Evidence map›Paper›PMID 28315633›Full record

ArticleBMC bioinformatics2017

Using simulated fluorescence cell micrographs for the evaluation of cell image segmentation algorithms.

Veit Wiesmann, Matthias Bergler, Ralf Palmisano, Martin Prinzen, Daniela Franz, Thomas Wittenberg

Abstract read
In one paragraph

Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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  4. Topological-Preserving Membrane Skeleton Segmentation in Multiplex Immunofluorescence Imaging.Proceedings of SPIE--the International Society for Optical Engineering · 2023
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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

6 authors.

Veit WiesmannFraunhofer Institute for Integrated Circuits IIS, Am Wolfsmantel 33, Erlangen, 91058, Germany. veit.wiesmann@iis.fraunhofer.de.ORCID http://orcid.org/0000-0001-7327-9311
Matthias BerglerFraunhofer Institute for Integrated Circuits IIS, Am Wolfsmantel 33, Erlangen, 91058, Germany.
Ralf PalmisanoOptical Imaging Centre Erlangen (OICE), Hartmannstraße 14, Erlangen, 91052, Germany.
Martin PrinzenFraunhofer Institute for Integrated Circuits IIS, Am Wolfsmantel 33, Erlangen, 91058, Germany.
Daniela FranzFraunhofer Institute for Integrated Circuits IIS, Am Wolfsmantel 33, Erlangen, 91058, Germany.
Thomas WittenbergFraunhofer Institute for Integrated Circuits IIS, Am Wolfsmantel 33, Erlangen, 91058, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundManual assessment and evaluation of fluorescent micrograph cell experiments is time-consuming and tedious. Automated segmentation pipelines can ensure efficient and reproducible evaluation and analysis with constant high quality for all images of an experiment. Such cell segmentation approaches are usually validated and rated in comparison to manually annotated micrographs. Nevertheless, manual annotations are prone to errors and display inter- and intra-observer variability which influence the validation results of automated cell segmentation pipelines.

resultsWe present a new approach to simulate fluorescent cell micrographs that provides an objective ground truth for the validation of cell segmentation methods. The cell simulation was evaluated twofold: (1) An expert observer study shows that the proposed approach generates realistic fluorescent cell micrograph simulations. (2) An automated segmentation pipeline on the simulated fluorescent cell micrographs reproduces segmentation performances of that pipeline on real fluorescent cell micrographs.

conclusionThe proposed simulation approach produces realistic fluorescent cell micrographs with corresponding ground truth. The simulated data is suited to evaluate image segmentation pipelines more efficiently and reproducibly than it is possible on manually annotated real micrographs.

Indexed as

AlgorithmsMicroscopy, FluorescenceAnimalsB-LymphocytesCell ShapeImage Processing, Computer-AssistedMacrophagesMiceMice, Inbred C57BLProtoplastsCell segmentationEvaluationFluorescence microscopyImage analysisSimulation

Identifiers

PMID28315633
PMCPMC5357336

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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.