Evidence map›Paper›PMID 34836996›Full record

ArticleScientific reports2021

Reduced and stable feature sets selection with random forest for neurons segmentation in histological images of macaque brain.

C Bouvier, N Souedet, J Levy, C Jan, Z You, A-S Herard, G Mergoil, B H Rodriguez, C Clouchoux, T Delzescaux

Abstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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.

C BouvierCEA, CNRS, MIRCen, Laboratoire Des Maladies Neurodégénératives, Université Paris-Saclay, Fontenay-aux-Roses, France.
N SouedetCEA, CNRS, MIRCen, Laboratoire Des Maladies Neurodégénératives, Université Paris-Saclay, Fontenay-aux-Roses, France.
J LevyService de Médecine Physique Et de Réadaptation - APHP Hôpital Raymond Poincaré, Garches, France.
C JanCEA, CNRS, MIRCen, Laboratoire Des Maladies Neurodégénératives, Université Paris-Saclay, Fontenay-aux-Roses, France.
Z YouCEA, CNRS, MIRCen, Laboratoire Des Maladies Neurodégénératives, Université Paris-Saclay, Fontenay-aux-Roses, France.
A-S HerardCEA, CNRS, MIRCen, Laboratoire Des Maladies Neurodégénératives, Université Paris-Saclay, Fontenay-aux-Roses, France.
G MergoilWitsee, Paris, France.
B H RodriguezWitsee, Paris, France.
C ClouchouxCEA, CNRS, MIRCen, Laboratoire Des Maladies Neurodégénératives, Université Paris-Saclay, Fontenay-aux-Roses, France.
T DelzescauxCEA, CNRS, MIRCen, Laboratoire Des Maladies Neurodégénératives, Université Paris-Saclay, Fontenay-aux-Roses, France. thierry.delzescaux@cea.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In preclinical research, histology images are produced using powerful optical microscopes to digitize entire sections at cell scale. Quantification of stained tissue relies on machine learning driven segmentation. However, such methods require multiple additional information, or features, which are increasing the quantity of data to process. As a result, the quantity of features to deal with represents a drawback to process large series or massive histological images rapidly in a robust manner. Existing feature selection methods can reduce the amount of required information but the selected subsets lack reproducibility. We propose a novel methodology operating on high performance computing (HPC) infrastructures and aiming at finding small and stable sets of features for fast and robust segmentation of high-resolution histological images. This selection has two steps: (1) selection at features families scale (an intermediate pool of features, between spaces and individual features) and (2) feature selection performed on pre-selected features families. We show that the selected sets of features are stables for two different neuron staining. In order to test different configurations, one of these dataset is a mono-subject dataset and the other is a multi-subjects dataset to test different configurations. Furthermore, the feature selection results in a significant reduction of computation time and memory cost. This methodology will allow exhaustive histological studies at a high-resolution scale on HPC infrastructures for both preclinical and clinical research.

Indexed as

AlgorithmsMachine LearningAnimalsBrainImage Processing, Computer-AssistedMacacaMicroscopyNeurons

Identifiers

PMID34836996
PMCPMC8626511

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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.