Evidence map›Paper›PMID 36831953›Full record

ReviewBiosensors2023

Correlative Fluorescence and Raman Microscopy to Define Mitotic Stages at the Single-Cell Level: Opportunities and Limitations in the AI Era.

Csaba Voros, David Bauer, Ede Migh, Istvan Grexa, Attila Gergely Végh, Balázs Szalontai, Gastone Castellani, Tivadar Danka, Saso Dzeroski, Krisztian Koos and 2 more

Abstract readReview
In one paragraph

Review in Biosensors, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. 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

12 authors.

Csaba VorosSynthetic and Systems Biology Unit, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.ORCID 0000-0002-6198-693X
David BauerSynthetic and Systems Biology Unit, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.
Ede MighSynthetic and Systems Biology Unit, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.
Istvan GrexaSynthetic and Systems Biology Unit, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.ORCID 0000-0002-0548-7706
Attila Gergely VéghInstitute of Biophysics, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.
Balázs SzalontaiInstitute of Biophysics, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.
Gastone CastellaniDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Via G. Massarenti 9, I-40126 Bologna, Italy.ORCID 0000-0003-4892-925X
Tivadar DankaSynthetic and Systems Biology Unit, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.
Saso DzeroskiDepartment of Knowledge Technologies, Jozef Stefan Institute, Jamova Cesta 39, SI-1000 Ljubljana, Slovenia.ORCID 0000-0003-2363-712X
Krisztian KoosSynthetic and Systems Biology Unit, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.
Filippo PiccininiDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Via G. Massarenti 9, I-40126 Bologna, Italy.ORCID 0000-0002-0371-7782
Peter HorvathSynthetic and Systems Biology Unit, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nowadays, morphology and molecular analyses at the single-cell level have a fundamental role in understanding biology better. These methods are utilized for cell phenotyping and in-depth studies of cellular processes, such as mitosis. Fluorescence microscopy and optical spectroscopy techniques, including Raman micro-spectroscopy, allow researchers to examine biological samples at the single-cell level in a non-destructive manner. Fluorescence microscopy can give detailed morphological information about the localization of stained molecules, while Raman microscopy can produce label-free images at the subcellular level; thus, it can reveal the spatial distribution of molecular fingerprints, even in live samples. Accordingly, the combination of correlative fluorescence and Raman microscopy (CFRM) offers a unique approach for studying cellular stages at the single-cell level. However, subcellular spectral maps are complex and challenging to interpret. Artificial intelligence (AI) may serve as a valuable solution to characterize the molecular backgrounds of phenotypes and biological processes by finding the characteristic patterns in spectral maps. The major contributions of the manuscript are: (

Indexed as

Artificial IntelligenceSpectrum Analysis, RamanMicroscopy, Fluorescencemachine learningmicroscopymitosisphenotypic discoveryRaman spectroscopysingle-cell analysis

Identifiers

PMID36831953
PMCPMC9953278

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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.