Evidence map›Paper›PMID 36673072›Full record

ArticleDiagnostics (Basel, Switzerland)2023

A Novel Multi-Task Learning Network Based on Melanoma Segmentation and Classification with Skin Lesion Images.

Fayadh Alenezi, Ammar Armghan, Kemal Polat

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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, 1 synthesis or guideline pooled it.

  1. Diagnosis melanoma with artificial intelligence systems: A meta-analysis study and systematic review.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
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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

3 authors.

Fayadh AleneziDepartment of Electrical Engineering, College of Engineering, Jouf University, Sakaka 72388, Saudi Arabia.ORCID 0000-0002-4099-1254
Ammar ArmghanDepartment of Electrical Engineering, College of Engineering, Jouf University, Sakaka 72388, Saudi Arabia.ORCID 0000-0002-9062-7493
Kemal PolatDepartment of Electrical and Electronics Engineering, Bolu Abant Izzet Baysal University, Bolu 14280, Turkey.

Funding

Al Jouf University DSR2022-RG-0112
6 · The paper itself

Abstract

Melanoma is known worldwide as a malignant tumor and the fastest-growing skin cancer type. It is a very life-threatening disease with a high mortality rate. Automatic melanoma detection improves the early detection of the disease and the survival rate. In accordance with this purpose, we presented a multi-task learning approach based on melanoma recognition with dermoscopy images. Firstly, an effective pre-processing approach based on max pooling, contrast, and shape filters is used to eliminate hair details and to perform image enhancement operations. Next, the lesion region was segmented with a VGGNet model-based FCN Layer architecture using enhanced images. Later, a cropping process was performed for the detected lesions. Then, the cropped images were converted to the input size of the classifier model using the very deep super-resolution neural network approach, and the decrease in image resolution was minimized. Finally, a deep learning network approach based on pre-trained convolutional neural networks was developed for melanoma classification. We used the International Skin Imaging Collaboration, a publicly available dermoscopic skin lesion dataset in experimental studies. While the performance measures of accuracy, specificity, precision, and sensitivity, obtained for segmentation of the lesion region, were produced at rates of 96.99%, 92.53%, 97.65%, and 98.41%, respectively, the performance measures achieved rates for classification of 97.73%, 99.83%, 99.83%, and 95.67%, respectively.

Indexed as

deep learningmelanoma classification and segmentationmulti-task learning networksuper-resolution

Identifiers

PMID36673072
PMCPMC9857507

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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.