Dear all,
I recently faced the need to perform a phylogeographic analysis on several viral strains circulating across different European countries. In this context, my goal is both to identify significant state-to-state transition rates (i.e., migration links) and to assess potential predictors using a GLM framework.
Given the availability of several thousand sequences, I initially opted for a two-step approach to keep the analysis computationally tractable. First, I performed a phylodynamic analysis to estimate the tree distribution, and then Icalcualte the MCC tree to run the phylogeographic inference while keeping the topology fixed. To maintain consistency, I used BEAST X v10 for both steps, specifying operators appropriate for a fixed-topology analysis in the second run.
However, even under this setup, the phylogeographic analysis appears to proceed rather slowly and does not seem to reach convergence as quickly as expected. This was somewhat surprising, given that only a single fixed topology was used.
I was therefore wondering:
Any clarification or suggestions on hot to procced would be greatly appreciated.
Many thanks in advance.