Evidence map›Paper›PMID 41940106›Full record

ArticleFrontiers in artificial intelligence2026

Integration of handcrafted and deep-level features to improve skin disease detection.

Ranjana Kedar, Manoj Kumar Rajagopal

Abstract read
In one paragraph

Article in Frontiers in artificial intelligence, 2026. 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
–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

0 citing papers in PubMed.

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

2 authors.

Ranjana KedarSchool of Electronics Engineering, Vellore Institute of Technology, Chennai, India.
Manoj Kumar RajagopalSchool of Electronics Engineering, Vellore Institute of Technology, Chennai, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As per the World Health Organization, skin disorders are some of the most common health issues, constituting a significant source of non-fatal disease burden and greatly affecting both quality of life and healthcare systems. Melanoma skin cancer is the most fatal disease in the world, and nearly 60,000 people died due to melanoma in 2022. Skin disorders affect millions of people globally and pose a serious threat to public health. These disorders can affect the skin's composition, function, and appearance. To detect and predict skin diseases, a comprehensive physical examination, a review of the patient's medical history, and appropriate laboratory testing are required. Noise, blur, uneven illumination, inadequate feature representation, and overlapping features between distinct skin disorders all reduce the efficacy of skin disease identification. The Skin Disease Detection Network (SDNet), a deep convolutional neural network-based two-way feature depiction system for multiclass skin disease identification, is presented in this study. To depict hierarchical features in skin images, the SDNet employs two parallel arms. The first arm uses a 2D CNN in conjunction with pre-processed original images, while the second arm uses a 1D CNN that accepts Gray Level Co-occurrence Matrix features (GLCM), improved Local Binary Pattern (ILBP), and Histogram of Oriented Gradient (HOG) features to depict texture and shape attributes of skin images. The accuracy, recall, precision, and F1-score of SDNet results are evaluated using the DermNet dataset. The proposed SDNet achieves an overall accuracy of 99.1%, a recall of 99.1%, a precision of 98.96%, and an F1-score of 98.95% for the 5-class skin disease detection, demonstrating a notable improvement over the performance of traditional state-of-the-art methods. This study marks a notable step forward in leveraging the reliability of SDNet for precise and efficient skin disease identification through the Explainable Artificial Intelligence (XAI) approach.

Indexed as

Explainable Artificial Intelligence (XAI)Gray Level Co-occurrence Matrix features (GLCM)Histogram of Oriented Gradient (HOG) featuresimproved Local Binary Pattern (ILBP)Skin Disease Detection Network (SDNet)

Identifiers

PMID41940106
PMCPMC13046710

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.