I have a dataset with 762bp (254aa) of exon sequences from a single gene for 7 species. I would like to use CodeML to estimate the fit of a model of one omega across the entire tree v. varying omegas on different branches (M0 v M1 or 2). I was hoping obtain likelihood values for runs using the alternate models in CodeML so that I could perform a likelihood ratio test. However, I can't seem to find the likelihood in the output file. I am still stuck on the first step of running CodeML with the M0 model. I should note that I am also unable to find a tree-wide omega average in the output files.
I thought the problem might be that I had verbose = 0 and thus was not getting all the information in the output. However, when I change verbose to either 1 or 2, I get a segmentation fault. I should note that output files are still produced, and contain the same information as the output files obtained running CodeML with verbose=0.
So, I am not sure if there is a problem with my input data, my control file, or if there is a memory allocation issue.
Any suggestions? I have tried changing many things, but the pattern is the same. I will paste in my control file below.
seqfile = reduced_taxa_rat.phy
treefile = reduced_treefile
outfile = reduced_rat_outfile * main result file name
noisy = 9 * 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 = 1 * 1:codons; 2:AAs; 3:codons-->AAs
CodonFreq = 0
model = 0
NSsites = 0
icode = 0 * 0:universal code; 1:mammalian mt; 2-10:see below
clock = 0 * 0:no clock, 1:global clock; 2:local clock
fix_kappa = 0 * 1: kappa fixed, 0: kappa to be estimated
kappa = 10 * initial or fixed kappa
fix_omega = 0 * 1: fix omega at omega (below), 0: estimate omega
omega = 0.1 * initial or fixed omega, for codons or codon-based AAs
fix_alpha = 1 * 0: estimate gamma shape parameter; 1: fix it at alpha
alpha = 0. * initial or fixed alpha, 0:infinity (constant rate)
Malpha = 0 * different alphas for genes
ncatG = 0 * # of categories in dG of NSsites models
getSE = 1 * 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 = 1e-6
* cleandata = 0 * remove sites with ambiguity data (1:yes, 0:no)?
method = 0 * 0: simultaneous; 1: one branch at a time
fix_blength = 0 * 0: ignore, -1: random, 1: initial, 2: fixed