Searcharxiv⌕ Search

arXiv subjects

Justin M. Baker

Publications and source records attributed to Justin M. Baker.

2 recordsLinked to original sources
arXiv2025

Conformational Rank Conditioned Committees for Machine Learning-Assisted Directed Evolution

Machine Learning-assisted directed evolution (MLDE) is a powerful tool for efficiently navigating antibody fitness landscapes. Many structure-aware MLDE pipelines rely on a single conformation or a single committee across all conformations, limiting their ability to separate conformational uncertainty from epistemic uncertainty. Here, we introduce a rank -conditioned committee (RCC) framework that leverages ranked conformations to assign a deep neural network committee per rank. This design enables a principled separation between epistemic uncertainty and conformational uncertainty. We validate our RCC-MLDE approach on SARS-CoV-2 antibody docking, demonstrating significant improvements over baseline strategies. Our results offer a scalable route for therapeutic antibody discovery while directly addressing the challenge of modeling conformational uncertainty.

cs.LG↗
arXiv2025

Boltzmann Graph Ensemble Embeddings for Aptamer Libraries

Machine-learning methods in biochemistry commonly represent molecules as graphs of pairwise intermolecular interactions for property and structure predictions. Most methods operate on a single graph, typically the minimal free energy (MFE) structure, for low-energy ensembles (conformations) representative of structures at thermodynamic equilibrium. We introduce a thermodynamically parameterized exponential-family random graph (ERGM) embedding that models molecules as Boltzmann-weighted ensembles of interaction graphs. We evaluate this embedding on SELEX datasets, where experimental biases (e.g., PCR amplification or sequencing noise) can obscure true aptamer-ligand affinity, producing anomalous candidates whose observed abundance diverges from their actual binding strength. We show that the proposed embedding enables robust community detection and subgraph-level explanations for aptamer ligand affinity, even in the presence of biased observations. This approach may be used to identify low-abundance aptamer candidates for further experimental evaluation.

cs.LG↗