Evidence map›Paper›PMID 30397207›Full record

ArticleScientific reports2018

Deep Analysis of Mitochondria and Cell Health Using Machine Learning.

Atena Zahedi, Vincent On, Rattapol Phandthong, Angela Chaili, Guadalupe Remark, Bir Bhanu, Prue Talbot

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 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Deep learning analysis of urine-derived stem cell mitochondrial morphology as a non-invasive Alzheimer's disease biomarker.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Mitochondrial heterogeneity in diseases.Signal transduction and targeted therapy · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

7 authors.

Atena ZahediGraduate Program in Bioengineering, University of California, Riverside, CA., USA.
Vincent OnDepartment of Electrical & Computer Engineering, University of California, Riverside, CA., USA.
Rattapol PhandthongDepartment of Molecular, Cell and Systems Biology, University of California, Riverside, CA., USA.
Angela ChailiDepartment of Molecular, Cell and Systems Biology, University of California, Riverside, CA., USA.
Guadalupe RemarkDepartment of Molecular, Cell and Systems Biology, University of California, Riverside, CA., USA.
Bir BhanuGraduate Program in Bioengineering, University of California, Riverside, CA., USA.ORCID http://orcid.org/0000-0001-8971-6416
Prue TalbotGraduate Program in Bioengineering, University of California, Riverside, CA., USA. talbot@ucr.edu.

Funding

Metals in Electronic Cigarette Aerosol R01DA036493 · NIDA · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI TALBOT, PRUDENCE · 2014 to 2018
$3.6M
Do Electronic Cigarettes Reduce Harm?R21DA037365 · NIDA · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI TALBOT, PRUDENCE · 2014 to 2015
$408k
NIDA NIH HHS R01 DA036493NIDA NIH HHS R21 DA037365
6 · The paper itself

Abstract

There is a critical need for better analytical methods to study mitochondria in normal and diseased states. Mitochondrial image analysis is typically done on still images using slow manual methods or automated methods of limited types of features. MitoMo integrated software overcomes these bottlenecks by automating rapid unbiased quantitative analysis of mitochondrial morphology, texture, motion, and morphogenesis and advances machine-learning classification to predict cell health by combining features. Our pixel-based approach for motion analysis evaluates the magnitude and direction of motion of: (1) molecules within mitochondria, (2) individual mitochondria, and (3) distinct morphological classes of mitochondria. MitoMo allows analysis of mitochondrial morphogenesis in time-lapse videos to study early progression of cellular stress. Biological applications are presented including: (1) establishing normal phenotypes of mitochondria in different cell types; (2) quantifying stress-induced mitochondrial hyperfusion in cells treated with an environmental toxicant, (3) tracking morphogenesis in mitochondria undergoing swelling, and (4) evaluating early changes in cell health when morphological abnormalities are not apparent. MitoMo unlocks new information on mitochondrial phenotypes and dynamics by enabling deep analysis of mitochondrial features in any cell type and can be applied to a broad spectrum of research problems in cell biology, drug testing, toxicology, and medicine.

Indexed as

Machine LearningA549 CellsComputational BiologyHumansMitochondriaMovementPhenotypeSeleniumStress, PhysiologicalSupervised Machine LearningSelenium

Identifiers

PMID30397207
PMCPMC6218515

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.