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El conocimiento es extenso y soy pequeña, la vida me da para sorprenderme de todo lo que conozco y por ende lo que no voy a llegar a conocer:
Mis hermanas están leyendo tochos y pensé en acompañarlas
Hermana @redpanda_0: El idiota de Dostoyevsky, aprox 196k palabras
Hermana @lockedoutfun: El conde de Montecristo de Dumas, aprox 464k palabras
Yop: The shock doctrine, de Klein, 144k palabras
Lo lograremos en 2026?
‘Ora. Este es el tipo de gente que piensa:
Si una mujer puede tener a un bebé en 9 meses, pongamos a 2 mujeres y el bebé nace en 4 meses y medio
There’s a really pronounced divide between people who are on the AI side of things and people who are on the biology side of things. Even among people working in AI, the divide persists based on where they’re focused.
The AI side, adherents of scaling laws and the bitter lesson, believe that AI getting better means AI being more capable of novel discoveries in medicine (that go beyond discovering new drugs in well understood targets or speeding up dry lab work etc).
The biology people think the idea of a bitter lesson in biology is kind of ridiculous and that regardless of AI’s capabilities it’s going to be at least 5-10 years until you could hope to reliably simulate human toxicology in silico (right now AI/ML can’t even reliably simulate in vivo studies like binding affinities or functional assays).
Even the most AI pilled of them, who will list all the areas that AI can reduce the time spent on various areas, don’t think the concept of AI discovering novel targets or generating new understanding of causal biology is realistic in the near term. Most, in fact, will readily characterize the assumption that even an “ASI” level model could find cures hidden in our current understanding (without expanding that understanding with significantly more biological data) as patently false.
This was a big part of why we wanted to experience it ourselves by using AI for a (very) small portion of what it can do in biology. It was both mind blowing and revealed some poignant insights into how different the problem of making AI better at something like coding is to the problems of biology.
Even if it unlocked the ability to generate new molecules at a stunning pace, its simulation (in silico) of binding only had 49% accuracy. And if we wanted to improve that, we’d need to feed it back the data from the lab - data that took about 30x as long to get as it took to generate the molecules. And these were tests in a test tube (turn of phrase), imagine how long it would take if we wanted to improve the model with data that required recruiting humans and monitoring their reactions.
Human biology is very complex, and adding a drug - especially a novel drug and doubly so for a novel drug acting on a novel mechanism - means mapping interactions that have nth-order-effects that we don’t have the data to predict. Virtual cells have made advancements enabled by AI, but the perturbations equate to a small fraction of the possible.
This is before you even get into curing disease, especially uniquely human diseases. Brain function involves cellular identities that are unique to humans, meaning animal studies are of little use.
How long does it take to understand what the side effects of chronic administration of a drug in humans are? AI can speed up analyzing the data, or designing the trial or even getting it approved…but it can’t make a 6 month trial complete in 3 months.
I think its important to point out that significant advancements can be made in AI that contribute to biology, while also being realistic about how much it speeds up something as complex as curing a specific cancer or diseases of the brain.
nirvalite retweeted
Pretty unbelievable the head of drug discovery at Anthropic is only now realizing the bottleneck in biotech isn’t actually drug discovery
Where do you go next after reporting from the Strait of Hormuz? For the past three months, Citrini Research, an independent research firm, has been working with our team and an internal research model to see if they could use AI to create a new drug. What follows is an entertaining, candid, and humbling account of a group of motivated nonexperts (or “filthy casuals”, as Citrini would say) trying to tackle a real problem in human health with Claude.
We landed on scorpion neurotoxins, which kill over 3,000 people a year. Of the 211 designs we produced and tested, 17 met our criteria for a binder. None of the designs bound more than one toxin and none have been tested for neutralizing a toxin.
One of my favorite quotes from the piece is: “Our virtual biologist may have compressed a year's worth of work into a couple days, but biology works at the speed of life…Over two days, we watched Claude work through problems at a speed that was difficult to comprehend. For the next two months, we spent much of the time becoming familiar with laboratory turnaround times (This mostly involved sending memes in Slack).”
nirvalite retweeted
'Speed' derives from the Old English 'spēd,' which referred to good fortune/success.
This sense of 'speed' lives on in 'Godspeed':
"God spede you" = "God prosper you"
We hope this brings you up to speed.
Han escuchado la teoría del Internet muerto? Así se siente mi página de Twitter estos días.
Cualquier cosa, por DM en ig.
nirvalite retweeted
Grindr is training its AI on your photos, your age, and your taps by default, without asking. I looked into the company’s record with user data, and where they put the off switch.
nirvalite retweeted
Curiosity often sparks scientific breakthroughs. For 2026 medicine laureate Peter Hegemann, it began with a question: how could a tiny green alga called Chlamydomonas react so rapidly to light?
The Chlamydomonas algae is famous for its ability to swim towards light. When the alga is stirred into a petri dish, the liquid turns a faint green colour. If one side of the dish is illuminated, the green colour moves towards the light source, as the microscopic algae swim towards it. The algae sense the light with an eyespot, a dot on the cell’s surface that contains a light-capturing molecule, retinal.
Hegemann discovered electrical signals in the light-sensitive eyespot that occurred just half a millisecond after illumination, far faster than the response of the human eye. He could only think of one explanation for this ultrafast response: the process must be much simpler than in a human eye. He proposed that a single protein could both detect light and act as an ion channel, an idea initially met with scepticism.
After years of experiments with his colleague Georg Nagel, Hegemann's hypothesis proved to be correct. Together, they discovered proteins that functioned exactly as he had predicted: ion channels that opened in response to light. This breakthrough laid the foundation for optogenetics, a revolutionary technique that allows scientists to control individual nerve cells with light. What began as a question about a microscopic alga ultimately helped transform the field of neuroscience.
Read more about the newly awarded 2026 Nobel Prize in Physiology or Medicine: bit.ly/4jNd5w7
nirvalite retweeted
Why do small dogs live longer than large dog species, and what is the biologic basis of differences in lifespan and healthspan?
Epigenetics.
There's a lot in the methylation pattern of dogs to explain this @ScienceMagazine
science.org/doi/10.1126/scie…
nirvalite retweeted
Anne Carson. “You could whisper down a well. You could write a letter and keep it in a drawer. You could inscribe a curse on a ribbon of lead and bury it in the ground to lie unread for thousands of years. The point is not to find a reader, the point is the telling itself.”
Scientists have debated for decades whether the human brain sprouts new neurons throughout life.
What would it mean if it could?
go.nature.com/4yAy4XL
nirvalite retweeted
We’ve lost an icon. Margaret Hamilton, a computer science pioneer best known for her work at MIT leading development of the flight software for the Apollo missions to the moon, has died at 90. Read about her legacy via MIT News: news.mit.edu/2026/margaret-h…


























