Evidence map›Paper›PMID 36869080›Full record

ArticleCommunications biology2023

Deep-Manager: a versatile tool for optimal feature selection in live-cell imaging analysis.

A Mencattini, M D'Orazio, P Casti, M C Comes, D Di Giuseppe, G Antonelli, J Filippi, F Corsi, L Ghibelli, I Veith and 3 more

Abstract read
In one paragraph

Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

13 authors.

A Mencattini *Department of Electronic Engineering, University of Rome Tor Vergata, 00133, Rome, Italy.ORCID 0000-0002-3753-0457
M D'Orazio *Department of Electronic Engineering, University of Rome Tor Vergata, 00133, Rome, Italy.
P CastiDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133, Rome, Italy.
M C ComesDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133, Rome, Italy.
D Di GiuseppeDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133, Rome, Italy.
G AntonelliDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133, Rome, Italy.
J FilippiDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133, Rome, Italy.
F CorsiInterdisciplinary Center for Advanced Studies on Lab-on-Chip and Organ-on-Chip Applications (IC-LOC), University of Rome Tor Vergata, 00133, Rome, Italy.
L GhibelliDepartment of Biology, University of Rome Tor Vergata, 00133, Rome, Italy.
I VeithInserm U830, Stress and Cancer Lab, Institut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, 75005, Paris, France.
C Di NataleDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133, Rome, Italy.
M C ParriniInserm U830, Stress and Cancer Lab, Institut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, 75005, Paris, France.ORCID 0000-0002-7082-9792
E MartinelliDepartment of Electronic Engineering, University of Rome Tor Vergata, 00133, Rome, Italy. martinelli@ing.uniroma2.it.ORCID 0000-0002-6673-2066

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the major problems in bioimaging, often highly underestimated, is whether features extracted for a discrimination or regression task will remain valid for a broader set of similar experiments or in the presence of unpredictable perturbations during the image acquisition process. Such an issue is even more important when it is addressed in the context of deep learning features due to the lack of a priori known relationship between the black-box descriptors (deep features) and the phenotypic properties of the biological entities under study. In this regard, the widespread use of descriptors, such as those coming from pre-trained Convolutional Neural Networks (CNNs), is hindered by the fact that they are devoid of apparent physical meaning and strongly subjected to unspecific biases, i.e., features that do not depend on the cell phenotypes, but rather on acquisition artifacts, such as brightness or texture changes, focus shifts, autofluorescence or photobleaching. The proposed Deep-Manager software platform offers the possibility to efficiently select those features having lower sensitivity to unspecific disturbances and, at the same time, a high discriminating power. Deep-Manager can be used in the context of both handcrafted and deep features. The unprecedented performances of the method are proven using five different case studies, ranging from selecting handcrafted green fluorescence protein intensity features in chemotherapy-related breast cancer cell death investigation to addressing problems related to the context of Deep Transfer Learning. Deep-Manager, freely available at https://github.com/BEEuniroma2/Deep-Manager , is suitable for use in many fields of bioimaging and is conceived to be constantly upgraded with novel image acquisition perturbations and modalities.

Indexed as

ArtifactsImage Processing, Computer-AssistedGreen Fluorescent ProteinsNeural Networks, ComputerSoftwareGreen Fluorescent Proteins

Identifiers

PMID36869080
PMCPMC9984362

What OpenQuestion holds

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Registered trials

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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.