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ASSESSMENT OF HIGH-DIMENSIONAL DATA CLASSIFICATION FOR SKIN MALIGNANCY DETECTION USING DEEP LEARNING

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ASSESSMENT OF HIGH-DIMENSIONAL DATA CLASSIFICATION FOR SKIN MALIGNANCY DETECTION USING DEEP LEARNING

ORDINARY APPLICATION

Published

date

Filed on 28 October 2024

Abstract

Abstract Skin cancer can be detected through visual screening and skin analysis based on the biopsy and pathological state of the human body. Automated methods of skin malignancy classification determine the defined changeability of the presence of those lesions. The survival rate of cancer patients is low, and millions of people are diagnosed annually. By determining the different comparative analyses, the skin malignancy classification is evaluated. Using the isomap with the vision transformer, we analyse the high-dimensional images with dimensionality reduction. Skin cancer can present with severe cases and lifethreatening symptoms. * By providing patients with prior intervention, early detection of cancer can reduce the life-threatening phases of the disease. Overall performance evaluation and classification tend to improve the accuracy of the high-dimensional skin lesion dataset when completed. In deep learning methodologies, the distinct phases of skin malignancy classification are determined by its accuracy, specificity, Fl recall, and sensitivity while implementing the classification methodology.A nonlinear dimensionality reduction technique called isomap preserves the data's underlying non-linear relationships intact. This is essential for the categorization of skin malignancies, as the features that separate malignant from benign skin lesions may not be linearly separable. Isomap decreases the data's complexity while maintaining its essential characteristics, making it simpler to analyse and explain the findings. High dimensional datasets for skin lesions have been evaluated and classified more effectively when evaluated and classified using isomap with the (ViT) vision transformer. Keywords:Skin Malignancy, Skin Lesion, High-Dimensional Images, Classification, Deep Learning, Performance Evaluation

Patent Information

Application ID202441082149
Invention FieldBIO-MEDICAL ENGINEERING
Date of Application28/10/2024
Publication Number45/2024

Inventors

NameAddressCountryNationality
PANDIKUMAR SASSOCIATE PROFESSOR, DEPARTMENT OF MCA, ACHARYA INSTITUTE OF TECHNOLOGY, Acharya Dr. Sarvepalli Radhakrishnan Road, BANGALORE, KARNATAKA, India, Pin code-560010.IndiaIndia
SHAHEENA KVASSISTANT PROFESSOR, DEPARTMENT OF MCA, ACHARYA INSTITUTE OF TECHNOLOGY, Acharya Dr. Sarvepalli Radhakrishnan Road, BANGALORE, KARNATAKA, India, Pin code-560010.IndiaIndia
ANILA R.NAMBIARASSISTANT PROFESSOR, DEPARTMENT OF MCA, ACHARYA INSTITUTE OF TECHNOLOGY, Acharya Dr. Sarvepalli Radhakrishnan Road, BANGALORE, KARNATAKA, India, Pin code-560010.IndiaIndia
MUDASSER RASHIDASSISTANT PROFESSOR, DEPARTMENT OF MCA, ACHARYA INSTITUTE OF TECHNOLOGY, Acharya Dr. Sarvepalli Radhakrishnan Road, BANGALORE, KARNATAKA, India, Pin code-560010.IndiaIndia
C M SULAIKHAASSISTANT PROFESSOR&HEAD, DEPARTMENT OF COMPUTER, MTM COLLEGE OF ARTS,SCIENCE AND COMMERCE Street Pazhanji, Veliancode - Maranchery Rd, VELIYANCODE, KERALA, India, Pin code- 679578.IndiaIndia
ARUN M .ASSISTANT PROFESSOR, DEPARTMENT OF COMPUTER, SRI KRISHNA ADITHYA COLLEGE OF ARTS AND SCIENCE, Sugunapuram, Kuniamuthur P.O, Coimbatore, Tamilnadu, India, Pin code - 641008.IndiaIndia

