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Improving Molecular Pretraining with Complementary Featurizations

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arxiv 2209.15101 v1 pith:VBRU5UXL submitted 2022-09-29 cs.LG physics.chem-phq-bio.BM

classification cs.LGphysics.chem-phq-bio.BM
keywords molecularfeaturizationspretrainingcomplementarydifferentmocotasksarchitectures
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Molecular pretraining, which learns molecular representations over massive unlabeled data, has become a prominent paradigm to solve a variety of tasks in computational chemistry and drug discovery. Recently, prosperous progress has been made in molecular pretraining with different molecular featurizations, including 1D SMILES strings, 2D graphs, and 3D geometries. However, the role of molecular featurizations with their corresponding neural architectures in molecular pretraining remains largely unexamined. In this paper, through two case studies -- chirality classification and aromatic ring counting -- we first demonstrate that different featurization techniques convey chemical information differently. In light of this observation, we propose a simple and effective MOlecular pretraining framework with COmplementary featurizations (MOCO). MOCO comprehensively leverages multiple featurizations that complement each other and outperforms existing state-of-the-art models that solely relies on one or two featurizations on a wide range of molecular property prediction tasks.

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Cited by 1 Pith paper

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. AdaptMol: Adaptive Fusion from Sequence String to Topological Structure for Few-shot Drug Discovery

    cs.LG 2025-05 conditional novelty 3.0 of 10

    AdaptMol, a prototypical network fusing SMILES and graph features with attention, reports state-of-the-art few-shot molecular property prediction on Tox21, SIDER, and MUV benchmarks.

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