Authors
Ding Bai, Le Song, Eric P Xing
Published in
Bioinformatics (Oxford, England). Volume 42. Issue Supplement_1. Jul 01, 2026.
Abstract
Single-cell foundation models (FMs) pretrained on massive unlabeled scRNA-seq data show strong potential in predicting transcriptional responses to unseen genetic perturbations (e.g. knockouts, variants). However, existing approaches do not effectively transfer pretrained knowledge and overlook the imbalance between perturbation-sensitive and insensitive genes, yielding only marginal improvements over non-pretrained baselines.
To address these limitations, we introduce PertAdapt, a framework that unlocks FMs to accurately predict genetic perturbation effects by integrating a plug-in perturbation adapter and an adaptive loss. The adapter employs a gene-similarity-masked attention mechanism to jointly encode perturbation conditions and contextualized representations of unperturbed cells, enabling more effective knowledge transfer. To better capture differential expression patterns, the adaptive loss dynamically reweights perturbation-sensitive genes relative to global transcriptomic signals. Extensive experiments across seven perturbation datasets, including both single- and double-gene settings, demonstrate that PertAdapt consistently outperforms non-pretrained and FM baselines. Moreover, PertAdapt demonstrates strong capacity to model multiplexed gene interactions, to generalize in limited-data regimes, and to maintain robustness across backbone sizes.
Code is available at https://github.com/BaiDing1234/PertAdapt.
PMID:
42412811
Bibliographic data and abstract were imported from PubMed on 08 Jul 2026.
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