🇨🇦 Vancouver

Canada
Joined April 2010
Love it
Today we announced the Claude-led discovery of a molecular machine that we suspect could represent a new gene editing mechanism. Its precise function, biotechnological utility (if any), or level of significance is not yet clear, but at minimum it is work I would have been proud to do as a PhD student. The work was done mostly, though not entirely, by Claude: our life sciences team suggested a broad area of research, Claude read through the literature and a bunch of genome data and discovered something interesting, then Claude proposed experiments to verify the discovery and our team carried them out. It’s easy to dismiss this as a one-off or curiosity, but we’ve repeatedly seen a pattern where AI performance in new intellectual domains goes from weak to superhuman in a matter of a few years. In 2023 models struggled to do math at the level of an average high-school student. In 2024 they started to do well on math competitions for the best high-schoolers in the country, in 2025 they started to solve minor open problems, in early 2026 more significant open problems, and in late 2026 they are beginning to solve the top few open problems in all of mathematics. We believe AI for biology is on a similar exponential trend. The main difference between biology and mathematics, of course, is that math can be done purely theoretically, while biology requires experimentation. Some have used this to draw the conclusion that AI’s utility in biology will be limited. We think this is wrong. As we’ve demonstrated today, humans can collaborate with AI to perform the experiments, validate key results in a few weeks and, if necessary, work with the AI to iterate on what they find. Eventually it may even be possible for Claude itself to safely perform the experiments by autonomously controlling lab equipment, with appropriate safeguards in place, but we aren’t doing that today (our lab is also a BSL1/BSL2 facility that doesn't handle materials dangerous to humans). More broadly, biomedical advancement has many stages — from fundamental biology discoveries, to translational research, to drug discovery, clinical trials, and finally the actual delivery of medicines and health care to patients. We are also interested in these later stages, but even simply accelerating the first stage of fundamental biological discoveries has the potential to speed up and broaden the entire pipeline. Improving our understanding of biology and sharpening biologists’ tools can drive forward all of the later stages, for example by identifying new drug targets, finding new therapeutic modalities, allowing for more precise measurement, and speeding up the experimental loop which itself further accelerates our understanding of biology. This will not in itself speed up clinical trial times, but if it succeeds it could greatly increase the number of promising candidates that go into the pipeline — an increase in throughput even though latency remains. In Machines of Loving Grace, I wrote about AI’s potential to “cure most diseases in 5-10 years” — a goal that sounds impossible, but one I believe is just barely possible if AI is applied to every stage of the pipeline. The first step is showing that AI can first help with, and then drive, biological discoveries. Claude’s discovery is the latest in a line of related prior work that goes back decades, beginning with systems like CRISPR, and continuing with discoveries like the bridge recombinase and VIPR in the past few years. Recently, there has been heightened interest in systems based on reverse transcriptase (RT) enzymes, the enzyme underlying the system Claude identified. And most recently, a Stanford team working independently described a novel RT system with an associated non-coding array that is in some ways similar to the one Claude found, though they are distinct systems that evolved independently from each other. I believe that we’re at the very beginning of finding such systems and developing them into powerful tools for biotechnology. I’m proud of the resources Anthropic has invested in accelerating the public benefits of AI through the life sciences, and we’re aiming both to grow our life sciences team and to work with other scientists to extend this approach to a broad range of problems. If you have a proposal for a research collaboration or are interested in joining our life sciences team, please reach out.
121
First impressions - loving ULT app - need better integration with Onchain wallet - it assigns you a new wallet and one needs to transfer funds there (2) should be able to accept CRO on cronos as funding source , right now only takes USDC and swapping CRO to USDC is a headache
30
Opus 5.0 or Opus 5.2 ? Any takers
144
did something funny ! CODEX was taking too long to execute a task - too many strict Guardrails were in place, which was making it very difficult to execute and complete the job. Too many checks and balances. I asked it to delegate some tasks to Fable
2
34
Whereas Fable gets the job done quickly
1
Both CODEX and Fable started to communicate via an MD file, checking that file every 30 seconds to communicate between the two and delegate tasks between the two. it WORKED ! try it if you have both subscriptions. Codex, although a very good engineer, is very strict
15
Get ready for I have been testing fabel 5.1 as early tester for 2 weeks now and it’s an incredible model —- posts dropping soon
1
48
How will you resolve the liquidity crunch on CRO- there are so many crypto dot com chain - like EVM POS CRO ETH - a normal person will struggle to understand what drives what ? And then when you figure something out - than look at the slippage on dollar ? @Fwiz @CronosApp
51
ID: 5581584628808018 if that helps @Alibaba_Qwen
23
IMRAN - Zebracross retweeted
We’ve received notice that the Department of Commerce has lifted export controls on Claude Fable 5 and Mythos 5. We'll begin restoring access tomorrow, and will share an update soon. We’re grateful to our users for their patience, and to everyone who worked with us on redeploying the models.
4,000
12,646
7,035
83,725
15,182,325
IMRAN - Zebracross retweeted
When Ethereum hits $5,000 I will give 1 ETH to ten people who follow me. The rules are simple: - like this tweet, follow me and RT - comment “5k incoming” Let’s go! $ETH
13,262
9,368
515
14,747
1,145,735
IMRAN - Zebracross retweeted
This is Mars! 140 million miles away from us!
1,200
1,464
181
15,575
2,241,004
IMRAN - Zebracross retweeted
Claude Code can run multiple agents in parallel and synthesize them together at the end. In case you didn't know.
25
30
3
461
75,956
IMRAN - Zebracross retweeted
This is literally your AI startup team now: Product → Deep Search w/ Grok 3, Gemini 2.5, ChatGPT o3 Eng → Cursor + Gemini 2.5 MAX, Replit Agent, Codex GTM → Bolt, Lovable, Veo 3 Ops → ChatGPT Scheduled Tasks, Vertex AI Agent Builder Bookmark this! 🧵👇
75
212
13
1,507
239,574
IMRAN - Zebracross retweeted
Here comes another validation about PAF J-10C taking out 3x Rafales in Bvr combat with Pl-15. Air forces around the world are studying the Bvr tactics of PAF that how can a smaller force smoke top of line all types of Bvr capable jets of adversary deep inside their own airspace
33
100
4
431
18,611
IMRAN - Zebracross retweeted
“Yes, Pakistan did destroy the S-400 at Adampur but more importantly, we intercepted most of their missile strikes” ~ General Anil Chauhan, India’s CDS
105
452
23
2,777
128,953
IMRAN - Zebracross retweeted
This is fatal strike of Pakistani hypersonic Anti Radar missile on S-400 air defense system's Cheeseboard Radar in Adampur air base. First video shows missile blasting towards the system the second video shows a successful hit.
273
1,637
277
5,571
2,421,342