I'm really looking forward to hearing these 21 exciting presentations (and additional 30 posters) next December.
If you want to attend too, registration is open until October 17th through legend2025.sciencesconf.org
I'm really looking forward to hearing these 21 exciting presentations (and additional 30 posters) next December.
If you want to attend too, registration is open until October 17th through legend2025.sciencesconf.org
Mark your calendars and make sure your best work is ready next September when the call for abstracts opens 🙂
legend2025.sciencesconf.org
Mark your calendars and make sure your best work is ready next September when the call for abstracts opens 🙂
legend2025.sciencesconf.org
@lblassel.bsky.social , assisted by P. Veber, Bastien Boussau
and myself.
The code and data are available at github.com/lucanest/Phy...
Please share if you find this interesting, and we welcome your feedback :)
@lblassel.bsky.social , assisted by P. Veber, Bastien Boussau
and myself.
The code and data are available at github.com/lucanest/Phy...
Please share if you find this interesting, and we welcome your feedback :)
About two orders of magnitude faster than IQtree, and even twice faster than FastME.
About two orders of magnitude faster than IQtree, and even twice faster than FastME.
It outperformed all other methods, including IQTree/FastTree, on all metrics.
It outperformed all other methods, including IQTree/FastTree, on all metrics.
Looking at the topology only (Robinson-Foulds metric), it performed less well than IQTree/FastTree, but better than FastME.
Looking at the topology only (Robinson-Foulds metric), it performed less well than IQTree/FastTree, but better than FastME.
It performed much better than FastME (distance method), on par with maximum likelihood approaches (IQTree, FastTree).
It performed much better than FastME (distance method), on par with maximum likelihood approaches (IQTree, FastTree).
This choice makes our function invariant to the order of the input sequences (any order yields the same output phylogeny).
This choice makes our function invariant to the order of the input sequences (any order yields the same output phylogeny).
But each of these distance estimates is informed by the entire set of sequence, not just the corresponding pair!
We then pass them to FastME, a distance method, to obtain a tree.
But each of these distance estimates is informed by the entire set of sequence, not just the corresponding pair!
We then pass them to FastME, a distance method, to obtain a tree.
We optimize this function on a large number of (phylogeny, sequences) sampled from the probabilistic model.
We optimize this function on a large number of (phylogeny, sequences) sampled from the probabilistic model.
Sampling trees and sequences under a probabilistic model is possible under much more complex models, for which likelihood computations would be prohibitive.
It's an alternative way to access the model.
Sampling trees and sequences under a probabilistic model is possible under much more complex models, for which likelihood computations would be prohibitive.
It's an alternative way to access the model.
This makes them accurate but slow. It also restricts these approaches to simplistic models under which likelihood computations are fast enough.
This makes them accurate but slow. It also restricts these approaches to simplistic models under which likelihood computations are fast enough.
Distance methods rely on this idea, with estimates from pairs of sequences taken separately. This makes them fast but inaccurate.
Distance methods rely on this idea, with estimates from pairs of sequences taken separately. This makes them fast but inaccurate.
In probabilistic models, branch lengths represent an expected number of substitutions between the sequences at the two ends.
In probabilistic models, branch lengths represent an expected number of substitutions between the sequences at the two ends.
Faster than distance methods like neighbor joining, it outperforms maximum likelihood methods under complex models of sequence evolution.
🧵
Faster than distance methods like neighbor joining, it outperforms maximum likelihood methods under complex models of sequence evolution.
🧵