NMRAgent is an evidential LLM agent for NMR-based molecular structure elucidation that improves accuracy on novel scaffolds and demonstrates utility on real natural products.
hub Mixed citations
ChemBERTa: large -scale self -supervised pretraining fo r molecular property prediction
Mixed citation behavior. Most common role is background (40%).
29
Pith papers citing it
Background
40% of classified citations
hub tools
citation-role summary
background 2
method 2
baseline 1
citation-polarity summary
representative citing papers
scCycleMol adds a learnable circular cell-cycle head with closed-loop supervision from predicted treated expression, yielding higher r-squared on SciPlex3 gene predictions and improved phase accuracy versus ChemCPA baselines.
LOGICA adds context to pretrained biological LMs via logit-space contrastive alignment with gated adapters, improving AUC on held-out drug-resistance mutation ranking from ~0.55 to ~0.65 while preserving token likelihoods.
MolGram integrates a conditional n-gram memory module into molecular language models to address locality gaps in SMILES tokenization, improving performance on generation, forward prediction, and retrosynthesis while outperforming 3x larger baselines.
Chem-GMNet uses sphere-native embeddings, DualSKA attention, and SH-FFN layers to match or beat ChemBERTa-2 on MoleculeNet tasks with fewer parameters and sometimes no pretraining.
FORGE reformulates molecular optimization as context-aware fragment ranking and replacement using mined low-to-high edit pairs, outperforming larger language models and graph methods on standard benchmarks.
Chirality emerges in SMILES translation models through an abrupt encoder-centered reorganization of representations after a long plateau, identified via checkpoint analysis and ablation.
Pre-training improves CLMs' encoding of molecular substructures especially in upper layers while fine-tuning selectively modifies task-relevant substructures more than others.
Sparse autoencoders on MolFormer reveal position-tracking latents in early layers and atom-in-substructure plus pharmacologically relevant features in later layers, with non-canonical SMILES causing greater representation disruption than invalid ones.
Closed-loop LM-agent auto research finds some transferable gains on molecular property prediction benchmarks via external data but shows non-transfer for model and feature edits selected on validation.
Decentralized AI agent teams self-organize around hypotheses, critique proposals, and share knowledge to outperform single-agent baselines on biomedical ML, language-model optimization, and protein fitness tasks.
Drug-blind cancer sensitivity prediction is limited by evaluation metric and training distribution rather than drug representation complexity.
PolyLM fine-tunes a 9B-parameter LLM on 185k papers to predict polymer properties from text alone, achieving median R² of 0.74 on 68k held-out samples.
Chemically meaningful steering for properties like cLogP and TPSA emerges in entangled Transformer-VAE latent spaces only after controlling for SELFIES representation confounds through residualization and decoded traversals.
Benchmark across 78 endpoint-split entries finds classical ML winning 47.4% of best performances over pretrained models, GNNs, and LLMs, with performance depending on model-task-split fit rather than scale.
NOSE aligns molecular, receptor, and linguistic modalities in a shared embedding space via tri-modal orthogonal contrastive learning and weak positive samples, achieving SOTA performance and zero-shot generalization on olfactory tasks.
FlexMS is a new flexible benchmarking framework that lets researchers dynamically combine deep learning architectures and evaluate their mass spectrum prediction performance on public metabolomics datasets using multiple metrics and retrieval tasks.
MIST models up to 10x larger than prior work, fine-tuned on over 400 structure-property tasks, match or exceed SOTA on benchmarks and demonstrate zero-shot olfactory perception mapping consistent with hyperbolic geometry.
SmellNet supplies 828k gas-sensor time series across 50 substances plus 43 mixtures; ScentFormer reaches 63.3% top-1 accuracy on classification and 50.2% top-1@0.1 on mixture prediction.
ChemCrow augments LLMs with 18 expert chemistry tools to autonomously plan and execute syntheses and guide molecular discoveries in organic synthesis, drug discovery, and materials design.
UltraNMR is a large foundation model pre-trained on 158M simulated NMR spectra that transfers to experimental data, achieving SOTA on structure analysis tasks and enabling a 94M-molecule spectral library plus real-world natural product elucidation.
