Benjamin Redelings.