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Sparse Latent Factor Forecaster (SLFF) with Iterative Inference for Transparent Multi-Horizon Commodity Futures Prediction

arXiv:2505.06795v5 Announce Type: replace-cross Abstract: Amortized variational inference in latent-variable forecasters creates a deployment gap: the test-time encoder approximates a training-time optimization-refined latent, but without access to future targets. This gap introduces unnecessary forecast error and interpretability challenges. In this work, we propose the Sparse Latent Factor Forecaster with Iterative Inference (SLFF), addressing this through (i) a sparse coding objective with L1 regularization for low-dimensional latents, (ii) unrolled proximal gradient descent (LISTA-style) for iterative refinement during training, and (iii) encoder alignment to ensure amortized outputs match optimization-refined solutions. Under a linearized decoder assumption, we derive a design-motivating bound on the amortization gap based on encoder-optimizer distance, with convergence rates under mild conditions; empirical checks confirm the bound is predictive for the deployed MLP decoder. To prevent mixed-frequency data leakage, we introduce an information-set-aware protocol using release calendars and vintage macroeconomic data. Interpretability is formalized via a three-stage protocol: stability (Procrustes alignment across seeds), driver validity (held-out regressions against observables), and behavioral consistency (counterfactuals and event studies). Using commodity futures (Copper, WTI, Gold; 2005--2025) as a testbed, SLFF demonstrates significant improvements over neural baselines at 1- and 5-day horizons, yielding sparse factors that are stable across seeds and correlated with observable economic fundamentals (interpretability remains correlational, not causal). Code, manifests, diagnostics, and artifacts are released.
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Cardinality-Preserving Attention Channels for Graph Transformers in Molecular Property Prediction

arXiv:2602.02201v4 Announce Type: replace-cross Abstract: Molecular property prediction is crucial for drug discovery when labeled data are scarce. This work presents \modelname, a graph transformer augmented with a query-conditioned cardinality-preserving attention (CPA) channel that retains dynamic support-size signals complementary to static centrality embeddings. The approach combines structured sparse attention with Graphormer-inspired biases (shortest-path distance, centrality, direct-bond features) and unified dual-objective self-supervised pretraining (masked reconstruction and contrastive alignment of augmented views). Evaluation on 11 public benchmarks spanning MoleculeNet, OGB, and TDC ADMET demonstrates consistent improvements over protocol-matched baselines under matched pretraining, optimization, and hyperparameter tuning. Rigorous ablations confirm CPA's contributions and rule out simple size shortcuts. Code and reproducibility artifacts are provided.
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