/cons_test/ctl/codeml_aa.ctl
http://github.com/sbotond/phylosim · Visual Basic · 58 lines · 47 code · 11 blank · 0 comment · 6 complexity · e287ec4bd42a9b6dc3d06957c51836ae MD5 · raw file
- seqfile = sim.phy * sequence data filename
- treefile = ../tree/test_tree.t * tree structure file name
- outfile = mlc * main result file name
-
- noisy = 0 * 0,1,2,3,9: how much rubbish on the screen
- verbose = 1 * 0: concise; 1: detailed, 2: too much
- runmode = 0 * 0: user tree; 1: semi-automatic; 2: automatic
- * 3: StepwiseAddition; (4,5):PerturbationNNI; -2: pairwise
-
- seqtype = 2 * 1:codons; 2:AAs; 3:codons-->AAs
- CodonFreq = 2 * 0:1/61 each, 1:F1X4, 2:F3X4, 3:codon table
-
- * ndata = 10
- clock = 0 * 0:no clock, 1:clock; 2:local clock; 3:CombinedAnalysis
- aaDist = 0 * 0:equal, +:geometric; -:linear, 1-6:G1974,Miyata,c,p,v,a
- aaRatefile = ../ctl/wag.dat * only used for aa seqs with model=empirical(_F)
- * dayhoff.dat, jones.dat, wag.dat, mtmam.dat, or your own
-
- model = 3
- * models for codons:
- * 0:one, 1:b, 2:2 or more dN/dS ratios for branches
- * models for AAs or codon-translated AAs:
- * 0:poisson, 1:proportional, 2:Empirical, 3:Empirical+F
- * 6:FromCodon, 7:AAClasses, 8:REVaa_0, 9:REVaa(nr=189)
-
- NSsites = 0 * 0:one w;1:neutral;2:selection; 3:discrete;4:freqs;
- * 5:gamma;6:2gamma;7:beta;8:beta&w;9:betaγ
- * 10:beta&gamma+1; 11:beta&normal>1; 12:0&2normal>1;
- * 13:3normal>0
-
- icode = 0 * 0:universal code; 1:mammalian mt; 2-10:see below
- Mgene = 0
- * codon: 0:rates, 1:separate; 2:diff pi, 3:diff kapa, 4:all diff
- * AA: 0:rates, 1:separate
-
- fix_kappa = 0 * 1: kappa fixed, 0: kappa to be estimated
- kappa = 2 * initial or fixed kappa
- fix_omega = 0 * 1: omega or omega_1 fixed, 0: estimate
- omega = .4 * initial or fixed omega, for codons or codon-based AAs
-
- fix_alpha = 0 * 0: estimate gamma shape parameter; 1: fix it at alpha
- alpha = 1 * initial or fixed alpha, 0:infinity (constant rate)
- Malpha = 0 * different alphas for genes
- ncatG = 8 * # of categories in dG of NSsites models
-
- getSE = 0 * 0: don't want them, 1: want S.E.s of estimates
- RateAncestor = 0 * (0,1,2): rates (alpha>0) or ancestral states (1 or 2)
-
- Small_Diff = .5e-6
- cleandata = 1 * remove sites with ambiguity data (1:yes, 0:no)?
- * fix_blength = -1 * 0: ignore, -1: random, 1: initial, 2: fixed
- method = 0 * Optimization method 0: simultaneous; 1: one branch a time
-
- * Genetic codes: 0:universal, 1:mammalian mt., 2:yeast mt., 3:mold mt.,
- * 4: invertebrate mt., 5: ciliate nuclear, 6: echinoderm mt.,
- * 7: euplotid mt., 8: alternative yeast nu. 9: ascidian mt.,
- * 10: blepharisma nu.
- * These codes correspond to transl_table 1 to 11 of GENEBANK.