Evidence map›Paper›PMID 37735568›Full record

ArticleNature methods2024

Deep generative modeling of transcriptional dynamics for RNA velocity analysis in single cells.

Adam Gayoso, Philipp Weiler, Mohammad Lotfollahi, Dominik Klein, Justin Hong, Aaron Streets, Fabian J Theis, Nir Yosef

Abstract read
In one paragraph

Article in Nature methods, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
–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

87 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  14. Critical illness expands a transcriptionally distinct hypometabolic CD8bioRxiv : the preprint server for biology · 2026
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27 more citing papers are in PubMed but not listed here.

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

8 authors.

Adam Gayoso *Center for Computational Biology, University of California, Berkeley, Berkeley, CA, USA.ORCID http://orcid.org/0000-0001-9537-0845
Philipp Weiler *Institute of Computational Biology, Helmholtz Center Munich, Munich, Germany.ORCID http://orcid.org/0000-0002-0992-7043
Mohammad LotfollahiInstitute of Computational Biology, Helmholtz Center Munich, Munich, Germany.ORCID http://orcid.org/0000-0001-6858-7985
Dominik KleinInstitute of Computational Biology, Helmholtz Center Munich, Munich, Germany.
Justin HongCenter for Computational Biology, University of California, Berkeley, Berkeley, CA, USA.ORCID http://orcid.org/0000-0003-2115-9101
Aaron StreetsCenter for Computational Biology, University of California, Berkeley, Berkeley, CA, USA.ORCID http://orcid.org/0000-0002-3909-8389
Fabian J TheisInstitute of Computational Biology, Helmholtz Center Munich, Munich, Germany. fabian.theis@helmholtz-munich.de.ORCID http://orcid.org/0000-0002-2419-1943
Nir YosefCenter for Computational Biology, University of California, Berkeley, Berkeley, CA, USA. niryosef@berkeley.edu.ORCID http://orcid.org/0000-0001-9004-1225

Funding

OPTICAL, FLUIDIC, AND MOLECULAR TECHNOLOGIES FOR SINGLE-CELL OMICSR35GM124916 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI Aaron Streets · 2017 to 2026
$3.4M
NIGMS NIH HHS R35 GM124916
6 · The paper itself

Abstract

RNA velocity has been rapidly adopted to guide interpretation of transcriptional dynamics in snapshot single-cell data; however, current approaches for estimating RNA velocity lack effective strategies for quantifying uncertainty and determining the overall applicability to the system of interest. Here, we present veloVI (velocity variational inference), a deep generative modeling framework for estimating RNA velocity. veloVI learns a gene-specific dynamical model of RNA metabolism and provides a transcriptome-wide quantification of velocity uncertainty. We show that veloVI compares favorably to previous approaches with respect to goodness of fit, consistency across transcriptionally similar cells and stability across preprocessing pipelines for quantifying RNA abundance. Further, we demonstrate that veloVI's posterior velocity uncertainty can be used to assess whether velocity analysis is appropriate for a given dataset. Finally, we highlight veloVI as a flexible framework for modeling transcriptional dynamics by adapting the underlying dynamical model to use time-dependent transcription rates.

Indexed as

RNATranscriptomeLearningRNA

Identifiers

PMID37735568
PMCPMC10776389

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.