MIGRATE(1) General Commands Manual MIGRATE(1) NAME MIGRATE - estimate population parameters: migration rate and population size SYNOPSIS migrate-n DESCRIPTION Migrate estimates population parameters (effective population size and mi- gration rates) using genetic data (Electrophoretic markers, microsatellite markers, sequence data, and single nucleotide polymorphism data). It is a maximum likelihood estimator or Bayesian estimator and uses a coalescent theory approach taking into account history of mutations and uncertainty of the genealogy. or get a copy of the manual in PDF format from http://popgen.scs.fsu.edu OPTIONS there are no options on the commandline, but you can specify the options in a parmfile or in the menu PARMFILE OPTIONS The parmfile options are split into Datatype, Input/Output, Start parame- ters, Search strategy DATATYPE datatype=<Allele | Microsatellites | Brownian | Sequences | Nucleotide- polymorphisms | Panel-SNP | Genealogies > specifies the datatype used for the analyses, needless to say that if you have the wrong data for the chosen type the program will crash. Allele: infinite allele model, suitable for electrophoretic markers, perhaps the "best" guess for codominant markers of which we do not know the mutation model. Microsatellite: a simple elec- trophoretic ladder model is used for the change along the branches in genealogy. Brownian: a Brownian motion approximation to the stepwise mutation model for microsatellites us used (this is MUCH faster than exact model, but is not a good approximation if popula- tion sizes are small (say below 10). Sequences: Data are DNA or RNA sequences and the mutation model used is F84, first used by Felsen- stein 1984 (actually the same as in dnaml (Phylip version 3.5), a description of this model can be found in Swofford et al. 1996. Nu- cleotide-polymorphism: [SNP] the data likelihood is corrected for sampling only variable sites. We assume that the data was used to find the SNP. Panel-SNP: the data likelihood is corrected for using a panel of SNP sites, that were polymorphic. The panel has to be population 1. Genealogies: Reads the sumfile of a previous run, with this options the genealogy sampling step will not be done and the genealogies provided in the sumfile are analyzed. This datatype makes it easy to rerun the program for different likelihood ratio test or different settings for the profile likelihood printouts. Sequence data specific options freq-from-data=< Yes | No:freqA freqG freqC freqT> ttratio=< r1 r2 .....> interleaved=<Yes | No > categories=<Yes | No> If you specify Yes you need a file named catfile in the same directory with the following Syntax: number_of_cate- gories cat1 cat2 cat3 .. categorylabel_for_each_site for each locus, a # in the first column can be used to start a comment-line. Exam- ple is for a data set with 2 loci and 20 base pairs each # Example catfile for two loci # in migrate you can use # as comments 2 1 10 11111111112222222222 5 0.1 2 5 23 3 11111122223333445555 rates=< n : r1 r2 r3 ..rn> prob-rates=< n : p1 p2 p3 ... pn> autocorrelation=<Yes:value | No> weights=<Yes | No> If you specify Yes you need a file weightfile with weights for each site, the weights can be the following numbers 0-9 and letters A-Z, so you have 35 possible weights available. # Example weightfile for two loci 11111111112222222222 1111112222AAAA445XXXX5 distfile=<Yes | No> You can supply a distance file for each locus (using PHYLIP syntax). The sequence of indiviudals must be same as in the infile. This op- tion appears in the menu when you choose 0 Start genealogy is estimated using a UPGMA topology The distance file is then used to create an UPGMA tree with a mini- mal number of migration events. For large trees this is options help to get better starting trees than the automatic tree generation which uses a rather unsophisticated distance method (differences). usertree=<Yes | No> If you specify Yes you need a file intree. In this file you have starting trees for each locus. BUT these trees need to have migra- tion events in them! Microsatellite data micro-threshold=value specifies the window in which probabilities of change are calculated if we have allele 34 then only probabilities of a change from 34 to 35-44 and 24-34 are considered, the higher this value is the longer you wait for your result, choosing it too small will produce wrong results. De- fault is micro-threshold=10 Electrophoretic data No special variables. Nucleotide polymorphism Similar to sequence data. INPUT/OUTPUT infile=filename Default is infile random-seed=<Auto | Noauto | Own:seedvalue> The random number seed guarantees that you can reproduce a run ex- actly. Good random