Evidence map›Paper›PMID 38528035›Full record

ArticleScientific reports2024

Detecting abnormal cell behaviors from dry mass time series.

Romain Bailly, Marielle Malfante, Cédric Allier, Chiara Paviolo, Lamya Ghenim, Kiran Padmanabhan, Sabine Bardin, Jérôme Mars

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Romain BaillyUniv. Grenoble Alpes, CEA, List, F-38000, Grenoble, France.
Marielle MalfanteUniv. Grenoble Alpes, CEA, List, F-38000, Grenoble, France. marielle.malfante@cea.fr.
Cédric AllierUniv. Grenoble Alpes, CEA, Leti, F-38000, Grenoble, France.
Chiara PavioloUniv. Grenoble Alpes, CEA, Leti, F-38000, Grenoble, France.
Lamya GhenimUniv. Grenoble Alpes, INSERM, CEA-IRIG, BGE, Biomics, F-38000, Grenoble, France.
Kiran PadmanabhanInstitut de Génomique Fonctionnelle de Lyon, Univ. Lyon, CNRS/ENS, UMR 5242, Lyon, France.
Sabine BardinInstitut Curie, PSL Research University, CNRS, UMR 144, Molecular Mechanisms of Intracellular Transport, F-75005, Paris, France.
Jérôme MarsUniv. Grenoble Alpes, CNRS, Grenoble-INP, GIPSA-Lab, 38000, Grenoble, France.

Funding

Association Instituts Carnot 101016726
6 · The paper itself

Abstract

The prediction of pathological changes on single cell behaviour is a challenging task for deep learning models. Indeed, in self-supervised learning methods, no prior labels are used for the training and all of the information for event predictions are extracted from the data themselves. We present here a novel self-supervised learning model for the detection of anomalies in a given cell population, StArDusTS. Cells are monitored over time, and analysed to extract time-series of dry mass values. We assessed its performances on different cell lines, showing a precision of 96% in the automatic detection of anomalies. Additionally, anomaly detection was also associated with cell measurement errors inherent to the acquisition or analysis pipelines, leading to an improvement of the upstream methods for feature extraction. Our results pave the way to novel architectures for the continuous monitoring of cell cultures in applied research or bioproduction applications, and for the prediction of pathological cellular changes.

Indexed as

Problem BehaviorSelf-ManagementCell Culture TechniquesCell LineHumansTime Factors

Identifiers

PMID38528035
PMCPMC11350042

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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.