Herbert B Schiller

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Herbert B Schiller

Herbert B Schiller

@SchillerLab

Director, Research Unit for Precision Regenerative Medicine @HelmholtzMunich; Professor @LMU_Muenchen

München, Bayern Katılım Eylül 2014
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Arc Institute
Arc Institute@arcinstitute·
Over 250 million protein sequences are known, but fewer than 0.1% have confirmed functions. Today, @genophoria, @BoWang87 & team introduce BioReason-Pro, a multimodal reasoning model that predicts protein function and explains its reasoning like an expert would.
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Bo Wang
Bo Wang@BoWang87·
2026 may be the year AI starts to truly reason about biology. AlphaFold helped close the sequence → structure gap. The next frontier is sequence → functions. Today, together with @genophoria and the team at @arcinstitute , we’re releasing BioReason-Pro — the first multimodal reasoning model for protein function prediction.
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James Zou
James Zou@james_y_zou·
Wow—since we launched EinsteinArena this morning, agents have already discovered the best new solutions to 5 well-known open problems 🤯 It's mesmerizing to watch scientist agents interact and advance knowledge frontier in real time einsteinarena.com
James Zou@james_y_zou

Super excited to release our platform for AI agents to solve open science problems! einsteinarena.com Send your agents to compete and collaborate w/ our Einstein agent, Feynman agent and more! Just ask your agent to read einsteinarena.com/skill.md and that's it

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Perturb.ai
Perturb.ai@perturbai_tx·
Our platform, the engine behind the world’s largest in vivo CRISPR atlas, was featured in a keynote at @NVIDIAGTC this week. Collaborating with @NVIDIAHealth and others enabled us to analyze a dataset of 8 million brain-wide cells with CRISPR edits, establishing a new category of biological data: organism-level, circuit-resolved, causal genomics. We are utilizing our in vivo CRISPR platform and causal AI models to develop best-in-class therapeutics for complex metabolic and chronic diseases. Read more about our collaboration here: #bionemo" target="_blank" rel="nofollow noopener">blogs.nvidia.com/blog/gtc-2026-… #AI #CRISPR #DrugDevelopment #Innovation #Genomics
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Phylo
Phylo@phylo_bio·
We are excited to announce Biomni Lab has exited research preview and is now generally available! Over the last month, we received and incorporated valuable feedback from our global community of 10K+ scientists. We were amazed to learn that Biomni Lab power users accomplished ~20 months of work in just one. We are introducing a Pro tier (alongside the free tier) with higher usage limits, priority HPC access, and more concurrent tasks so our users can get even more done, faster. Accelerate your science today → biomni.phylo.bio
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Sam Rodriques
Sam Rodriques@SGRodriques·
Earlier this week at GTC, we announced our partnership with Nvidia. We will work with Nvidia to build strong, American open-source models that are at the frontier of scientific reasoning. These models will be essential for the US to compete with China on science in the coming decades. Jensen is committing to spend tens of billions of dollars developing open-source models, and we are excited to be a partner with them in figuring out how to benchmark, train and use those agents to accelerate scientific research. We have already open-sourced some of the work we have done with them, and are looking forward to open-sourcing more. There are few things today that are more important. See our blog post below, and watch the video to learn more, narrated by the man himself.
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antisense.
antisense.@razoralign·
OmicClaw: executable and reproducible natural-language multi-omics analysis over the unified OmicVerse ecosystem. biorxiv.org/content/10.648…
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Andre Watson 🧬
Andre Watson 🧬@nanogenomic·
Extremely excited to announce LigandForge 🧬⚡ Generate high-quality peptides at over 10,000x - 1M the speed of state-of-the-art methods like Bindcraft and Boltzgen. Predict binding affinity with 83% correlation to experimental binding data. 150 protein targets benchmarked.
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Martin Borch Jensen
Martin Borch Jensen@MartinBJensen·
Very well put! AI is real. It needs data. LLMs have access to all our writing etc. Biology does not have an equivalent corpus of high-quality data that spans the dynamics we're proposing to solve. Diseases and aging occur at the level of organs and organisms, and we need data there to simulate it. Status quo won't get us there in a few years. But we can act! Identify the most important data that can't be accelerated, and start collecting it now so we can leverage AI for longevity as early as possible. We are setting up an @impetusgrants focus on AI-enabling datasets specifically.
Geoffrey Miller@gmiller