Applicants

NameAddressCountryNationality
PANDIKUMAR SASSOCIATE PROFESSOR, DEPARTMENT OF MCA, ACHARYA INSTITUTE OF TECHNOLOGY, Acharya Dr. Sarvepalli Radhakrishnan Road, BANGALORE, KARNATAKA, India, Pin code-560010.IndiaIndia
SHAHEENA KVASSISTANT PROFESSOR, DEPARTMENT OF MCA, ACHARYA INSTITUTE OF TECHNOLOGY, Acharya Dr. Sarvepalli Radhakrishnan Road, BANGALORE, KARNATAKA, India, Pin code-560010.IndiaIndia
ANILA R.NAMBIARASSISTANT PROFESSOR, DEPARTMENT OF MCA, ACHARYA INSTITUTE OF TECHNOLOGY, Acharya Dr. Sarvepalli Radhakrishnan Road, BANGALORE, KARNATAKA, India, Pin code-560010.IndiaIndia
MUDASSER RASHIDASSISTANT PROFESSOR, DEPARTMENT OF MCA, ACHARYA INSTITUTE OF TECHNOLOGY, Acharya Dr. Sarvepalli Radhakrishnan Road, BANGALORE, KARNATAKA, India, Pin code-560010.IndiaIndia
C M SULAIKHAASSISTANT PROFESSOR&HEAD, DEPARTMENT OF COMPUTER, MTM COLLEGE OF ARTS,SCIENCE AND COMMERCE Street Pazhanji, Veliancode - Maranchery Rd, VELIYANCODE, KERALA, India, Pin code- 679578.IndiaIndia
ARUN M .ASSISTANT PROFESSOR, DEPARTMENT OF COMPUTER, SRI KRISHNA ADITHYA COLLEGE OF ARTS AND SCIENCE, Sugunapuram, Kuniamuthur P.O, Coimbatore, Tamilnadu, India, Pin code - 641008.IndiaIndia

Specification

FORM 2
710082664
THE PATENTS ACT, 1970
(39 of 1970)
AND
THE PATENTS RULES, 2003
COMPLETE
SPECIFICATION
(See Section 10; rule 13)

Assessment of High-Dimensional Data Classification for Skin Malignancy Detection Using Deep Learning Techniques * . ~ '
FIELD OF INVENTION
Malicious red lumps with a firm structure that develop into ulcers where these patches appear scaly and flat in the skin These tend to develop the mutations that can occur in the DNA of skin cells. These mutations can cause abundant growth, which produces a wide range of cancer cells. Skin cancer can also be caused by prolonged exposure of skin cells. These skin cancers are at high risk, which spreads the features based on carcinoma. This advanced ' melanoma uses imaging tests with a lymph node biopsy to identify whether those cancers get affected within the body. This cancer treatment can leave scars that look similar to those skin lesions. The life cycle of skin cells accumulates over the skin's surface due to prolonged exposure to UV rays. Skin cancer determines whether melanoma can develop anywhere within the body, indicating normal skin or cancerous skin.

TITLE OF THE INVENTION
Assessment of High-Dimensional Data Classification for Skin Malignancy Detection Using Deep Learning Techniques

APPLICANT
The following specification particularly describes
the invention and the manner in which it is to be performed

FIELD OF INVENTION
Malicious red lumps with a firm structure that develop into ulcers where these patches appear scaly and flat in the skin These tend to develop the mutations that can occur in the DNA of skin cells. These mutations can cause abundant growth, which produces a wide range of cancer cells. Skin cancer can also be caused by prolonged exposure of skin cells. These skin cancers are at high risk, which spreads the features based on carcinoma. This advanced ' melanoma uses imaging tests with a lymph node biopsy to identify whether those cancers get affected within the body. This cancer treatment can leave scars that look similar to those skin lesions. The life cycle of skin cells accumulates over the skin's surface due to prolonged exposure to UV rays. Skin cancer determines whether melanoma can develop anywhere within the body, indicating normal skin or cancerous skin.

According to each and every type of skin cancer, the warning signs are difficult. This skin cancer develops as a result of uncontrollable DNA mutations, which result in a large number of cancer cells. The primary goal of those cancer prevention trials, which include numerous clinical trials, is to identify the actions that people may take in order to develop cancer(Arun 2022). One of the most important aspects of skin cancer prevention is recognising potentially cancerous skin changes and alerting the physician to any suspicious lymph nodes. The trained neural network can improve overall performance over the accuracy rate and system performance for diverse sets of datasets with a wide range of class variability. Figure 1 represents the different skin malignancy classification. Analyzing the lesion image at an early stage, which highlights the model appropriately., Aggregating the new data techniques considerably increases the accuracy based upon the.diversity, which trains the images using augmentation where these models are robust, which in turn increases the testing accuracy.

It is primarily used to identify'skin cancer and distinguish benign skin cancer from melanoma based on lesion parameters such as structure, composition, symmetry, size, and color. Skin cancer techniques collect relevant information using a deep-neural approach, which is then ' trained to classify the images. Classify images assembles the set of images used for image recognition. Skin lesion classification relies on small datasets with limited diversity. A variety of images comprise unbalanced datasets that pre-process and detect the lesion using automated skin detection where the lesion images are cancerous.

