Genomic Risk Assessment and Early Intervention for Rare Genetic Disorders

Genetic diseases pose significant challenges due to their complex nature and the need for specialized diagnostic techniques. This research focuses on developing a comprehensive framework for classifying genetic diseases using advanced machine learning algorithms. By applying techniques such as random forest classification, artificial neural networks, and support vector machines, the proposed framework aims to extract complex genetic data and accurately identify various genetic diseases. This approach empowers individuals to become more aware of their genetic health and take proactive steps for prevention and early intervention. The research contributes to the field of healthcare by providing a data-driven solution for genetic disease classification. By integrating new technologies like the chain classifier approach, the framework enhances diagnostic accuracy and addresses the complexities associated with genetic interactions. This work represents a significant step towards improving the understanding and management of genetic diseases, ultimately contributing to global health.

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Publication Details

Published
2024-09-18
DOI
https://doi.org/10.1109/icosec61587.2024.10722427
Citations
1
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.55
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article

Genomic Risk Assessment and Early Intervention for Rare Genetic Disorders

G. Kalyani, Kolla Vaibhav, Sribhashyam Sashank Sai, Namballa Ram Tarun
1 citations
Genomics and Rare Diseases
0.55
article

Genomic Risk Assessment and Early Intervention for Rare Genetic Disorders

G. Kalyani, Kolla Vaibhav, Sribhashyam Sashank Sai, Namballa Ram Tarun
article en
1 citations

Abstract

Genetic diseases pose significant challenges due to their complex nature and the need for specialized diagnostic techniques. This research focuses on developing a comprehensive framework for classifying genetic diseases using advanced machine learning algorithms. By applying techniques such as random forest classification, artificial neural networks, and support vector machines, the proposed framework aims to extract complex genetic data and accurately identify various genetic diseases. This approach empowers individuals to become more aware of their genetic health and take proactive steps for prevention and early intervention. The research contributes to the field of healthcare by providing a data-driven solution for genetic disease classification. By integrating new technologies like the chain classifier approach, the framework enhances diagnostic accuracy and addresses the complexities associated with genetic interactions. This work represents a significant step towards improving the understanding and management of genetic diseases, ultimately contributing to global health.

Siddhartha Medical College (IN)
Openalex Percentile: Top 25%
Genomics and Rare Diseases
0.55
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Genomic Risk Assessment and Early Intervention for Rare Genetic Disorders — G. Kalyani, Kolla Vaibhav, et al. · (2024) | TGRS Research Map | TGRS