Pith. sign in

REVIEW 1 cited by

Multi-Objective Latent Space Optimization of Generative Molecular Design Models

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2203.00526 v3 pith:UUNXCCJ5 submitted 2022-03-01 cs.LG q-bio.BM

classification cs.LGq-bio.BM
keywords molecularspacedesignefficiencygenerativelatentmethodmolecules
verification ladder T0 review T1 audit T2 compute T3 formal
0 comments
read the original abstract

Molecular design based on generative models, such as variational autoencoders (VAEs), has become increasingly popular in recent years due to its efficiency for exploring high-dimensional molecular space to identify molecules with desired properties. While the efficacy of the initial model strongly depends on the training data, the sampling efficiency of the model for suggesting novel molecules with enhanced properties can be further enhanced via latent space optimization. In this paper, we propose a multi-objective latent space optimization (LSO) method that can significantly enhance the performance of generative molecular design (GMD). The proposed method adopts an iterative weighted retraining approach, where the respective weights of the molecules in the training data are determined by their Pareto efficiency. We demonstrate that our multi-objective GMD LSO method can significantly improve the performance of GMD for jointly optimizing multiple molecular properties.

Discussion (0). Sign in to comment.

Forward citations

Cited by 1 Pith paper

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

  1. Efficient design of rna sequences with desired properties, structure, and motifs using a grammar variational autoencoder

    q-bio.QM 2025-07 reject novelty 3.0 of 10

    RGVAE, a stochastic-context-free-grammar VAE for RNA, can generate sequences satisfying design constraints, but the claimed outperformance over baselines is not convincingly demonstrated.

Pith tools