Evidence map›Paper›PMID 35606383›Full record

ArticleNature communications2022

Cell cycle gene regulation dynamics revealed by RNA velocity and deep-learning.

Andrea Riba, Attila Oravecz, Matej Durik, Sara Jiménez, Violaine Alunni, Marie Cerciat, Matthieu Jung, Céline Keime, William M Keyes, Nacho Molina

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
9.8field-weighted citation impact, top 1% of its field
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

63 citing papers in PubMed, 120 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Cell Cycle Sensing Shapes Human T Cell Fate and Exhaustion Programs.bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Stress-dependent growth in breast cancer arises from a mechano-osmotic coupling and cell-sizing checkpoint.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

3 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

10 authors at 1 institution in 2 countries.

Andrea Riba *Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg; Centre National de la Recherche Scientifique (CNRS) UMR 7104; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 1258, 1 Rue Laurent Fries, 67404, Illkirch, France. arriba87@gmail.com.
Attila Oravecz *Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg; Centre National de la Recherche Scientifique (CNRS) UMR 7104; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 1258, 1 Rue Laurent Fries, 67404, Illkirch, France.
Matej DurikInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg; Centre National de la Recherche Scientifique (CNRS) UMR 7104; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 1258, 1 Rue Laurent Fries, 67404, Illkirch, France.
Sara JiménezInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg; Centre National de la Recherche Scientifique (CNRS) UMR 7104; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 1258, 1 Rue Laurent Fries, 67404, Illkirch, France.
Violaine AlunniInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg; Centre National de la Recherche Scientifique (CNRS) UMR 7104; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 1258, 1 Rue Laurent Fries, 67404, Illkirch, France.
Marie CerciatInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg; Centre National de la Recherche Scientifique (CNRS) UMR 7104; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 1258, 1 Rue Laurent Fries, 67404, Illkirch, France.
Matthieu JungInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg; Centre National de la Recherche Scientifique (CNRS) UMR 7104; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 1258, 1 Rue Laurent Fries, 67404, Illkirch, France.
Céline KeimeInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg; Centre National de la Recherche Scientifique (CNRS) UMR 7104; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 1258, 1 Rue Laurent Fries, 67404, Illkirch, France.ORCID http://orcid.org/0000-0001-7604-3814
William M KeyesInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg; Centre National de la Recherche Scientifique (CNRS) UMR 7104; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 1258, 1 Rue Laurent Fries, 67404, Illkirch, France.
Nacho MolinaInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC); Université de Strasbourg; Centre National de la Recherche Scientifique (CNRS) UMR 7104; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR-S 1258, 1 Rue Laurent Fries, 67404, Illkirch, France. molinan@igbmc.fr.ORCID http://orcid.org/0000-0003-0233-3055
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the fact that the cell cycle is a fundamental process of life, a detailed quantitative understanding of gene regulation dynamics throughout the cell cycle is far from complete. Single-cell RNA-sequencing (scRNA-seq) technology gives access to these dynamics without externally perturbing the cell. Here, by generating scRNA-seq libraries in different cell systems, we observe cycling patterns in the unspliced-spliced RNA space of cell cycle-related genes. Since existing methods to analyze scRNA-seq are not efficient to measure cycling gene dynamics, we propose a deep learning approach (DeepCycle) to fit these patterns and build a high-resolution map of the entire cell cycle transcriptome. Characterizing the cell cycle in embryonic and somatic cells, we identify major waves of transcription during the G1 phase and systematically study the stages of the cell cycle. Our work will facilitate the study of the cell cycle in multiple cellular models and different biological contexts.

Indexed as

Deep LearningSingle-Cell AnalysisGene Expression ProfilingGenes, cdcRNASequence Analysis, RNATranscriptomeRNA

Identifiers

PMID35606383
PMCPMC9126911
OpenAlexW4281297170

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.