Closed Adelaam closed 5 years ago
please check your alignment, apparently it is not a valid FASTA file...
@Adelaam have you managed to fix the problem? if not, could you please post/e-mail your alignment and RAxML-NG command line?
is there any model for binary?
is there any updated manual for this version? Because this program making other models available.
@lixingguang please see here:
https://github.com/amkozlov/raxml-ng/wiki
https://github.com/amkozlov/raxml-ng/wiki/Input-data#evolutionary-model
@amkozlov, thanks. Could I know the detailed name for BIN model?
@lixingguang it's --model BIN
, please read the documentation...
@amkozlov , I know it is the command, I want to know the detail mode name?
With binary data, only one reversible substitution matrix is possible, since there is just one substitution rate 0 <-> 1
. This could however be combined with non-equal equilibrium state frequencies (BIN+FO
or BIN+F
).
Please read: https://en.wikipedia.org/wiki/Models_of_DNA_evolution or a standard textbook on computational phylogenetics (Felsenstein, Ziheng Yang...)
@lixingguang and @Adelaam: please use RAxML google group for asking questions about RAxML-NG:
https://groups.google.com/forum/#!forum/raxml
GitHub issues are better suited for bug reports and feature requests.
Thank you.
@amkozlov thanks. You are very kind. For google, it is not very easy for people in China to access, but still thanks again for all your help.
Hello Alexey,
Sorry for the late reply. Can I email you my alignment and command line?
From: Alexey Kozlov [mailto:notifications@github.com] Sent: 20 May 2019 18:03 To: amkozlov/raxml-ng Cc: Adelaam; Mention Subject: Re: [amkozlov/raxml-ng] --msa error (#68)
@Adelaamhttps://github.com/Adelaam have you managed to fix the problem? if not, could you please post/e-mail your alignment and RAxML-NG command line?
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@Adelaam yes. please e-mail them to me!
'/home/markwilks/raxml-ng_v0.8.1_linux_x86_64/raxml-ng' --msa '/home/markwilks/Desktop/Tree/52184072883polished.fasta' '/home/markwilks/Desktop/Tree/52184147961polised.fasta' '/home/markwilks/Desktop/Tree/52194095915polished.fasta' --model GTR+G
RAxML-NG v. 0.8.1 BETA released on 05.03.2019 by The Exelixis Lab. Authors: Alexey Kozlov, Alexandros Stamatakis, Diego Darriba, Tomas Flouri, Benoit Morel. Latest version: https://github.com/amkozlov/raxml-ng Questions/problems/suggestions? Please visit: https://groups.google.com/forum/#!forum/raxml
WARNING: This is a BETA release, please use at your own risk!
RAxML-NG was called at 28-May-2019 16:00:35 as follows:
/home/markwilks/raxml-ng_v0.8.1_linux_x86_64/raxml-ng --msa /home/markwilks/Desktop/Tree/52184072883polished.fasta /home/markwilks/Desktop/Tree/52184147961polised.fasta /home/markwilks/Desktop/Tree/52194095915polished.fasta --model GTR+G
Analysis options: run mode: ML tree search start tree(s): random (10) + parsimony (10) random seed: 1559055635 tip-inner: OFF pattern compression: ON per-rate scalers: OFF site repeats: ON fast spr radius: AUTO spr subtree cutoff: 1.000000 branch lengths: proportional (ML estimate, algorithm: NR-FAST) SIMD kernels: AVX parallelization: PTHREADS (2 threads), thread pinning: OFF
[00:00:00] Reading alignment from file: /home/markwilks/Desktop/Tree/52184072883polished.fasta
ERROR: Error loading MSA: cannot parse any format supported by RAxML-NG!
Please re-run with --msa-format
@Adelaam thanks for the files, the sequences in your FASTA file are not aligned, they have different lengths.
please use multiple sequence aligner before running raxml-ng!
Hi Alexey,
Thank you for your answer.
Maybe I did not understand it properly. I wat to see a tree with my sequences, which I assembled them the novo, than corrected and polished. Now I want to see the tree, I though you can put your sequences and then get the tree, but you say I need to align them, with what? With the reference one?
A
From: Alexey Kozlov [mailto:notifications@github.com] Sent: 28 May 2019 16:37 To: amkozlov/raxml-ng Cc: Adelaam; Mention Subject: Re: [amkozlov/raxml-ng] --msa error (#68)
@Adelaamhttps://github.com/Adelaam thanks for the files, the sequences in your FASTA file are not aligned, they have different lengths.
please use multiple sequence aligner before running raxml-ng!
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Hello,
I am trying to get tree with several polished.fasta sequences, and I am getting the next error: Error loading MSA: cannot parse any format supported by RAxML-NG! Please re-run with --msa-format and/or --log debug to get more information.
My sequences have several contigs starting cuch us >tig0001. How can I correct this error?
Thank you