number seeds are (values * 4) + 1. If you do not specify the random number seed ( seed=Auto ) the program will use the system clock. With seed=Noauto the program expects to find a file named seedfile with the random number seed. With random- seed=Own:seedvalue you can specify the seed value in the parmfile (or in the menu). title=titletext progress=<Yes|No|Verbose> The default is progress=Yes outfile=filename The default is obviously outfile=outfile print-data=<Yes|No> Print the data in the outfile. Default is print-data=No. print-fst=<Yes|No> Print a table of an FST estimate for comparison (Beerli and Felsen- stein 1999, Beerli 1998) [not recommended]. plot=<No | Yes>[:<Outfile|Both>[:<std|log>:{mig-axis-start,mig-axis- end,theta-axis-start,theta-axis-end}<:printpos<M | Nm>>]] If plot=No then no plot of the parameter space is shown in the out- file, if Yes then you can specify whether you want to have the accu- rate numbers in a separate file ( mathfile ) using printpos "pixel" in each direction,or only the ASCII-graphics plot in the outfile. The last option ( M or N )let you define whether you want the plot in M=m/mu or (default) 4Nm units. Default is plot=Yes:Out- file. Example of a more complicated statement: plot=Yes:Both:std:0,10,0,0.025:100N For syntax in mathfile see docu- mentation profile=<No|Yes<:<Fast|Percentile|Spline|Discrete|Quick >><:M | Nm > Print profile likelihood. See section Likelihood ratio tests and profile likelihood. Default is profile=Yes:Fast:N. l-ratio=<None | <Mean|Loci>:testparam> (N-POP) Likelihood ratio tests. See section Likelihood ratio tests and profile likelihood. Default is l-ratio=None. print-trees=<All | None | Last | Best> Default is print-trees=None mathfile=filename sumfile=<No | Yes | Yes:filename > Intermediate results of the genealogy sampling process are save into a file named sumfile or into the file for that you specify the file- name. You can use this sumfile to rerun the program for further analysis, e.g. calculating likelihood ratios or profile likeli- hoods, see datatype=Genealogy. START VALUES FOR THE PARAMETERS theta=<Fst | Own:{value1,value2 ,...}> With Fst the programs tries to use an FST based measure (Maynard Smith 1970, Nei and Feldman 1972) Own: { value1, value2, ... } defines arbitrary start values. migration=<Fst|Own:Migration matrix > (N-POP) The migration matrix is a n by n table with - on the diagonal and can look like this for four populations migration=OWN:{ - 1.0 1.1 1.2 0.9 - 0.8 0.7 2.1 2.2 - 2.3 1.4 1.5 1.6 - } or like this migration=OWN:{ - 1.0 1.1 1.2 0.9 - 0.8 0.7 2.1 2.2 - 2.3 1.4 1.5 1.6 - } mutation=<Gamma | NoGamma> The default is mutation=Nogamma fst-type=<Theta | Migration > custom-migration=< NONE|migration - matrix > The migration matrix contains the migration rates from j to i on row i, and the are on the diagonal. The migration matrix can consist of connections that are *: no restriction 0: not estimated m: mean value of either 4Nm or M. s: symmetric migration [only for M] c: constant value (together with migration=OWN.. or theta=OWN..) The values can be spaced by blanks, newlines. A few examples for 4 populations: Full model: custom-migration={**** **** **** ****} N-island model: custom-migration={m m m m mm mm m mmm mmmm} Stepping Stone model: with symmetric migrations, and unrestricted estimates: custom-migration={*s00 s*s0 0s*s 00s*} Source-Sink: (the first population is the source): custom-migra- tion={*000**000**0*000} SEARCH STRATEGY Please read the documentation ,these settings are important and will influ- ence the accuracy of your results. short-chains=value Default is 10. short-inc=value Default is 20. short-sample=value Default is 500. long-chains=value Default is 2. long-inc=value Default is 20. long-sample=value Default is 5000. burn-in=value Default is 10000. replicate=<NO | YES<:LONGCHAINS | number>> heating=<NO | YES<:{1,1.1,1.2,1.3}>> Obscure options see documentation BUGS This man page is not up to date and misses the Bayesian inference section, but see documentation. MAIN DISTRIBUTION WEBSITE http://popgen.csit.fsu.edu SEE ALSO coalesce, fluctuate, recombine, lamarc (the program) available from http://evolution.gs.washington.edu/lamarc.html AUTHOR Peter Beerli <beerli@csit.fsu.edu> [if you use this man page, please let me know] 4.2 Berkeley Distribution July 20 2006 MIGRATE(1)
NAME | SYNOPSIS | DESCRIPTION | OPTIONS | PARMFILE OPTIONS | DATATYPE | Sequence data specific options | Microsatellite data | Electrophoretic data | Nucleotide polymorphism | INPUT/OUTPUT | START VALUES FOR THE PARAMETERS | SEARCH STRATEGY | BUGS | MAIN DISTRIBUTION WEBSITE | SEE ALSO | AUTHOR
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