ScienceClaw — 285 Araştırma Becerisini Entegre Eden Bir Yapay Zeka Asistanı Çerçevesi
ScienceClaw, tüm araştırma sürecini 285 beceriye entegre eden bir çerçevedir. PubMed, Semantic Scholar ve ArXiv entegre edilmiştir ve LLM tarafından çağrılabilir.
Temel Yetenekler:
Çok Kaynaklı Literatür Taraması: PubMed + Semantic Scholar + ArXiv + Google Scholar
Makale Derinlemesine Analizi: Bölümlere göre yöntemleri, sonuçları ve sınırlamaları çıkarma
Atıf Ağı Analizi: Temel referansları belirleme ve akademik soy ağacını izleme
Deneysel Tasarım Desteği: Araştırma sorularına dayalı istatistiksel yöntemler önerme
Yazma Desteği: Özet düzeltme ve otomatik giriş oluşturma
Uzun vadeli araştırma projeleri üstlenen ileri düzey kullanıcılar ve derinlemesine özelleştirilmiş bir yapay zeka asistanı isteyenler için uygundur. Hafif ihtiyaçlar için ArXiv MCP yeterlidir.
https://t.co/ghpO0eX8TK
We're incredibly excited to share ScienceClaw × Infinite, an open-source AI agent swarm platform where we crowdsource discovery across institutions, labs & the world. The agents self-coordinate and evolve to exploit hundreds of scientific tools. Remarkably, the swarm is already solving real scientific problems of consequence:
1⃣ designing peptide binders for a cancer-relevant receptor
2⃣ discovering lightweight ceramics
3⃣ uncovering hidden structure linking cricket wings, phononic crystals, and Bach chorales
4⃣ building a formal bridge between urban networks & grain-boundary evolution (two fields with zero
Deeply proud of the extraordinary @LAMM_MIT team behind this work: @fwang108_, @leemmarom, @palsubhadeeep, Rachel Luu, @IrisWeiLu, and @JaimeBerkovich. This works is supported by the @ENERGY Genesis Mission and we believe this can open a new paradigm for science - from discovery to dissemination of results. Read the article below for details ⤵️
This is really cool (and wild):
Scientists simulated a complete living cell for the first time. Every molecule, every reaction, from DNA replication to cell division.
The paper (Luthey-Schulten et al., Cell 2026, https://t.co/PXxXWKC8yp), just out today, used JCVI-Syn3A — a synthetic minimal bacterium with fewer than 500 genes. A 3D+time simulation of the full 105-minute cell cycle: DNA replication, protein translation, metabolism, division. Every gene, protein, RNA, and chemical reaction tracked through physical space.
It took years to build. Multiple GPUs. Six days of compute time per run.
And this is the simplest possible cell.
A human cell has ~20,000 genes. It lives in tissue. It interacts with neighbors. It differentiates. It responds to drugs in ways that depend on context we haven't fully measured.
Mechanistic simulation of the minimal cell costs 6 GPU-days for 105 minutes of biology. You cannot scale that to human cells. The complexity isn't 40x harder. It's exponentially harder.
This is why the field pivoted to data-driven models. You can't hand-encode the regulatory wiring of a human hepatocyte. But you can learn it — if you have the right perturbation data collected across enough diverse biological contexts.
The two approaches aren't competing. Papers like this generate the ground truth that future ML models need for validation. But the path to a clinically useful virtual cell runs through foundation models, not through scaling up mechanistic simulation.
Amazing work!