Evidence map›Paper›PMID 40640612›Full record

ArticleMolecular systems biology2025

PerturbNet predicts single-cell responses to unseen chemical and genetic perturbations.

Hengshi Yu, Weizhou Qian, Yuxuan Song, Joshua D Welch

Abstract read
In one paragraph

Article in Molecular systems biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Article
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  15. Article
  16. Article
  17. Learning Genetic Perturbation Effects with Variational Causal Inference.bioRxiv : the preprint server for biology · 2025
    Article
  18. Machine learning to dissect perturbations in complex cellular systems.Computational and structural biotechnology journal · 2025
    Review
  19. Linking transcriptome and morphology in bone cells at cellular resolution with generative AI.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  20. A mini-review on perturbation modelling across single-cell omic modalities.Computational and structural biotechnology journal · 2024
    Review
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

4 authors.

Hengshi Yu *Department of Biostatistics, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID http://orcid.org/0000-0001-9850-9347
Weizhou Qian *Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID http://orcid.org/0000-0003-3884-7920
Yuxuan SongDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID http://orcid.org/0000-0002-5883-1208
Joshua D WelchDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, 48109, USA. welchjd@umich.edu.ORCID http://orcid.org/0000-0002-5869-2391

Funding

Quantitative definition of cell identity from single-cell multi-omic, spatial, and perturbation dataR01HG010883 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Joshua Welch · 2019 to 2026
$4.4M
Predicting the Impact of Genomic Variation on Cellular StatesU01HG011952 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alan P Boyle · 2021 to 2026
$3.8M
HHS | NIH | National Human Genome Research Institute (NHGRI) R01HG010883HHS | NIH | National Human Genome Research Institute (NHGRI) U01HG011952NHGRI NIH HHS R01 HG010883NHGRI NIH HHS U01 HG011952
6 · The paper itself

Abstract

Chemical and genetic perturbations, such as those induced by small molecules and CRISPR, effect complex changes in the molecular states of cells. Despite advances in high-throughput single-cell perturbation screening technology, the space of possible perturbations is far too large to measure exhaustively. Here, we introduce PerturbNet, a flexible deep generative model designed to predict the distribution of cell states induced by unseen chemical or genetic perturbations. PerturbNet accurately predicts gene expression changes in response to unseen small molecules based on their chemical structures while also accounting for key covariates such as dosage and cell type. Moreover, PerturbNet accurately predicts the distribution of single-cell gene expression states following CRISPR activation or CRISPR interference by leveraging gene functional annotations. Our approach significantly outperforms previous methods, particularly for predicting the effects of perturbing completely unseen genes. Finally, we demonstrate for the first time that amino acid sequence embeddings can be used to predict gene expression changes induced by missense mutations. We use PerturbNet to predict the effects of all point mutations in GATA1 and nominate variants that significantly impact the cell state distribution of human hematopoietic stem cells. Using a crystal structure of GATA1 bound to DNA, we validate that these large-effect variants occur in the core DNA-contact region of GATA1 and tend to involve large changes in amino acid side-chain volume.

Indexed as

Computational BiologySingle-Cell AnalysisCRISPR-Cas SystemsGATA1 Transcription FactorGene Expression RegulationHumansMutation, MissenseGATA1 protein, humanGATA1 Transcription FactorDeep Generative ModelGenome EditingHigh-throughput ScreeningPerturbation PredictionSingle-cell Transcriptomics

Identifiers

PMID40640612
PMCPMC12322087

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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.