Evidence map›Paper›PMID 42704667›Full record

ArticleBioinformatics (Oxford, England)2026

DECANT: decoupling mechanism from context in single-cell drug perturbation representation.

Ren Qi, Wenjie Teng, Xin Yang, Yue Cheng, Alexey K Shaytan, Bin Liu

Abstract read
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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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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ren QiSchool of Computer Science and Technology, Beijing Institute of Technology, Beijing 100081, China.
Wenjie TengSchool of Computer Science and Technology, Beijing Institute of Technology, Beijing 100081, China.
Xin YangSchool of Computer Science and Technology, Beijing Institute of Technology, Beijing 100081, China.
Yue ChengZhongguancun Academy, Beijing 100094, China.
Alexey K ShaytanDepartment of Biology, Lomonosov Moscow State University, Moscow 119991, Russia.
Bin LiuSchool of Computer Science and Technology, Beijing Institute of Technology, Beijing 100081, China.ORCID 0000-0003-3685-9469

Funding

Lomonosov Moscow State UniversityNational Natural Science Foundation of China 62325202National Natural Science Foundation of China 62372332National Natural Science Foundation of China 62572052Zhongguancun Academy 02012502
6 · The paper itself

Abstract

motivationSingle-cell chemical perturbation profiling offers a powerful opportunity to organize drugs by shared mechanism-associated transcriptional responses, but observed transcriptional responses are entangled with contextual variation from cell identity, dose, and treatment time. As a result, models that perform well in perturbation-response prediction may still learn latent spaces dominated by context-associated structure rather than transferable drug-associated signal. We developed DECANT to learn mechanism-aligned perturbation representations that remain stable across context shifts while preserving response fidelity.

resultsDECANT represents each perturbation as a matched treated-control cell set and separates a context-suppressed, mechanism-aligned perturbation representation from context-dependent response information. The resulting mechanism-aligned perturbation space is shaped to support drug-level retrieval and biological interpretation. Under a fixed drug-level unseen-compound benchmark, DECANT achieved the strongest overall response-difference profile among adapted published perturbation models and strong pseudo-bulk baselines across gene- and program-level metrics. Beyond prediction, DECANT produced embeddings that remained stable across changes in dose, cell line, and treatment time, recovered drug neighborhoods enriched for shared mechanism-family annotations, and linked these neighborhoods to interpretable downstream consequence programs. Ablation analyses showed that mechanism-context decoupling provided the main signal-separation backbone, whereas retrieval-oriented shaping was critical for organizing local representation-space geometry. These results support DECANT as a framework for learning context-robust, mechanism-aligned perturbation representations from single-cell transcriptional responses, providing a basis for mechanism-aligned perturbation analysis and representation-based compound prioritization. AVAILABILITY AND IMPLEMENTATION: The DECANT web server is publicly available at http://bliulab.net/DECANT. All source code and analysis scripts are available at https://github.com/bliulab/DECANT and archived on Zenodo at https://doi.org/10.5281/zenodo.21216567.

Indexed as

Computational BiologySingle-Cell AnalysisSoftwareHumans

Identifiers

PMID42704667
PMCPMC13587831

What Socratic holds

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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.