Evidence map›Paper›PMID 39738101›Full record

ArticleNature communications2024

Multivariate stochastic modeling for transcriptional dynamics with cell-specific latent time using SDEvelo.

Xu Liao, Lican Kang, Yihao Peng, Xiaoran Chai, Peng Xie, Chengqi Lin, Hongkai Ji, Yuling Jiao, Jin Liu

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  3. Review
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  7. Review
  8. Tet1 safeguards lineage allocation in intestinal stem cells.bioRxiv : the preprint server for biology · 2025
    Article
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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

9 authors.

Xu Liao *School of Data Science, The Chinese University of Hong Kong-Shenzhen, Shenzhen, China.ORCID 0000-0003-1851-4395
Lican Kang *Institute for Math and AI, Wuhan University, Wuhan, China.
Yihao PengSchool of Data Science, The Chinese University of Hong Kong-Shenzhen, Shenzhen, China.
Xiaoran ChaiCancer and Stem Cell Biology Program, Duke-NUS Medical School, Singapore, Singapore.
Peng XieSchool of Biological Science & Medical Engineering, Southeast University, Nanjing, China.ORCID 0000-0002-9509-7268
Chengqi LinKey Laboratory of Developmental Genes and Human Disease, School of Life Science and Technology, Southeast University, Nanjing, China.ORCID 0000-0002-2121-584X
Hongkai JiDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.ORCID 0000-0002-6480-0141
Yuling JiaoSchool of Artificial Intelligence, Wuhan University, Wuhan, China. yulingjiaomath@whu.edu.cn.ORCID 0000-0003-2762-0421
Jin LiuSchool of Data Science, The Chinese University of Hong Kong-Shenzhen, Shenzhen, China. liujinlab@cuhk.edu.cn.ORCID 0000-0002-5707-2078

Funding

National Natural Science Foundation of China (National Science Foundation of China) 12371283National Natural Science Foundation of China (National Science Foundation of China) 12371441
6 · The paper itself

Abstract

Recently, RNA velocity has driven a paradigmatic change in single-cell RNA sequencing (scRNA-seq) studies, allowing the reconstruction and prediction of directed trajectories in cell differentiation and state transitions. Most existing methods of dynamic modeling use ordinary differential equations (ODE) for individual genes without applying multivariate approaches. However, this modeling strategy inadequately captures the intrinsically stochastic nature of transcriptional dynamics governed by a cell-specific latent time across multiple genes, potentially leading to erroneous results. Here, we present SDEvelo, a generative approach to inferring RNA velocity by modeling the dynamics of unspliced and spliced RNAs via multivariate stochastic differential equations (SDE). Uniquely, SDEvelo explicitly models inherent uncertainty in transcriptional dynamics while estimating a cell-specific latent time across genes. Using both simulated and four scRNA-seq and spatial transcriptomics datasets, we show that SDEvelo can model the random dynamic patterns of mature-state cells while accurately detecting carcinogenesis. Additionally, the estimated gene-shared latent time can facilitate many downstream analyses for biological discovery. We demonstrate that SDEvelo is computationally scalable and applicable to both scRNA-seq and sequencing-based spatial transcriptomics data.

Indexed as

Single-Cell AnalysisStochastic ProcessesAlgorithmsCell DifferentiationGene Expression ProfilingHumansModels, GeneticMultivariate AnalysisRNASequence Analysis, RNATranscription, GeneticRNA

Identifiers

PMID39738101
PMCPMC11685993

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.