.\" Automatically generated by Pandoc 2.2.1 .\" .TH "bali\-phy" "1" "Feb 2018" "" "" .hy .SH NAME .PP bali\-phy \- Bayesian Alignment and Phylogeny estimation using MCMC .SH SYNOPSIS .PP \f[B]bali\-phy\f[] \f[I]sequence\-file1\f[] [\f[I]sequence\-file2\f[] \&...] [\f[I]OPTIONS\f[]] .PP \f[B]bali\-phy\f[] help \f[I]topic\f[] .SH DESCRIPTION .PP \f[B]bali\-phy\f[] 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. .PP 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. .SH GENERAL OPTIONS .PP 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 .TP .B \f[B]\-h\f[], \f[B]\-\-help\f[], \f[B]\-\-help\f[]=\f[I]topic\f[] Display a friendly help message. Specify \f[B]\-\-help=advanced\f[] or \f[B]\-\-help=expert\f[] to display more advanced options. .RS .RE .TP .B \f[B]\-v\f[], \f[B]\-\-version\f[] Print version information. .RS .RE .TP .B \f[B]\-t\f[], \f[B]\-\-test\f[] Analyze the initial values and exit. .RS .RE .TP .B \-V, \-\-verbose, \-\-verbose \f[I]NUM\f[] Print extra output to aid in trouble\-shooting. If \f[I]NUM\f[] is not specified the default is 1. Values from 2 to 4 increase the amount of information displayed. .RS .RE .TP .B \-c \f[I]filename\f[], \-\-config \f[I]filename\f[] Read commands from \f[I]filename\f[] before command line. .RS .RE .SH MCMC OPTIONS .TP .B \f[B]\-i\f[] \f[I]NUM\f[], \-\-iterations \f[I]NUM\f[] The number of iterations to run. .RS .RE .TP .B \-n \f[I]STRING\f[], \-\-name \f[I]STRING\f[] Name for the output directory to create. .RS .RE .TP .B \-x \f[I]NUM\f[], \-\-subsample \f[I]NUM\f[] Factor by which to subsample. This option should usually not be used. .RS .RE .TP .B \-s \f[I]NUM\f[], \-\-seed \f[I]NUM\f[] Random seed. Useful for replaying specific runs when trouble\-shooting. .RS .RE .SH PARAMETER OPTIONS .TP .B \-T \f[I]filename\f[], \-\-tree \f[I]filename\f[] File with initial tree in Newick format or NEXUS format. .RS .RE .TP .B \-U, \-\-unalign Unalign all variable\-alignment partitions before starting MCMC instead using the supplied alignment as a starting value. .RS .RE .SH MODEL OPTIONS .TP .B \-A \f[I]alphabet\f[], \-\-alphabet \f[I]alphabet\f[] The alphabet. .RS .RE .TP .B \-S \f[I]model\f[], \-\-smodel \f[I]model\f[] The substitution model. .RS .RE .TP .B \-I \f[I]model\f[], \-\-imodel \f[I]model\f[] The insertion\-deletion model. .RS .RE .TP .B \-B \f[I]prior\f[], \-\-branch\-lengths \f[I]prior\f[] Prior on branch lengths. .RS .RE .TP .B \-R \f[I]prior\f[], \-\-scale \f[I]prior\f[] Prior on the scale. .RS .RE .TP .B \-L \f[I]NUMS\f[], \-\-link \f[I]NUMS\f[] Link partitions. Takes a comma\-separated list of numbers indicating partitions. For example \f[B]\-\-link 1,2,3\f[]. .RS .RE .SH EXAMPLES .TP .B bali\-phy dna.fasta \-\-smodel gtr Analyze sequences in \f[I]dna.fasta\f[] under the GTR model. .RS .RE .TP .B bali\-phy dna.fasta \-S gtr \-I none Perform a traditional fixed\-alignment analysis with gaps treated as missing data. .RS .RE .TP .B 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. .RS .RE .SH REPORTING BUGS .PP BAli\-Phy online help: . .PP Please send bug reports to . .SH SEE ALSO .PP bp\-analyze .SH AUTHORS Benjamin Redelings.