Another quick question.
I was running a test on 10 bird taxa (individual mt DNA region spread over several individuals from several families), with two calibration points from previous studies, and running two replicates of each. Getting good ess values well above 200 due to 10 mil + runs and after burnin runs look good BUT when comparing two runs in Tracer I seem to be getting bimodality BETWEEN them (not within each run) in several factors (namely proportion invariant, ucldST DEV, rate Coef of Variation). Another poster (Remco) explained that this meant non-convergence and suggested using bModelTest. Having read the PDF and done the tutorial (with primate mtDNA dataset) I have several questions regarding this program and settings:-
1. Am I correct in my understanding that bModelTest can be used to select the most appropriate model for the dataset AND to find the correct consensus tree at the same time i.e. alleviating the need to specify the substitution model (i.e. HKY, GTR etc) as you would normally do?
2. Also I am assuming that you also have burn-in periods when using bModelTest, is this correct?
3. Is there any reason that I cannot use my two calibration sets (set-up in prior section) in bModelTest AND if OK is there any specific settings I should be aware of?
4. Regarding settings, as my data is mtDNA I have partitioned each region dataset on codon position (C1/2/3) and run these unlinked BUT have linked their clock model and tree model, reasoning that as each region (the whole mitogenome in fact) is a single gene in time and so should be linked...is this correct?
5. As my dataset in not intraspecific I am correct to use a relaxed clock log normal model rather than a strict clock model?...I originally chose the relaxed clock log normal model rather than the relaxed clock exponential model as I read in the literature that it was most appropriate BUT would the exponential model be more appropriate and if so can someone explain why?
6. Finally, am I best leaving the rest of the priors at the default settings OR should I tweak specific ones (and which).
Sorry for so many questions but hopefully (or hopefully not) someone else is going through a similar scenario and this will help them at the same time.Thanks for you comments/help.
Edward
On 23/07/2018, at 5:35 AM, Edward B <egb...@gmail.com> wrote:1. Am I correct in my understanding that bModelTest can be used to select the most appropriate model for the dataset AND to find the correct consensus tree at the same time i.e. alleviating the need to specify the substitution model (i.e. HKY, GTR etc) as you would normally do?
2. Also I am assuming that you also have burn-in periods when using bModelTest, is this correct?
3. Is there any reason that I cannot use my two calibration sets (set-up in prior section) in bModelTest AND if OK is there any specific settings I should be aware of?
4. Regarding settings, as my data is mtDNA I have partitioned each region dataset on codon position (C1/2/3) and run these unlinked BUT have linked their clock model and tree model, reasoning that as each region (the whole mitogenome in fact) is a single gene in time and so should be linked...is this correct?
5. As my dataset in not intraspecific I am correct to use a relaxed clock log normal model rather than a strict clock model?...I originally chose the relaxed clock log normal model rather than the relaxed clock exponential model as I read in the literature that it was most appropriate BUT would the exponential model be more appropriate and if so can someone explain why?
6. Finally, am I best leaving the rest of the priors at the default settings OR should I tweak specific ones (and which).