On 25.01.2016 02:53, Michael Forthman wrote:
> I'm thinking it may be easier to run this on the desktop version of
> RAxML. However, I'm still confused as to how I can treat my partitions
> the way that I'm wanting to. I have to specify (-m), which only let's me
> specify one model. If I put GTRGAMMA, then this would be applied to each
> DNA and MULTI partition. But if I list MULTIGAMMA, would this apply the
> specified model in (-K) for MULTI partition but the GTRGAMMA model to
> DNA partitions (without estimating invariant sites)?
from the -m string only the model of rate heterogeneity will be
extracted, which is applied to all partitions (DNA and MULTI).
the value passed via -K then specifies which model will be applied to
the multi-state partition ...
> Also, I want to include ascertainment bias for the MULTI partition. Am I
> correct that I simply add ASC_ before MULTI in the partition file, and
> then in the command line -asc_corr=lewis if this is the correction I want?
yes, that should work.
> So far, this is how my command line is looking: raxmlHPC -f a -s
> CombinedMatrix.phy -x 2016 -p 4325 -n Result -m MULTIGAMMA -q
> partition.txt -asc_corr=lewis -K MK -o Peiratespunctorius -N 20
looks good,
alexis
>
> Cheers, Michael
>
> On Saturday, January 23, 2016 at 9:55:27 AM UTC-8, Michael Forthman wrote:
>
> Hello,
>
> I'm trying to run a ML analysis using CIPRES RAxML on a combined DNA
> and morphological (multi-state) dataset. I've posted to the CIPRES
> Google Groups, but was recommended to post here instead. I'm wanting
> to use a partition file (-q) and currently have it as such:
>
> DNA, p1 = 1-1024
> DNA, p2 = 1025-1855
> DNA, p3 = 1856-2628
> DNA, p4 = 2629-3054
> MULTI, morph = 3055-3199
>
> Here is the problem I am having trouble figuring out: I want to use
> a GTR+GAMMA+I for each of the four DNA partitions, but use the Lewis
> Mkv model (with asc correction) for the multi-state partition. Is
> there anyway I can specify this in the partition file? If I try
> selecting options in CIPRES that apply to the DNA partitions, I
> cannot select anything for the multi-state partitions, and vice versa.
>
> Cheers, Michael
>
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--
Alexandros (Alexis) Stamatakis
Research Group Leader, Heidelberg Institute for Theoretical Studies
Full Professor, Dept. of Informatics, Karlsruhe Institute of Technology
Adjunct Professor, Dept. of Ecology and Evolutionary Biology, University
of Arizona at Tucson
www.exelixis-lab.org