your partition file looks good.
please post FULL output of raxml-ng
On 13.11.24 07:59, Sithions Brand wrote:
> Dear Prof Kozlov,
>
> You're absolutely right about your suggestion, and I appreciate it. However, isn't it true that
> **RAxML-NG** doesn't support specifying codon partition models? Because in my **PartitionFinder**
> file, as shown in the image, I get an error during runtime saying the model cannot be found.
>
>
> my partitionfinder.txt:
> GTR+G, Subset1 = 1-976, 977-2568
> TrN+I+G, Subset2 = 12604-13965\3, 2569-3249\3
> TVM+I, Subset3 = 2570-3249\3, 12264-12603\3
> HKY+G, Subset4 = 2571-3249\3, 3250-3411\3
> TrN+I, Subset5 = 3251-3411\3
> GTR+G, Subset6 = 4965-5651\3, 5654-6435\3, 10248-11232\3, 3252-3411\3, 12606-13965\3, 14265-16071\3
> TIM1+I, Subset7 = 3412-4962\3
> TPM1uf, Subset8 = 3413-4962\3
> TrN, Subset9 = 3414-4962\3
>
> So I get an ERROR: ERROR model initialization |partition.txt| (LIBPLL-5001): DNA model not found:
> partition.txt
>
> Best wishes
>
> Brand
>
https://github.com/amkozlov/raxml-ng/wiki/Input-data#multiple-models <
https://github.com/
> amkozlov/raxml-ng/wiki/Input-data#multiple-models>
>
> Best,
> Oleksiy
>
> On 12.11.24 15:54, Sithions Brand wrote:
> > Hi evevyone,
> >
> > RAxML allows for only a single model of rate heterogeneity in partitioned analyses. I.e. all
> > partitions must be assigned one of three types of model: No heterogeneity (e.g. GTR); +G (e.g.
> > GTR+G); or +I+G (e.g. GTR+I+G).
> >
> > If my mitochondrial sequence partitions each have different models, such as GTR+G, HKY+G,
> JC+G, and
> > K80+I+G, how should I set the model parameters in RAxML?
> >
> > Best wishes
> >
> > Sithions Brand
> >
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