Sherko

Love to play with data 🧩

[Sherko @JustSherko]

@_bluecarnation Chronological Chaos

[Sherko @JustSherko]

@_bluecarnation پس شاید هنر آدم‌ها این باشه که قبل از رسیدن سونامی، زبان بارون رو بفهمن...

[Sherko @JustSherko]

دلتنگی مثل بارون ملایمه، آروم می‌باره و خیس می‌کنه، بدون اینکه داد بزنه...

[Sherko @JustSherko]

ستاره‌ها هیچ‌وقت عجله نمی‌کنن، شاید واسه همینه که هنوز می‌درخشن...

[Sherko @JustSherko]

@AshkanTofangdar اشکان، دیکُد کردن بعضی توییت‌هات سخته:))))

[Sherko @JustSherko]

@aimarketiran وقتی generate رو زدی، یه کم وایسا؛ خودش می‌نویسه generating...
عکس‌ها رو ببین...مثل عکس‌ها رو برو جلو.

[Sherko @JustSherko]

یه ویژگی خفن NotebookLM اینه که می‌تونید وارد یه مکالمه با چند تا دوست مجازی بشید و باهاشون به زبان‌های مختلف، از جمله انگلیسی، صحبت کنید. اگه ارور داد، از نسخه وب استفاده کنید...

به بچه‌های کلاسم هم معرفی‌ش کردم و واقعا دیدم که پیشرفت داشتن...(از گزینه Studio استفاده کنید)

[Sherko @JustSherko]

@luciferm1023 @miniKhorshid نه، OpenVPN ذاتا به معنی داشتن IP ثابت نیست؛ بستگی به نوع کانفیگ و سرور داره...

[Sherko @JustSherko]

صبح که زود بیدار می‌شم، اعتماد به نفسم چندبرابره، چون هنوز هیچ‌کس فرصت نکرده انتظارشو بهم تحمیل کنه.
این ساعت‌ها فقط مال خودمن...

[Sherko @JustSherko]

@hediii12 تو نسخه وب از این مسیر برید

Studio → Audio Overview → Generate → Interactive Mode → Join

[Sherko @JustSherko]

@mohamadi_arch این عالیه،

https://t.co/OXtPAi5rrB

این هم یه منبع فارسی خوب

https://t.co/l1PGvTNyB6

[Sherko @JustSherko]

@omgsidewalks I really missed Skype:((((

[Sherko @JustSherko]

@Loc0m0 پس شاید وقتشه به‌جای حسرت گذشته، حواسمون به ساختن فردا باشه....

[Sherko @JustSherko]

@madbluei فارسی

https://t.co/25aSfW76sH

انگلیسی

https://t.co/yH8JN92Aki

[Sherko @JustSherko]

تجربه‌‌م تو یکی از پروژه‌هام یه نکته داشت:

این AI Agentها تو کدنویسی خیلی خوبن اما تو مسائل پزشکی، کدنویسی به‌تنهایی واسه یه تصمیم قابل‌اعتماد کافی نیست.

کدِ خوب ≠ تصمیمِ درست

تو پردازش سیگنال‌های حیاتی، اعتبارسنجی و نظارت انسانی همچنان ضروریه.

[Sherko @JustSherko]

دوستان، فایلا خیلی سنگینه؛ بدون VPN دانلود کنید!
اگه نتونستین بهم پیام بدین...

[Sherko @JustSherko]

توی گوگل‌درایوم به یه مجموعه خوب واسه یادگیری ماشین (ML) رسیدم؛ با پایتون و از صفر، خیلی ساده توضیح داده شده. شما هم استفاده کنید...
از این دو لینک می‌تونید دانلودشون کنید.

https://t.co/bXVWRA6HAs
https://t.co/9OHYSzfb4I

[Sherko @JustSherko]

الان با صدای خروس بیدار شدم
فقط مونده بود درو باز کنم ببینم مزرعه‌س یا زندگی شهری هنوز سر جاشه... 🐓

[Sherko @JustSherko]

@RonfortMartin Much obliged

[Sherko @JustSherko]

با کمک Claude یه آنزیم جدید رو کشف کردن...
کاش بگن با چه مدلی این کار رو کردن!

[Dario Amodei @DarioAmodei]

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.