ART OF INVENTION
I
High-Dimensional Data
In this DL approach, feature extraction and classification of those lesion images are performed. The initial state of data augmentation tends to augment those images. CNN was used to extract that information, such as image contrast and the location of the lesion's boundary. By performing skin lesion detection, it attains more accurate results than going for PET scans and biopsies. Clinical images obtain the skin disease from those images, which are obtained from the medical records of those patients. Clinical images include morphological features, which considerably handle the inaccuracies within those diagnostic results. An automatic diagnostic system analyses high-dimensional quality images of skin lesionsi.e., Figure 6 denotes proposed architectural diagram. Physicians rely on high-resolution images, which focus on the observation of those image pixels. High-quality dermatological images and analyses focus on clinical diagnosis. Skin cancers, which perform with fine-grained classes such as melanoma classification, are divided by fine-grained composition structure. From the experiments, skin cancer classification attains those diagnostic levels, which are equivalent to those dermatologists' conclusions. These data imbalances and limitations are considered the main factors in skin classification tasks.

Unwanted noise refers to image features that contain artefacts that may interfere with the desired accuracy. Unwanted noise contains artefacts that must be eliminated, such as low contrast, low brightness in those neighbouring tissues, texture colour imbalance, and image reflections, which can damage the accuracy of those skin-lesions,-respectively.-Within the- human body, moles are difficult to identify as benign (normal) or malignant. Image preprocessing interprets the structure of those cancerous lesions. Extracting those segmented medical images reveals those medical areas within the research. Because of the large datasets used to annotate the skin lesion images, models tend to over fit.

PROPOSED METHODOLOGY
Data Pre-Processing
In this image pre-processing step, the initial stage is to improve the overall image quality of those images by removing those irrelevant sets of noise and any unwanted regions within the background skin images. In this paper, it mainly gathers up those.pre-processing steps that can be used for skin lesion images. These melanoma parameters characteristics focus on the size, color, symmetry, and shape of those image segmentations, as well as their features, in this skin lesion analysis approach. These extracted sets of features classify the images and identify normal-type skin and melanoma-based skin/ Lesion image analysis examines various melanoma parameters such as asymmetry, color, and image segmentation with feature stages. These parameters classify the image as normal skin or melanoma skin in this extracted feature.

High-quality diagnostic tools are used to revitalise those medical sectors that save human lives by detecting cancer at an early stage of malignant changes. This mainly applies to the limitation in detecting those abnormal noises; which enhance the.quality of those original images. One of the main purposes is to improve the melanoma image quality by removing unrelated and other background noise for further image processing. Only a good selection of pre-processing steps will improve the accuracy of the system model where figure 2 and 3 indicates data preparation in training and testing set.

Image.name
patlent id
SCX
age.approx
anatom_site_general_cha1lenge
diagnosis
benign.matignant
target
0
ISIC.2637011
tP_7279968
male
45.0
head/neck
unknown
benign
0
1
ISIC.0015719
IP.3O75186
female
45.0
upper extremity
unknown
benign
0
2
ISIC_OO52212
IP.2342074
female'
50.0
lower extremity
nevus
benign
0
3
fSIC_0068279
IP.6890425
female
45.0
head/neck
unknown
benign
0
4
ISIC.0074268
IP_8723313
female
55.0
upper extremity
unknown
benign
0
Figure 2: Processed Data Preparation - Training
image name
patient.id
sex
age_approx
anatom_slte_general_challenge
diagnosis
benign.malignant
target
0
ISIC-2637011
!P_7279968
2
45.0
1
unknown
benign
0
1
ISIC.0015719
IP-3075186
1
45.0
------ 7
unknown
, ' benign
0
2
ISIC_0052212
IP.2842074
1
50.0
2
nevus
benign
0
3
ISIC_0068279
IP_6S9042S
1
45.0
' 1
unknown
benign
0
4
tSIC_0074268
IP_8723313
1
55.0
7
unknown
benign
0
Figure 3: Processed Data Preparation - Testing


Data Extraction

Skin melanoma detection classifies different skin cancers using a high-tech diagnostic process using different scanners, which provides the precision data that aids the doctors in monitoring and managing patients. Physicians forecast which cancers will progress before or after treatment. Traditional methods of extracting data from patient-specific information are incapable of identifying the exact affected parts of the body. Data extraction identifies the skin cancers, and high-tech imaging devices provide additional precision data by extracting those images accordingly. Using the deep CNN, the images are recognised with greater accuracy and a wider range of memory.

