Evidence map›Paper›PMID 30464314›Full record

ArticleScientific reports2018

Machine learning based classification of cells into chronological stages using single-cell transcriptomics.

Sumeet Pal Singh, Sharan Janjuha, Samata Chaudhuri, Susanne Reinhardt, Annekathrin Kränkel, Sevina Dietz, Anne Eugster, Halil Bilgin, Selçuk Korkmaz, Gökmen Zararsız and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Metabolomic-based aging clocks.npj metabolic health and disease · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Biomarkers of aging.Science China. Life sciences · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Genome-scale transcriptional dynamics and environmental biosensing.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Article
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

12 authors.

Sumeet Pal SinghCenter for Molecular and Cellular Bioengineering, TU Dresden, Dresden, 01307, Germany. sumeet_pal.singh@tu-dresden.de.ORCID http://orcid.org/0000-0002-5154-3318
Sharan JanjuhaCenter for Molecular and Cellular Bioengineering, TU Dresden, Dresden, 01307, Germany.
Samata ChaudhuriMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, 01307, Germany.
Susanne ReinhardtCenter for Molecular and Cellular Bioengineering, TU Dresden, Dresden, 01307, Germany.
Annekathrin KränkelCenter for Molecular and Cellular Bioengineering, TU Dresden, Dresden, 01307, Germany.
Sevina DietzCenter for Molecular and Cellular Bioengineering, TU Dresden, Dresden, 01307, Germany.
Anne EugsterCenter for Molecular and Cellular Bioengineering, TU Dresden, Dresden, 01307, Germany.
Halil BilginDepartment of Computer Engineering, Abdullah Gül University, Kayseri, 38030, Turkey.
Selçuk KorkmazDepartment of Biostatistics and Medical Informatic, Trakya University, Edirne, 22030, Turkey.
Gökmen ZararsızDepartment of Biostatistics, Erciyes University, Kayseri, 38030, Turkey.
Nikolay NinovCenter for Molecular and Cellular Bioengineering, TU Dresden, Dresden, 01307, Germany.
John E ReidMRC Biostatistics Unit, University of Cambridge, Cambridge, CB2 0SR, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-associated deterioration of cellular physiology leads to pathological conditions. The ability to detect premature aging could provide a window for preventive therapies against age-related diseases. However, the techniques for determining cellular age are limited, as they rely on a limited set of histological markers and lack predictive power. Here, we implement GERAS (GEnetic Reference for Age of Single-cell), a machine learning based framework capable of assigning individual cells to chronological stages based on their transcriptomes. GERAS displays greater than 90% accuracy in classifying the chronological stage of zebrafish and human pancreatic cells. The framework demonstrates robustness against biological and technical noise, as evaluated by its performance on independent samplings of single-cells. Additionally, GERAS determines the impact of differences in calorie intake and BMI on the aging of zebrafish and human pancreatic cells, respectively. We further harness the classification ability of GERAS to identify molecular factors that are potentially associated with the aging of beta-cells. We show that one of these factors, junba, is necessary to maintain the proliferative state of juvenile beta-cells. Our results showcase the applicability of a machine learning framework to classify the chronological stage of heterogeneous cell populations, while enabling detection of candidate genes associated with aging.

Indexed as

Gene Expression ProfilingMachine LearningAge FactorsAnimalsCytological TechniquesHumansInsulin-Secreting CellsSingle-Cell AnalysisZebrafish

Identifiers

PMID30464314
PMCPMC6249247

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.