Evidence map›Paper›PMID 36141085›Full record

ArticleEntropy (Basel, Switzerland)2022

Brain Tumor Segmentation Based on Bendlet Transform and Improved Chan-Vese Model.

Kexin Meng, Piercarlo Cattani, Francesco Villecco

Open access · goldAbstract read
In one paragraph

Article in Entropy (Basel, Switzerland), 2022. 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
1.3field-weighted citation impact, top 18% 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

0 citing papers in PubMed, 14 citations in OpenAlex.

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

3 authors at 3 institutions in 2 countries.

Kexin MengCollege of Information and Electrical Engineering, China Agricultural University, Beijing 100083, China.
Piercarlo CattaniDepartment of Computer, Control and Management Engineering, University of Rome "La Sapienza", Via Ariosto 25, 00185 Roma, Italy.
Francesco VilleccoDepartment of Industrial Engineering, University of Salerno, via Giovanni Paolo II 132, 84084 Fisciano, Italy.ORCID 0000-0001-6545-4589
China Agricultural University · CNSapienza University of Rome · ITUniversity of Salerno · IT

Funding

Beijing Natural Science Foundation 4172034National Natural Science Foundation of China 61871380Shandong Provincial Natural Science Foundation ZR2020MF019
6 · The paper itself

Abstract

Automated segmentation of brain tumors is a difficult procedure due to the variability and blurred boundary of the lesions. In this study, we propose an automated model based on Bendlet transform and improved Chan-Vese (CV) model for brain tumor segmentation. Since the Bendlet system is based on the principle of sparse approximation, Bendlet transform is applied to describe the images and map images to the feature space and, thereby, first obtain the feature set. This can help in effectively exploring the mapping relationship between brain lesions and normal tissues, and achieving multi-scale and multi-directional registration. Secondly, the SSIM region detection method is proposed to preliminarily locate the tumor region from three aspects of brightness, structure, and contrast. Finally, the CV model is solved by the Hermite-Shannon-Cosine wavelet homotopy method, and the boundary of the tumor region is more accurately delineated by the wavelet transform coefficient. We randomly selected some cross-sectional images to verify the effectiveness of the proposed algorithm and compared with CV, Ostu, K-FCM, and region growing segmentation methods. The experimental results showed that the proposed algorithm had higher segmentation accuracy and better stability.

Indexed as

Bendlet systemfeature setimage expressionsegmentationShannon-cosine wavelet

Identifiers

PMID36141085
PMCPMC9497468
OpenAlexW4293530432

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.