Evidence map›Paper›PMID 42126634›Full record

ArticleMolecular genetics and genomics : MGG2026

Comparison between a conventional tool and deep learning models for RNA velocity analysis of scRNA-Seq data.

Matheus Rodrigues Sauda, Ana Beatriz Rodrigues, Maria Letícia de Oliveira Lyra, Rejane Maria Tommasini Grotto, Lei Gu, Tatiana de Campos Melo, Guilherme Targino Valente

Abstract readComparative Study
In one paragraph

Article in Molecular genetics and genomics : MGG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Matheus Rodrigues SaudaLaboratory of Applied Biotechnology, São Paulo State University, Botucatu, 18618-687, Sao Paulo State, Brazil.
Ana Beatriz RodriguesNucleus of Artificial Intelligence of Clinical Hospital of Medical School of Sao Paulo State University, São Paulo State University, Botucatu, 18618-687, Sao Paulo State, Brazil.
Maria Letícia de Oliveira LyraLaboratory of Applied Biotechnology, São Paulo State University, Botucatu, 18618-687, Sao Paulo State, Brazil.
Rejane Maria Tommasini GrottoLaboratory of Applied Biotechnology, São Paulo State University, Botucatu, 18618-687, Sao Paulo State, Brazil.
Lei GuMax Planck Institute for Heart and Lung Research, Ludwigstraße number 43, Bad Nauheim, 61231, Hessen, Germany.
Tatiana de Campos MeloNucleus of Urgency and Emergency of Clinical Hospital of Medical School of Sao Paulo State University, São Paulo State University, Botucatu, 18618-687, Sao Paulo State, Brazil.
Guilherme Targino ValenteLaboratory of Applied Biotechnology, São Paulo State University, Botucatu, 18618-687, Sao Paulo State, Brazil. valentegt@gmail.com.ORCID http://orcid.org/0000-0001-5355-3424

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-Seq) enables analysis of gene expression at single-cell resolution. RNA velocity analysis infers the temporal dynamics of transcriptional states from the relative abundances of spliced/unspliced mRNA quantified via scRNA-Seq. Classical RNA velocity approaches, such as scVelo, implement gene-specific kinetic modeling. Deep learning methods including DeepVelo, VeloVI, LatentVelo, SymVelo, and scTour are based on variational autoencoders (VAEs), which allow to enhance the robustness and accuracy by leveraging nonlinear latent representations. Here, we systematically evaluated the performance of deep learning RNA velocity tools by comparing with the scVelo dynamical model to access the possible advantages of VAE-base methods. For this purpose, public datasets (GSE149689 and GSE203233) were initially processed using a standard scRNA-Seq pipeline. Comparisons among results of selected velocity tools were conducted using cosine similarity of velocity vectors to assess directional concordance, and by mean squared error analysis of trajectory continuity for the deep learning models. Overall, VAE methods produced significant, richer, and more directionally coherent and consistent velocity fields than the classical model. Our findings indicate that deep learning models provide more consistent and biologically plausible cell-state trajectories, although at the expense of higher computational demands and reliance on accurate splicing quantification. Altogether, our results underscore the relevance of VAE-based frameworks to advance RNA velocity analysis while highlighting the need for careful preprocessing.

Indexed as

Deep LearningRNA-SeqSequence Analysis, RNASingle-Cell AnalysisAutoencoderHumansSingle-Cell Gene Expression AnalysisBenchmarkDeep-learningRNA velocitySingle-cell RNA-Seq

Identifiers

PMID42126634
PMCPMC13171692

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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.