MolE-RAG is a training-free RAG framework that augments LLMs with literature, molecular context, and structural analogs to improve performance on nine molecular property prediction tasks.
A tabular foundation model pipeline with ETF preprocessing transfers across 7 modalities on 95 datasets, matching lightweight tuned baselines on frozen features at much higher speed while providing calibration for deployment.
SPADE selects ligands more efficiently than deep learning or Bayesian optimization, needing fewer tests on average to identify high-quality drug candidates for novel proteins.
citing papers explorer
-
Towards Generalizable and Evidential Nuclear Magnetic Resonance-Based Molecular Structure Elucidation via Large Language Model Agent
NMRAgent is an evidential LLM agent for NMR-based molecular structure elucidation that improves accuracy on novel scaffolds and demonstrates utility on real natural products.
-
Modeling Cell-Cycle-Aware Single-Cell Drug Perturbation Responses
scCycleMol adds a learnable circular cell-cycle head with closed-loop supervision from predicted treated expression, yielding higher r-squared on SciPlex3 gene predictions and improved phase accuracy versus ChemCPA baselines.
-
Contextualizing Biological Language Models across Modalities via Logit-Space Contrastive Alignment
LOGICA adds context to pretrained biological LMs via logit-space contrastive alignment with gated adapters, improving AUC on held-out drug-resistance mutation ranking from ~0.55 to ~0.65 while preserving token likelihoods.
-
Augmenting Molecular Language Models with Local $n$-gram Memory
MolGram integrates a conditional n-gram memory module into molecular language models to address locality gaps in SMILES tokenization, improving performance on generation, forward prediction, and retrosynthesis while outperforming 3x larger baselines.
-
Chem-GMNet: A Sphere-Native Geometric Transformer for Molecular Property Prediction
Chem-GMNet uses sphere-native embeddings, DualSKA attention, and SH-FFN layers to match or beat ChemBERTa-2 on MoleculeNet tasks with fewer parameters and sometimes no pretraining.
-
FORGE: Fragment-Oriented Ranking and Generation for Context-Aware Molecular Optimization
FORGE reformulates molecular optimization as context-aware fragment ranking and replacement using mined low-to-high edit pairs, outperforming larger language models and graph methods on standard benchmarks.
-
From Syntax to Semantics: Unveiling the Emergence of Chirality in SMILES Translation Models
Chirality emerges in SMILES translation models through an abrupt encoder-centered reorganization of representations after a long plateau, identified via checkpoint analysis and ablation.
-
Probing Chemical Language Models: Effects of Pre-training and Fine-tuning
Pre-training improves CLMs' encoding of molecular substructures especially in upper layers while fine-tuning selectively modifies task-relevant substructures more than others.
-
What Does a Chemical Language Model Know About Molecules?
Sparse autoencoders on MolFormer reveal position-tracking latents in early layers and atom-in-substructure plus pharmacologically relevant features in later layers, with non-canonical SMILES causing greater representation disruption than invalid ones.
-
Closed-loop Auto Research for Molecular Property Prediction: Discovering and Certifying Generalizable Improvements
Closed-loop LM-agent auto research finds some transferable gains on molecular property prediction benchmarks via external data but shows non-transfer for model and feature edits selected on validation.
-
AutoScientists: Self-Organizing Agent Teams for Long-Running Scientific Experimentation
Decentralized AI agent teams self-organize around hypotheses, critique proposals, and share knowledge to outperform single-agent baselines on biomedical ML, language-model optimization, and protein fitness tasks.
-
Training distribution determines the ceiling of drug-blind cancer sensitivity prediction
Drug-blind cancer sensitivity prediction is limited by evaluation metric and training distribution rather than drug representation complexity.
-
Can LLMs Predict Polymer Physics Just by Reading Synthesis and Processing Prose?
PolyLM fine-tunes a 9B-parameter LLM on 185k papers to predict polymer properties from text alone, achieving median R² of 0.74 on 68k held-out samples.
-
Molecules Meet Language: Confound-Aware Representation Learning and Chemical Property Steering in Transformer-VAE Latent Spaces
Chemically meaningful steering for properties like cLogP and TPSA emerges in entangled Transformer-VAE latent spaces only after controlling for SELFIES representation confounds through residualization and decoded traversals.
