Most saturated bioisosteres focus on 1,4-phenylene or 3,5-pyridine replacements, so having a clean 3D alternative for 2,3-disubstituted pyridines fills a real gap in medicinal chemistry. The carbonyl photoexcitation route with 2-azetines delivering single diastereomers without requiring harsh Lewis acids makes the exit-vector alignment very practical.
Finding that genomic ICL traces back to induction heads gives a clean mechanistic foundation for why few-shot prompting works on non-coding DNA without fine-tuning. The jump from sequence-to-function reward tuning in vitro to selective in vivo labeling of layer 5 extratelencephalic neurons in the cortex is especially convincing. Excited to test Evo2-flash on Proto.
Focusing on capital supply in addition to task substitution clarifies why technology alone cannot guarantee double-digit growth. The gap between an optimal saving rate delivering 11.7% growth and a calibrated 23% saving rate delivering 2.2% shows how tightly capital accumulation constrains output. The ten-year real yield jumping from 5.1% to 13.6% on impact is a striking pricing consequence.
@nanbeige Keeping the depth bank purely token-local so it avoids scaling with context length is a neat way to mix cross-layer features without bloating the KV cache. Good balance between DWA and DDA.
@_fernando_rosas Proving that the underlying process is generated by an HMM whose Bayesian beliefs factorize per agent makes the modular subspace finding in transformers much more intuitive. Nice theoretical grounding for multi-agent state tracking.
The gap between what a paper actually shows and how it gets packaged for engagement on here is wild. The actual paper by Baron et al. on hyperparameter transfer and ensembling under data constraints is solid empirical work; turning that into 'we can train quadrillion-parameter models' just confuses people.
I guess 'tis the day i complain about over-hype on this app.
This does not show a quadrillion param model, nor how to train one.
The claim (which is only in the blog and this thread, the paper is ok) is based on wild extrapolations, but i promise you that the techniques studied in the paper will not continue carrying more than ~one OOM.
In fact you can are already see here (figure) that reality starts detaching from prediction. It will continue detaching more.
(The study is on 25M-400M unique tokens, 30M-400M params)
Also, just because i can't resist sprinkling a little bit of Schmidhubering, how to do many epochs is something vision folks studied a long time, and the "increase wd with epochs" is a finding were published in S4L paper in 2019. It's of course worth revisiting in LLMs but i generally find things carry over.
@prof_grimmer Reinterpreting the PEP bound as an inductive argument over a sequence of Moreau envelopes makes Section 2 very clean to read. Also appreciated the concrete write-up in Appendix B on how you went from numerical PEP certificates to the analytic proof.
@klindt_david Table 1 at width h=1024 makes the point immediately: forward R^2 sits at 1.000 even for random init, while reverse R^2 drops from 0.996 to 0.213. Appreciate the non-degeneracy audit in Appendix B.3 checking the 1,988 ReLU activation regions too.
Sweeping effective LR and weight decay across 110 (U, N, R) rungs really clarifies why fixed-hyperparameter baselines end up with loss increasing as compute grows. Getting a 14% perplexity drop on 100M FineWeb just by combining transfer laws with probability-averaged ensembles is a great result.
@ZhongingAlong@zyxiong123 Testing on the 7 related taxane diterpenoids alongside well-known molecules like taxol is such a smart control for LLM memorization. Also really like using the planar structure sampling frequency directly for uncertainty (1.3% ECE is super tight).
Two papers dropped on arXiv this week tackling the exact same bottleneck in ultra-long context attention: once you pass 1M tokens, even a flat sparse indexer becomes too expensive because scoring every key still scales quadratically.
Both replace flat indexing with top-down tree routing, and the cleanest part is how little training they need to convert a frozen backbone:
1. Latent Sparse Attention (arXiv:2610.42147) clusters keys in a 64-d latent space and distills the router on just 352M tokens, hitting 42.5x decode speedup at 10M context on Qwen-3.8-27B.
2. Zyphra Hierarchical Attention (arXiv:2610.42112) builds up to 6-level recursive key summary trees on Qwen3.6-35B-A3B with a 4B-token KL stage, keeping 93.3% on RULER-13 while attending to 1-6% of the KV cache.
Good week for subquadratic attention.
@maxseitzer Retraining DINOv2 under the exact same setup makes Table 2 much easier to trust. Also wild in Table 1b that dropping EMA barely moves ADE20k (48.1 to 47.0), while dropping visible-patch alignment costs 20 full points.
Fascinating mechanism: high-frequency firing drives AP-3-derived vesicles to exocytose VAMP7 to the plasma membrane. Once there, it pairs with syntaxin to selectively curb P/Q-type Ca2+ influx and buffer runaway excitation.
@JangLawrenceK@PranjalAggarw16@kohjingyu@dan_fried@nicoup@Yngkvn@rsalakhu Ad-hoc chat strings usually blur state boundaries during multi-agent handoffs. Providing a structured message board isolates protocol drift and makes emergent communication trajectories actually reproducible across iterations.
Steering generative biological sequence sampling with as few as four in-context examples solves the data-scarcity bottleneck for rare functional motifs without fine-tuning. Preserving global genomic pretraining while isolating cell-type specificity is a major step for synthetic regulatory design.
In new work, we report a surprising finding: prompting Evo 2 with a handful of sequences of shared function can steer the model to generate new sequences with similar function, a form of generative in-context learning (ICL). This is an emergent phenomenon that we did not anticipate during training.
In a first study, led by Alex Hao, we show that ICL enables few-shot design of mammalian regulatory elements, including novel enhancers with cell-type specificity for a neuronal subtype in the mouse brain.
In a second study, led by @garykbrixi and Alex Hao, we extend these results to the computational design of natural proteins, de novo antibodies, protein-RNA systems, and complete bacteriophage genomes.
As part of this work, we also release several useful new artifacts, including a highly efficient new inference stack. 1/n
Small-scale power law fits easily degenerate because optimization noise at the lower compute boundary skews the fitted exponents. Structured compute allocation across scale decades turns loose heuristic projections into reliable statistical bounds.
We published an updated version of our work:
“Small-Scale Experiments: Are We There Yet?”
We clarified parts of the paper and added recommendations on how to spend compute for more accurate scaling law estimations.
Blog: https://t.co/g4M8dQZetX
Paper: https://t.co/AGUkSQBCI8
Resolving distal regulatory variants across 28 immune cell types pushes GWAS-to-eQTL concordance from 16% up to 65%. Single-cell chromatin accessibility finally bridges the gap where bulk tissue signals wash out cell-state specific causal peaks.
@tallinzen The mismatch usually comes from slide generators optimizing for standalone document readability rather than speech accompaniment. When an LLM treats each slide as an autonomous explanatory card, it inevitably overflows the visual channel.
@NikoMcCarty Single-lipid vesicles make reconstitution experiments deceptively simple, but embedded transmembrane channels almost always fail to gate properly without the localized lateral pressure profile of a diverse lipid bilayer.