Evidence map›Paper›PMID 39230694›Full record

ArticleBioinformatics (Oxford, England)2024

scNODE : generative model for temporal single cell transcriptomic data prediction.

Jiaqi Zhang, Erica Larschan, Jeremy Bigness, Ritambhara Singh

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

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3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

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  14. Variational inference of single cell time series.bioRxiv : the preprint server for biology · 2025
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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.

Jiaqi ZhangDepartment of Computer Science, Brown University, Providence, RI 02906, United States.
Erica LarschanCenter for Computational Molecular Biology, Brown University, Providence, RI 02912, United States.
Jeremy BignessCenter for Computational Molecular Biology, Brown University, Providence, RI 02912, United States.
Ritambhara SinghDepartment of Computer Science, Brown University, Providence, RI 02906, United States.

Funding

Deep learning for understanding gene regulation in diseases via 'omics' integrationR35HG011939 · NHGRI · BROWN UNIVERSITY · PI SINGH, RITAMBHARA · 2021 to 2025
$1.9M
NHGRI NIH HHS R35 HG011939NIH HHSNIH HHS 1R35HG011939-01
6 · The paper itself

Abstract

summaryMeasurement of single-cell gene expression at different timepoints enables the study of cell development. However, due to the resource constraints and technical challenges associated with the single-cell experiments, researchers can only profile gene expression at discrete and sparsely sampled timepoints. This missing timepoint information impedes downstream cell developmental analyses. We propose scNODE, an end-to-end deep learning model that can predict in silico single-cell gene expression at unobserved timepoints. scNODE integrates a variational autoencoder with neural ordinary differential equations to predict gene expression using a continuous and nonlinear latent space. Importantly, we incorporate a dynamic regularization term to learn a latent space that is robust against distribution shifts when predicting single-cell gene expression at unobserved timepoints. Our evaluations on three real-world scRNA-seq datasets show that scNODE achieves higher predictive performance than state-of-the-art methods. We further demonstrate that scNODE's predictions help cell trajectory inference under the missing timepoint paradigm and the learned latent space is useful for in silico perturbation analysis of relevant genes along a developmental cell path. AVAILABILITY AND IMPLEMENTATION: The data and code are publicly available at https://github.com/rsinghlab/scNODE.

Indexed as

Single-Cell AnalysisTranscriptomeComputational BiologyDeep LearningGene Expression ProfilingHumans

Identifiers

PMID39230694
PMCPMC11373355

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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.