-
Do Larger Models Really Win in Drug Discovery? A Benchmark Assessment of Model Scaling in AI-Driven Molecular Property and Activity Prediction
Benchmark across 78 endpoint-split entries finds classical ML winning 47.4% of best performances over pretrained models, GNNs, and LLMs, with performance depending on model-task-split fit rather than scale.
-
NOSE: Neural Olfactory-Semantic Embedding with Tri-Modal Orthogonal Contrastive Learning
NOSE aligns molecular, receptor, and linguistic modalities in a shared embedding space via tri-modal orthogonal contrastive learning and weak positive samples, achieving SOTA performance and zero-shot generalization on olfactory tasks.
-
FlexMS is a flexible framework for benchmarking deep learning-based mass spectrum prediction tools in metabolomics
FlexMS is a new flexible benchmarking framework that lets researchers dynamically combine deep learning architectures and evaluate their mass spectrum prediction performance on public metabolomics datasets using multiple metrics and retrieval tasks.
-
Foundation Models for Discovery and Exploration in Chemical Space
MIST models up to 10x larger than prior work, fine-tuned on over 400 structure-property tasks, match or exceed SOTA on benchmarks and demonstrate zero-shot olfactory perception mapping consistent with hyperbolic geometry.
-
SmellNet: A Large-scale Dataset for Real-world Smell Recognition
SmellNet supplies 828k gas-sensor time series across 50 substances plus 43 mixtures; ScentFormer reaches 63.3% top-1 accuracy on classification and 50.2% top-1@0.1 on mixture prediction.
-
ChemCrow: Augmenting large-language models with chemistry tools
ChemCrow augments LLMs with 18 expert chemistry tools to autonomously plan and execute syntheses and guide molecular discoveries in organic synthesis, drug discovery, and materials design.
-
A large-scale foundation model enables simulation-to-real adaptation for nuclear magnetic resonance-based molecular structure analysis
UltraNMR is a large foundation model pre-trained on 158M simulated NMR spectra that transfers to experimental data, achieving SOTA on structure analysis tasks and enabling a 94M-molecule spectral library plus real-world natural product elucidation.
-
MolE-RAG: Molecular Structure-Enhanced Retrieval-Augmented Generation for Chemistry
MolE-RAG is a training-free RAG framework that augments LLMs with literature, molecular context, and structural analogs to improve performance on nine molecular property prediction tasks.
-
When Tabular Foundation Models Transfer Across Modalities: A Systematic Evaluation Across 95 Datasets, 7 Modalities, and Two Regimes
A tabular foundation model pipeline with ETF preprocessing transfers across 7 modalities on 95 datasets, matching lightweight tuned baselines on frozen features at much higher speed while providing calibration for deployment.
-
SPADE: Faster Drug Discovery by Learning from Sparse Data
SPADE selects ligands more efficiently than deep learning or Bayesian optimization, needing fewer tests on average to identify high-quality drug candidates for novel proteins.
-
When Active Learning Falls Short: An Empirical Study on Chemical Reaction Extraction
Active learning for chemical reaction extraction frequently produces non-monotonic learning curves and fails to deliver stable gains over random sampling because of strong pretraining, structured CRF decoding, and label sparsity.
-
Lit2Vec: A Reproducible Workflow for Building a Legally Screened Chemistry Corpus from S2ORC for Downstream Retrieval and Text Mining
Lit2Vec delivers a documented, reproducible pipeline that extracts and annotates a large licensed chemistry paper corpus from S2ORC with paragraph embeddings and subfield labels.
-
GLACIER: A Multimodal Student-Teacher Foundation Model for Molecular Property Prediction
GLACIER combines graph, SMILES, and descriptor encoders with Finsler fusion and contrastive distillation to produce an efficient multimodal model for molecular property prediction.
-
Regression with Large Language Models for Materials and Molecular Property Prediction
Fine-tuned LLaMA 3 achieves regression performance on QM9 molecular properties and 28 materials properties from composition strings that rivals random forests but is 5-10x worse than specialized models using atomic coordinates.
-
Machine Learning Based Prediction of Proton Conductivity in Metal-Organic Frameworks
A newly built database of proton-conductive MOFs supports descriptor and transformer machine learning models that predict conductivity with MAE 0.91.