Evidence map›Paper›PMID 26053631›Full record

ArticleThe Journal of comparative neurology2016

Unsupervised lineage-based characterization of primate precursors reveals high proliferative and morphological diversity in the OSVZ.

Michael Pfeiffer, Marion Betizeau, Julie Waltispurger, Sabina Sara Pfister, Rodney J Douglas, Henry Kennedy, Colette Dehay

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Enhancing our brains: Genomic mechanisms underlying cortical evolution.Seminars in cell & developmental biology · 2018
    Review
  8. Review
  9. Genomic divergence and brain evolution: How regulatory DNA influences development of the cerebral cortex.BioEssays : news and reviews in molecular, cellular and developmental biology · 2016
    Review
  10. 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.

Michael PfeifferInstitute of Neuroinformatics, University of Zurich and ETH Zurich, 8057, Zurich, Switzerland.ORCID http://orcid.org/0000-0001-7159-3622
Marion BetizeauStem Cell and Brain Research Institute, INSERM U846, 69500, Bron, France.
Julie WaltispurgerStem Cell and Brain Research Institute, INSERM U846, 69500, Bron, France.
Sabina Sara PfisterInstitute of Neuroinformatics, University of Zurich and ETH Zurich, 8057, Zurich, Switzerland.
Rodney J DouglasInstitute of Neuroinformatics, University of Zurich and ETH Zurich, 8057, Zurich, Switzerland.
Henry KennedyStem Cell and Brain Research Institute, INSERM U846, 69500, Bron, France.
Colette DehayStem Cell and Brain Research Institute, INSERM U846, 69500, Bron, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Generation of the primate cortex is characterized by the diversity of cortical precursors and the complexity of their lineage relationships. Recent studies have reported miscellaneous precursor types based on observer classification of cell biology features including morphology, stemness, and proliferative behavior. Here we use an unsupervised machine learning method for Hidden Markov Trees (HMTs), which can be applied to large datasets to classify precursors on the basis of morphology, cell-cycle length, and behavior during mitosis. The unbiased lineage analysis automatically identifies cell types by applying a lineage-based clustering and model-learning algorithm to a macaque corticogenesis dataset. The algorithmic results validate previously reported observer classification of precursor types and show numerous advantages: It predicts a higher diversity of progenitors and numerous potential transitions between precursor types. The HMT model can be initialized to learn a user-defined number of distinct classes of precursors. This makes it possible to 1) reveal as yet undetected precursor types in view of exploring the significant features of precursors with respect to specific cellular processes; and 2) explore specific lineage features. For example, most precursors in the experimental dataset exhibit bidirectional transitions. Constraining the directionality in the HMT model leads to a reduction in precursor diversity following multiple divisions, thereby suggesting that one impact of bidirectionality in corticogenesis is to maintain precursor diversity. In this way we show that unsupervised lineage analysis provides a valuable methodology for investigating fundamental features of corticogenesis.

Indexed as

Unsupervised Machine LearningAnimalsBrainCell LineageCluster AnalysisGenetic VectorsGreen Fluorescent ProteinsHydrozoaImage Processing, Computer-AssistedImmunohistochemistryMacaca fascicularisMarkov ChainsMicroscopy, ConfocalPattern Recognition, AutomatedStem Cell NicheStem CellsGreen Fluorescent Proteinscell lineagesclusteringcorticogenesisHidden Markov Treesprimate cortex

Identifiers

PMID26053631
PMCPMC4758405

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.