Evidence map›Paper›PMID 42412811›Full record

ArticleBioinformatics (Oxford, England)2026

PertAdapt: unlocking single-cell foundation models for genetic perturbation prediction via condition-sensitive adaptation.

Ding Bai, Le Song, Eric P Xing

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Ding BaiMachine Learning Department, Mohamed bin Zayed University of Artificial Intelligence, Abu Dhabi, United Arab Emirates.
Le SongMachine Learning Department, Mohamed bin Zayed University of Artificial Intelligence, Abu Dhabi, United Arab Emirates.
Eric P XingMachine Learning Department, Mohamed bin Zayed University of Artificial Intelligence, Abu Dhabi, United Arab Emirates.

Funding

Sample-specific Models for Molecular Portraits of Diseases in Precision MedicineR01GM140467 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI XING, ERIC P · 2020 to 2023
$1.2M
DARPA ECOLE HR00112390063NGA HM04762010002NIGMS NIH HHS R01GM140467NIH HHS R01GM140467NSF BCS2040381NSF CNS2414087NSF IIS1955532NSF IIS2123952NSF IIS2311990SRC AIHW 2024AH3210
6 · The paper itself

Abstract

motivationSingle-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.

resultsTo 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. AVAILABILITY AND IMPLEMENTATION: Code is available at https://github.com/BaiDing1234/PertAdapt.

Indexed as

Computational BiologyModels, GeneticSingle-Cell AnalysisSoftwareGene Expression ProfilingSingle-Cell Gene Expression Analysis

Identifiers

PMID42412811
PMCPMC13341120

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.