.\" Automatically generated by Pandoc 2.17.1.1 .\" .\" Define V font for inline verbatim, using C font in formats .\" that render this, and otherwise B font. .ie "\f[CB]x\f[]"x" \{\ . ftr V B . ftr VI BI . ftr VB B . ftr VBI BI .\} .el \{\ . ftr V CR . ftr VI CI . ftr VB CB . ftr VBI CBI .\} .TH "bali-phy" "1" "Feb 2018" "" "" .hy .SH NAME .PP \f[B]bali-phy\f[R] - Bayesian Inference of Alignment and Phylogeny .SH SYNOPSIS .PP \f[B]bali-phy\f[R] \f[I]sequence-file1\f[R] [\f[I]sequence-file2\f[R] \&...] [\f[I]OPTIONS\f[R]] .PP \f[B]bali-phy\f[R] help \f[I]topic\f[R] .SH DESCRIPTION .PP \f[B]bali-phy\f[R] 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: \f[V]bali-phy help alphabet\f[R] .TP \f[B]-h\f[R], \f[B]--help\f[R], \f[B]--help\f[R]=\f[I]topic\f[R] Display a friendly help message. Specify \f[B]--help=advanced\f[R] or \f[B]--help=expert\f[R] to display more advanced options. .TP \f[B]-v\f[R], \f[B]--version\f[R] Print version information. .TP \f[B]-t\f[R], \f[B]--test\f[R] Analyze the initial values and exit. .TP \f[B]-V\f[R], \f[B]--verbose\f[R], \f[B]--verbose\f[R] \f[I]NUM\f[R] Print extra output to aid in trouble-shooting. If \f[I]NUM\f[R] is not specified the default is 1. Values from 2 to 4 increase the amount of information displayed. .TP \f[B]-c\f[R] \f[I]filename\f[R], \f[B]--config\f[R] \f[I]filename\f[R] Read commands from \f[I]filename\f[R] before command line. .SH MCMC OPTIONS .TP \f[B]-i\f[R] \f[I]NUM\f[R], \f[B]--iterations\f[R] \f[I]NUM\f[R] The number of iterations to run. .TP \f[B]-n\f[R] \f[I]STRING\f[R], \f[B]--name\f[R] \f[I]STRING\f[R] Name for the output directory to create. .TP \f[B]-x\f[R] \f[I]NUM\f[R], \f[B]--subsample\f[R] \f[I]NUM\f[R] Factor by which to subsample. This option should usually not be used. .TP \f[B]-s\f[R] \f[I]NUM\f[R], \f[B]--seed\f[R] \f[I]NUM\f[R] Random seed. Useful for replaying specific runs when trouble-shooting. .SH PARAMETER OPTIONS .TP \f[B]-T\f[R] \f[I]filename\f[R], \f[B]--tree\f[R] \f[I]filename\f[R] File with initial tree in Newick format or NEXUS format. .TP \f[B]-U\f[R], \f[B]--unalign\f[R] Unalign all variable-alignment partitions before starting MCMC instead using the supplied alignment as a starting value. .SH MODEL OPTIONS .TP \f[B]-A\f[R] \f[I]alphabet\f[R], \f[B]--alphabet\f[R] \f[I]alphabet\f[R] The alphabet. .TP \f[B]-S\f[R] \f[I]model\f[R], \f[B]--smodel\f[R] \f[I]model\f[R] The substitution model. .TP \f[B]-I\f[R] \f[I]model\f[R], \f[B]--imodel\f[R] \f[I]model\f[R] The insertion-deletion model. .TP \f[B]-B\f[R] \f[I]prior\f[R], \f[B]--branch-lengths\f[R] \f[I]prior\f[R] Prior on branch lengths. .TP \f[B]-R\f[R] \f[I]prior\f[R], \f[B]--scale\f[R] \f[I]prior\f[R] Prior on the scale. .TP \f[B]-L\f[R] \f[I]NUMS\f[R], \f[B]--link\f[R] \f[I]NUMS\f[R] Link partitions. Takes a comma-separated list of numbers indicating partitions. For example \f[V]--link 1,2,3\f[R]. .SH EXAMPLES .TP \f[V]bali-phy dna.fasta --smodel gtr\f[R] Analyze sequences in \f[I]dna.fasta\f[R] under the GTR model. .TP \f[V]bali-phy dna.fasta -S gtr -I none\f[R] Perform a traditional fixed-alignment analysis with gaps treated as missing data. .TP \f[V]bali-phy dna.fasta amino.fasta codons.fasta -S 1:gtr -S 2:lg08 -S 3:gy94\f[R] 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. .SH REPORTING BUGS .PP BAli-Phy online help: . .PP Please send bug reports to . .SH SEE ALSO .PP bp-analyze .SH AUTHORS Benjamin Redelings.