  <?xml version="1.0"?>
<journal>
 <journal_metadata>
  <full_title>Fusion: Practice and Applications</full_title>
  <abbrev_title>FPA</abbrev_title>
  <issn media_type="print">2692-4048</issn>
  <issn media_type="electronic">2770-0070</issn>
  <doi_data>
   <doi>10.54216/FPA</doi>
   <resource>https://www.americaspg.com/journals/show/3807</resource>
  </doi_data>
 </journal_metadata>
 <journal_issue>
  <publication_date media_type="print">
   <year>2018</year>
  </publication_date>
  <publication_date media_type="online">
   <year>2018</year>
  </publication_date>
 </journal_issue>
 <journal_article publication_type="full_text">
  <titles>
   <title>Hybridization of Deep Learning Model with Optimization Algorithm for DNA Based Genetic Disorders Detection and Classification</title>
  </titles>
  <contributors>
   <organization sequence="first" contributor_role="author">Research Scholar, Department of Computer Science and Engineering, FEAT, Annamalai University, Chidambaram, India</organization>
   <person_name sequence="first" contributor_role="author">
    <given_name>S.</given_name>
    <surname>S.</surname>
   </person_name>
   <organization sequence="first" contributor_role="author">Associate Professor, Department of CSE, Government College of Engineering, Sengipatti, Thanjavur, India</organization>
   <person_name sequence="additional" contributor_role="author">
    <given_name>G.</given_name>
    <surname>Indirani</surname>
   </person_name>
  </contributors>
  <jats:abstract xml:lang="en">
   <jats:p>Genetic diseases are diseases produced by anomalies in the DNA of the person. These abnormalities may be larger-scale chromosomal mutations or irregularities in the particular gene. These diseases significantly influence some body functions and systems and are hereditary or develop automatically. Traditional models such as genetic testing and karyotyping might fail to identify complex or rare modifications, requesting more detailed techniques namely whole-genome sequencing (WGS). In recent decades, regardless of important technological evolution, uncommon genetic diseases continue to cause problems, with a significant portion of patients (50–66%) remaining unidentified according to clinical condition alone. An accurate analysis is important to provide equal support to patients and their relations, despite particular therapeutic intrusions. Presently, machine learning (ML), and in detail the DL subspecialties, have been utilized to determine clinically relevant prediction devices in other medical areas. For mental disorders, ML methods have presented major promise in forecasting either diagnosis or prediction in mental disorders. In this manuscript, we design and develop a Hybrid Deep Learning and Metaheuristic Optimization Algorithm for Detecting Genetic Disorders (HDLMOA-DGD) model. The proposed HDLMOA-DGD algorithm's main goal is to detect and classify genetic disorders using an advanced deep-learning model. At first, the Z-score normalization is employed in the data pre-processing phase for converting an input data into a uniform format. Moreover, the proposed HDLMOA-DGD model implements a hybrid deep learning model of the temporal convolutional network, bi-directional long- and short-term memory network, and Self-Attention mechanism (TCN-BiLSTM-SA) technique for the classification process.  At last, the modified gannet optimization algorithm (MGOA)-based hyperparameter selection process is performed to optimize the detection and classification results of the TCN-BiLSTM-SA system. The experimental validation of the HDLMOA-DGD model is verified on a benchmark dataset and the results are determined regarding several measures. The experimental outcome underlined the development of the HDLMOA-DGD model in the genetic disorder detection process.</jats:p>
  </jats:abstract>
  <publication_date media_type="print">
   <year>2025</year>
  </publication_date>
  <publication_date media_type="online">
   <year>2025</year>
  </publication_date>
  <pages>
   <first_page>77</first_page>
   <last_page>89</last_page>
  </pages>
  <doi_data>
   <doi>10.54216/FPA.200107</doi>
   <resource>https://www.americaspg.com/articleinfo/3/show/3807</resource>
  </doi_data>
 </journal_article>
</journal>
