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Samuel King
@Stanford Doctorant en bio-ingénierie / IA biologique dans le laboratoire de @BrianHie @arcinstitute
Je suis tout à fait d'accord avec Jason - les barrières expérimentales posent certains des plus grands défis pour la génomique synthétique, j'espère voir beaucoup de progrès dans ce domaine dans un avenir proche !

Jason Kelly17 sept. 2025
Love this project!! Congrats @samuelhking, @pdhsu and the @arcinstitute crew!
my 2 cents:
AI being used for biological design is best thought of as a translator. Allowing us to speak in English and have it translated into DNA and vice versa. We don't know how to design a phage out of parts but Evo 1/2 were trained by "reading" over 2 million phage genomes from nature and so it learned to "speak" phage DNA. So then we could ask it to generate one -- just like you could ask ChatGPT to generate a poem for you in Chinese even if you don't speak it yourself.
We had already trained AI models on the language of proteins with models like Alphafold and ESM and that worked well -- this paper shows we can do it at a higher level of complexity. This AI model speaks multi-gene phage genomes, not just individual genes. Very exciting demonstration and the work nicely proves it by actually making and testing designed phages. They work!
There are two things that are obvious future directions in my opinion and that will ultimately be successful:
(1) The model should be re-trained based on what it learns about the phages that were designed so it can get better at understanding what the human is asking for and translating that into DNA. This "reinforcement learning" is similar to how Google taught AI models to play chess - you let the model play a game and then tell it if it won or lost. Here you'd let the model design millions of phages, build them in the lab, and then tell it the performance of the different designs.
(2) We should see if models trained on millions of bacterial genomes can enable us to build an AI-designed whole bacterial cell similar to what was done here for a phage. This will see if we can go from translating an English request into a DNA book (500,000 letters of DNA for the simplest bacteria) rather than the DNA poem of the phage (5,000 letters of DNA in a phage).
This would be a nation-scale scientific milestone as cells are the building blocks of all life and the US should make sure we get to it first.
In order to do both (1) and (2) we need dramatic improvements in the efficiency of doing the actual wet lab biology needed to build DNA and test the performance of organisms. It's indicative that they only built 302 phage designs and tested 16 designs -- that's because wet lab work is too slow and expensive. The answer to that is lab automation -- I've been happy to see NSF investing $100M in AI-controllable, automated cloud labs and other efforts that will make US scientific infrastructure more efficient and industrial scale. The White House AI action plan called out the need for these "cloud-enabled labs" too.
Again, awesome work !!!
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Reconnaissant d'être à Arc, c'était le meilleur endroit pour ce travail !

Arc Institute17 sept. 2025
Dans un nouveau préprint du laboratoire de @brianhie, l'équipe rapporte le premier design génératif de génomes de bactériophages viables.
En s'appuyant sur Evo 1 et Evo 2, ils ont généré des séquences de génome entier, aboutissant à 16 phages viables avec des architectures génomiques distinctes.

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De nombreuses fonctions parmi les plus complexes et utiles en biologie émergent à l'échelle des génomes entiers.
Aujourd'hui, nous partageons notre prépublication "Conception générative de nouveaux bactériophages avec des modèles de langage génomique", où nous validons les premiers génomes générés par IA fonctionnels 🧵
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