Evidence map›Paper›PMID 36745648›Full record

ArticlePloS one2023

Combined segmentation and classification-based approach to automated analysis of biomedical signals obtained from calcium imaging.

Gizem Dursun, Dunja Bijelić, Neşe Ayşit, Burcu Kurt Vatandaşlar, Lidija Radenović, Abdulkerim Çapar, Bilal Ersen Kerman, Pavle R Andjus, Andrej Korenić, Ufuk Özkaya

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. 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
0.6field-weighted citation impact, top 31% of its field
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, 4 citations in OpenAlex.

  1. Article
  2. Review
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 at 5 institutions in 3 countries.

Gizem DursunElectrical and Electronics Engineering Department, Süleyman Demirel University, Isparta, Turkey.
Dunja BijelićCenter for Laser Microscopy, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Neşe AyşitDepartment of Medical Biology, Regenerative and Restorative Medicine Research Center (REMER), Research Institute for Health Sciences and Technologies (SABITA), School of Medicine, Istanbul Medipol University, Istanbul, Turkey.
Burcu Kurt VatandaşlarDepartment of Medical Biology, Regenerative and Restorative Medicine Research Center (REMER), Research Institute for Health Sciences and Technologies (SABITA), School of Medicine, Istanbul Medipol University, Istanbul, Turkey.
Lidija RadenovićCenter for Laser Microscopy, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Abdulkerim ÇaparInformatics Institute of İstanbul Technical University, İstanbul, Turkey.
Bilal Ersen KermanDepartment of Medical Biology, Regenerative and Restorative Medicine Research Center (REMER), Research Institute for Health Sciences and Technologies (SABITA), School of Medicine, Istanbul Medipol University, Istanbul, Turkey.ORCID 0000-0003-1106-3288
Pavle R AndjusCenter for Laser Microscopy, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Andrej KorenićCenter for Laser Microscopy, Faculty of Biology, University of Belgrade, Belgrade, Serbia.ORCID 0000-0001-9476-7445
Ufuk ÖzkayaElectrical and Electronics Engineering Department, Süleyman Demirel University, Isparta, Turkey.ORCID 0000-0002-3520-1975
University of Belgrade · RSIstanbul Medipol University · TRSüleyman Demirel University · TRIstanbul Technical University · TRUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Automated screening systems in conjunction with machine learning-based methods are becoming an essential part of the healthcare systems for assisting in disease diagnosis. Moreover, manually annotating data and hand-crafting features for training purposes are impractical and time-consuming. We propose a segmentation and classification-based approach for assembling an automated screening system for the analysis of calcium imaging. The method was developed and verified using the effects of disease IgGs (from Amyotrophic Lateral Sclerosis patients) on calcium (Ca2+) homeostasis. From 33 imaging videos we analyzed, 21 belonged to the disease and 12 to the control experimental groups. The method consists of three main steps: projection, segmentation, and classification. The entire Ca2+ time-lapse image recordings (videos) were projected into a single image using different projection methods. Segmentation was performed by using a multi-level thresholding (MLT) step and the Regions of Interest (ROIs) that encompassed cell somas were detected. A mean value of the pixels within these boundaries was collected at each time point to obtain the Ca2+ traces (time-series). Finally, a new matrix called feature image was generated from those traces and used for assessing the classification accuracy of various classifiers (control vs. disease). The mean value of the segmentation F-score for all the data was above 0.80 throughout the tested threshold levels for all projection methods, namely maximum intensity, standard deviation, and standard deviation with linear scaling projection. Although the classification accuracy reached up to 90.14%, interestingly, we observed that achieving better scores in segmentation results did not necessarily correspond to an increase in classification performance. Our method takes the advantage of the multi-level thresholding and of a classification procedure based on the feature images, thus it does not have to rely on hand-crafted training parameters of each event. It thus provides a semi-autonomous tool for assessing segmentation parameters which allows for the best classification accuracy.

Indexed as

CalciumDiagnostic ImagingAlgorithmsHumansImage Processing, Computer-AssistedMachine LearningCalcium

Identifiers

PMID36745648
PMCPMC9901747
OpenAlexW4319293531

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.