Data Segmentation
Skin cancer acquires the images, image pre-processing, and segmentation df images by determining those lesions. In this deep learning technique, skin lesion segmentation tends to segment those images that have pigmented lesions. Figure 3 denotes the benign and malignant state in the high-dimensional dataset. In this mode, it reduces the dimension of colour image intensity and almost handles that intensity threshold. It also redefines image segmentation with image edges. With semantically interpretable objects, DL classifies those identities in images into one or two classes. DL classifies each pixel with two classes provided from real-object categories. In this algorithm, it preserves the dermoscopy image appearance with neighbouring pixels. By cleaning up those images in morphological analysis, which preserves their structural composition, these preserve the structural properties that quantify those geometrical structural aspects of images.

Each part of the image is processed in a morphological state, where the evaluation metrics are performed using segmentation steps that extract with high precision, recall, sensitivity, and selectivity. Skin lesion segmentation tends to achieve the image-guided surgical approach, and both non-lesion regions and lesion regions are segmented.

Data augmentation tends to expand those datasets by identifying those oversampling images
and retaining their original pixel size. The ISIC dataset is made up of skin cancer data from nine different classes, with images sorted by classification. The dataset consists of different
melanoma disease classifications taken from ISIC. Analysis reveals the significant number of
duplicate images within those datasets.

Melanoma Cells
Melanoma is a serious form of cancer that develops on the cells that produce melanin. Melanin pigment gives skin colour (pigmentation, which develops on the skin layer). By limiting sun exposure, the melanin pigmentation can be reduced. They are generally found on the basal layer of the epidermis. Melanocytes are the cells involved here. A squamous cell tumour is'an aggressive tumour, and it is responsible for 90% of skin cancer mortality. The discovery of mutations in melanoma calls for better treatment when those melanocytes grow out of control. Melanocytes produce melanin, which explains why these tumours are brown or black in color. Melanomas can appear anywhere on the skin membranes of the human body's neck or face. Melanoma spreads rapidly all over the body in several body parts, such as the mouth, neck, eyes, and genital parts of the body.

atypical ntdanucyticpiolifeiutkNi cale-au-lait macule aolar lantigo lichenoid keratosis
lentigo NOS
sebontieic keratosis

ntJajHJitia |
nevus
unknown
0 5000 10000 15000 20000 25000
Figure 7; Different Skin Melanoma Types

DL Technique
The deep learning detects the dermoscopy images, where the images include melanoma and non-melanoma cancers. This proposed paper achieves high performance in distinguishing between benign and malignant lesions. The active state is classified as an early diagnosis based on unstructured data analyses of a wide range of data. The deep learning approach achieves high accuracy and other statistical characteristics. A large number of patient records and data collection, resulting from personalised treatments, where the automated way of analysing health information is used. In this DL model, detection of skin cancer is based on the dermoscopy images. DL transforms patient care, which is its primary role in clinical practice. The complex analyses where the abnormality is determined are simplified by DL algorithms. CNN accurately informs medical professionals about their patients' medical issues. DL improves interpretability, allowing for a better understanding of biological data. Using the fundamentals of deep learning mechanisms, we can cluster data and predict with high accuracy. CNN provides medical professionals who notice health problems in their patients. Medical professionals discover deep learning-insights by discovering data that serves the healthcare industry. In healthcare, DL provides more accurate disease analysis results in medical decisions. DL enables continuous monitoring by trailing out the minimum state of errors and making human intervention easier

We Claim
1. These persistent skin lesions do not heal properly, which causes a suspicious state of malignancy that has to be examined by a physician.

2. Early diagnosis and treatment reduce the highly favourable state of the prognosis. Mutations enable those abnormal cells (cancer cells), which don't give any normal signals and divide continuously.

3. DL models characterise the actual images that are pre-processed, limiting their potential categorization. These cancerous cells invade the body by interfering with normal body functions.

4. Mutations within the DNA cells can easily damage those cellular cells. The classification of skin malignancies is determined by considering the various comparative analyses.

5.The classification approach is used to identify the distinct phases of skin malignancy classification, including precision, specificity, Fl-recall, and sensitivity in deep learning approaches.

Documents

NameDate
202441082149-Correspondence-281024.pdf01/11/2024
202441082149-Form 1-281024.pdf01/11/2024
202441082149-Form 2(Title Page)-281024.pdf01/11/2024

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