Evidence map›Paper›PMID 35660922›Full record

ArticleJournal of cell science2022

An interpretable and versatile machine learning approach for oocyte phenotyping.

Gaelle Letort, Adrien Eichmuller, Christelle Da Silva, Elvira Nikalayevich, Flora Crozet, Jeremy Salle, Nicolas Minc, Elsa Labrune, Jean-Philippe Wolf, Marie-Emilie Terret and 1 more

Abstract read
In one paragraph

Article in Journal of cell science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Machine Learning Methods to Characterize Mouse and Human Oocytes.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. 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

11 authors.

Gaelle LetortCenter for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, 75231 Paris, France.ORCID 0000-0002-5866-0322
Adrien EichmullerCenter for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, 75231 Paris, France.
Christelle Da SilvaCenter for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, 75231 Paris, France.
Elvira NikalayevichCenter for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, 75231 Paris, France.
Flora CrozetCenter for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, 75231 Paris, France.
Jeremy SalleUniversité Paris Cité, CNRS, Institut Jacques Monod, 75013 Paris, France.
Nicolas MincUniversité Paris Cité, CNRS, Institut Jacques Monod, 75013 Paris, France.
Elsa LabruneService de Médecine de la Reproduction, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, 69500 Bron, France.
Jean-Philippe WolfTeam 'From Gametes To Birth', Département Développement, Reproduction, Cancer, Institut Cochin, Inserm U1016, CNRS UMR8104, Université de Paris, 22 rue Mechain, 75014 Paris, France.
Marie-Emilie TerretCenter for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, 75231 Paris, France.ORCID 0000-0001-5843-925X
Marie-Hélène VerlhacCenter for Interdisciplinary Research in Biology (CIRB), College de France, CNRS, INSERM, Université PSL, 75231 Paris, France.ORCID 0000-0001-8377-9010

Funding

Agence Nationale de la RechercheAgence Nationale de la Recherche ANR-18-CE13Centre National de la Recherche ScientifiqueCollège de FranceFondation Bettencourt SchuellerFondation pour la Recherche Medicale EQU201903007796Institut National de la Santé et de la Recherche MédicaleInstitut National Du Cancer PL BIO 2016Investissements d'Avenir ANR-10-LABX-54 MEMO LIFE
6 · The paper itself

Abstract

Meiotic maturation is a crucial step of oocyte formation, allowing its potential fertilization and embryo development. Elucidating this process is important for both fundamental research and assisted reproductive technology. However, few computational tools based on non-invasive measurements are available to characterize oocyte meiotic maturation. Here, we develop a computational framework to phenotype oocytes based on images acquired in transmitted light. We trained neural networks to segment the contour of oocytes and their zona pellucida using oocytes from diverse species. We defined a comprehensive set of morphological features to describe an oocyte. These steps were implemented in an open-source Fiji plugin. We present a feature-based machine learning pipeline to recognize oocyte populations and determine morphological differences between them. We first demonstrate its potential to screen oocytes from different strains and automatically identify their morphological characteristics. Its second application is to predict and characterize the maturation potential of oocytes. We identify the texture of the zona pellucida and cytoplasmic particle size as features to assess mouse oocyte maturation potential and tested whether these features were applicable to the developmental potential of human oocytes. This article has an associated First Person interview with the first author of the paper.

Indexed as

Cumulus CellsOocytesAnimalsFemaleHumansMachine LearningMiceOogenesisZona PellucidaCharacterizationMachine learningMaturationOocyteSegmentation

Identifiers

PMID35660922
PMCPMC9377708

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.