Dear all,
I have performed genome wide dN/dS analysis of orthologs of six species.
Briefly, 1. orrthofinder for orthologs 2.pal2aln for codon-based alignment. 3.Codeml for dN/dS analysis.
in codeml file: I selected runmode=2, therefore I did not provide a user tree file.
After getting results, I saw there is no omega (dN/dS) value in the output file.
the output file has many best tree results, of all orthologs.
My question is how can I get omega value from the result file? and is it fine to select tree file from the output and use it in next codeml run as a "user tree file" ?
for selection the tree file; is it fine to use best tree that has highest log value?
Here is codeml file:
seqfile = all.paml * sequence data filename
outfile = mlc * main result file name
runmode = 2 * 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 = 2 * 0:1/61 each, 1:F1X4, 2:F3X4, 3:codon table
ndata = 5398 * number of gene alignments to be analysed
clock = 0 * 0:no clock, 1:clock; 2:local clock; 3:CombinedAnalysis
model = 0 * models for codons: 0:one, 1:b, 2:2 or more dN/dS ratios for branches
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
fix_omega = 0 * 1: omega or omega_1 fixed, 0: estimate
omega = .4 * initial or fixed omega, for codons or codon-based AAs
cleandata = 0 * remove sites with ambiguity data (1:yes, 0:no)?
- 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.
Thank you.