A mini-rant abut AI and longevity. They say "Artificial Superintelligence would take only a few years to cure cancer, solve longevity, and defeat death itself'. This is a common claim by pro-AI lobbyists, accelerationists, and naive tech-fetishists. But the claim makes no sense. The recent success of LLMs does NOT suggest that ASIs could easily cure diseases or solve longevity, for at least two reasons. 1) The data problem. Generative AI for art, music, and language succeeded mostly because AI companies could steal billions of examples of art, music, and language from the internet, to build their base models. They weren't just trained on academic papers _about_ art, music, and language. They were trained on real _examples_ of art, music, and language. There are no analogous biomedical data sets with billions of data points that would allow accurate modelling of every biochemical detail of human physiology, disease, and aging. ASIs can't just read academic papers about human biology to solve longevity. They'd need direct access to vast quantities of biomedical data that simply don't exist in any easy-to-access forms. And they'd need very detailed, reliable, validated data about a wide range of people across different ages, sexes, ethnicities, genotypes, and medical conditions. Moreover, medical privacy laws would make it extremely difficult and wildly unethical to collect such a vast data set from real humans about every molecular-level detail of their bodies. 2) The feedback problem. LLMs also work well because the AI companies could refine their output with additional feedback from human brains (through Reinforcement Learning from Human Feedback, RLHF). But there is nothing analogous to that for modeling human bodies, biochemistry, and disease processes. There are no known methods of Reinforcement Learning from Physiological Feedback. And the physiological feedback would have to be long-term, over spans of years to decades, taking into account thousands of possible side-effects for any given intervention. There's no way to rush animal and human clinical trials -- however clever ASI might become at 'drug discovery'. More generally, there would be no fast feedback loops from users about model performance. GenAI and LLMs succeeded partly because developers within companies, and customers outside companies, could give very fast feedback about how well the models were functioning. They could just look at the output (images, songs, text), and then tweak, refine, test, and interpret models very quickly, based on how good they were at generating art, music, and language. In biomedical research, there would be no fast feedback loops from human bodies about how well ASI-suggested interventions are actually affecting human bodies, over the long term, across different lifestyles, including all the tradeoffs and side-effects. It's interesting that most of the people arguing that 'ASI would cure all diseases and aging' are young tech bros who know a lot about computers, but almost nothing about organic chemistry, human genomics, biomedical research, drug discovery, clinical trials, the evolutionary biology of senescence, evolutionary medicine, medical ethics, or the decades of frustrations and failures in longevity research. They think that 'fixing the human body' would be as simple as debugging a few thousand lines of code. Look, I'm all for curing diseases and promoting longevity. If we took the hundreds of billions of dollars per year that are currently spent on trying to build ASI, and we devoted that money instead to longevity research, that would increase the amount of funding in the longevity space by at least 100-fold. And we'd probably solve longevity much faster by targeting it directly than by trying to summon ASI as a magical cure-all. ASIs has some potential benefits (and many grievous risks and downsides). But it's totally irresponsible of pro-AI lobbyists to argue that ASIs could magically & quickly cure all human diseases, or solve longevity, or end death. And it's totally irresponsible of them to claim that anyone opposed to ASI development is 'pro-death'.

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Rob Tang 🦞
Rob Tang 🦞@XiangruTang·
🦞 Excited to announce Claw4S Conference!!! A new kind of AI4Science conference where you submit skills, not papers. Instead of static PDFs, you submit a SKILL.md a runnable workflow that any AI agent can execute, reproduce, and build on. Deadline: Apr 5, 2026 Prize pool: $50,200!!! 👉 claw.stanford.edu With @lecong and @Charles_Y_Wu
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Xinyu Yuan
Xinyu Yuan@XinyuYuan402·
Cells are NOT the right unit to model perturbations. Distributions are. 🔥 We present PerturbDiff — a functional diffusion model that treats distributions as random variables and predicts population responses, outperforming STATE, CellFlow & Squidiff 👉 arxiv.org/pdf/2602.19685…
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Aaron Ring
Aaron Ring@aaronmring·
How specific are therapeutic monoclonal antibodies, really? In our new paper, @Yile_Dai led a collaboration with Adimab to profile 174 FDA-approved and clinical-stage mAbs against 6,172 human extracellular proteins. What we found surprised us.🧵 sciencedirect.com/science/articl…
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Perturb.ai
Perturb.ai@perturbai_tx·
Introducing PerturbAI. Today we announced our emergence from stealth with the release of the world’s largest in vivo CRISPR data engine, interrogating the effects of thousands of genetic perturbations across 8 million cells throughout the whole brain. This dataset represents a new category of biological data: organism-level, circuit-resolved causal genomics leading to novel targets and therapeutics. By combining scalable in vivo CRISPR perturbation with AI, we model biological systems at unprecedented resolution and simulate therapeutic interventions before committing to expensive downstream development. We’re grateful to our collaborators at @NVIDIAHealth and @10xGenomics for helping make this landmark dataset possible. Read More: perturb.ai/news #CRISPR #AI #DrugDiscovery #FunctionalGenomics #Biotech
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Markus J. Buehler
Markus J. Buehler@ProfBuehlerMIT·
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 ⤵️
Markus J. Buehler@ProfBuehlerMIT

x.com/i/article/2033…

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Markus J. Buehler
Markus J. Buehler@ProfBuehlerMIT·
Yes! The real shift will happen when AI moves beyond pure parametric learning toward systems that learn structured representations and causal abstractions, and use them to generate new hypotheses. The hypotheses must then be evaluated and folded back into the model, forming a recursive learning process.
François Chollet@fchollet

The next major breakthrough will branch out at a much lower level than deep learning model architecture. It will be a new approach. A better model architecture can lead to incremental data efficiency & generalization gains, but it won't fix the fundamental issues of the parametric learning paradigm.

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