Closed mirix closed 4 years ago
Hi @mirix,
two weeks sounds like a bit too long even for 5000 seqs. Could you please post your log file?
If you need a "quick and dirty" tre, you can use parsimony (--start --tree pars{1}
), or ML tree from a single starting tree (eg --search1
or --search --tree pars{1}
).
Best, Alexey
Well, you are using a wrong model name:
ERROR: ERROR model initialization |PROT| (LIBPLL-5002): Invalid rates symmetry definition:
Please find a list of available protein models here: https://github.com/amkozlov/raxml-ng/wiki/Input-data#single-model
Sorry, I had overwritten the original log file...
That was the command line:
raxml-ng --msa PDBBind_ali.fasta --model LG --prefix T3 --threads 6 --seed 2
ok this looks better :)
but could you please post complete log file with the correct model?
@mirix closing since I never got a correct log file form you. Please reopen if you are still interested in this one.
Hello,
I have an alignment of highly divergent protein sequences with some 5000 sequences. I would like to derive a quick and dirty phylogenetic tree.
Online servers do not accept that many sequences whereas parallel codes such as RAXML-NG and IQ-TREE take for ever (over two weeks and counting) on a Xeon hexacore at 3.6 GHz. Whereas others require more than the 16GB of RAM I have.
Is it possible to derive a quick and dirty tree with RAXML-NG? If so, what the command line would be? How long should I expect it to take?
Best,
Miro