Evidence map›Paper›PMID 40897731›Full record

ArticleNature communications2025

Prediction of cellular morphology changes under perturbations with a transcriptome-guided diffusion model.

Xuesong Wang, Yimin Fan, Yucheng Guo, Chenghao Fu, Kinhei Lee, Khachatur Dallakyan, Yaxuan Li, Qijin Yin, Yu Li, Le Song

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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

10 authors.

Xuesong Wang *BioMap Research, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0001-9961-0017
Yimin Fan *BioMap Research, Palo Alto, CA, USA.ORCID http://orcid.org/0009-0002-6514-5588
Yucheng Guo *BioMap Research, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0002-0743-0308
Chenghao FuDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID http://orcid.org/0009-0008-7515-1985
Kinhei LeeDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID http://orcid.org/0009-0000-6832-9863
Khachatur DallakyanDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID http://orcid.org/0009-0002-1555-6581
Yaxuan LiDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID http://orcid.org/0009-0007-3985-1573
Qijin YinBioMap Research, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0001-5284-2259
Yu LiDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China. yuli@cuhk.edu.hk.ORCID http://orcid.org/0000-0002-3664-6722
Le SongBioMap Research, Palo Alto, CA, USA. le.song@mbzuai.ac.ae.ORCID http://orcid.org/0000-0002-9655-2787

Funding

Chinese University of Hong Kong (CUHK) 4937025, 4937026, 5501517, 5501329, SHIAE BME-p1-24
6 · The paper itself

Abstract

Investigating cell morphology changes after perturbations using high-throughput image-based profiling is increasingly important for phenotypic drug discovery, including predicting mechanisms of action (MOA) and compound bioactivity. The vast space of chemical and genetic perturbations makes it impractical to explore all possibilities using conventional methods. Here we propose MorphDiff, a transcriptome-guided latent diffusion model that simulates high-fidelity cell morphological responses to perturbations. We demonstrate MorphDiff's effectiveness on three large-scale datasets, including two drug perturbation and one genetic perturbation dataset, covering thousands of perturbations. Extensive benchmarking shows MorphDiff accurately predicts cell morphological changes under unseen perturbations. Additionally, MorphDiff enhances MOA retrieval, achieving an accuracy comparable to ground-truth morphology and outperforming baseline methods by 16.9% and 8.0%, respectively. This work highlights MorphDiff's potential to accelerate phenotypic screening and improve MOA identification, making it a powerful tool in drug discovery.

Indexed as

Cell ShapeDrug DiscoveryModels, BiologicalTranscriptomeAlgorithmsGene Expression ProfilingHigh-Throughput Screening AssaysHumansPhenotype

Identifiers

PMID40897731
PMCPMC12405515

What OpenQuestion holds

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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 OpenQuestion graph.