Machine Learning Prognostics for Genetic Disorder Prediction

By improving the precision of genetic abnormality diagnosis and prediction, machine learning is transforming healthcare and creating opportunities for personalized treatments and early intervention. This research explores the application of machine learning methodologies in the analysis of patient medical records and large genomic datasets for genetic disease prediction. The technology correctly diagnoses hereditary disorders such as Huntington’s disease, muscular dystrophy, and cystic fibrosis through complex approaches such as neural networks, decision trees, and support vector machines. By integrating crucial elements such as genetic mutations, family medical history, and environmental factors, the framework efficiently evaluates possible genetic hazards. This creative approach facilitates the implementation of individualized treatments and preventive healthcare measures, which reduces the load on medical resources while improving patient care. The project highlights how revolutionary data-driven.

Authors

Institutions

Publication Details

Published
2025-03-05
DOI
https://doi.org/10.1109/esci63694.2025.10988005
Citations
1
Primary Topic
Genetics, Bioinformatics, and Biomedical Research
Type
article
Field-Weighted Citation Impact
0.81
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Machine Learning Prognostics for Genetic Disorder Prediction

C B Rajesh, Lakshmi Puzhankara, P Vasanth, B Santhosh Kumar et al.
1 citations
Genetics, Bioinformatics, and Biomedical Research
0.81
article

Machine Learning Prognostics for Genetic Disorder Prediction

C B Rajesh, Lakshmi Puzhankara, P Vasanth, B Santhosh Kumar, Jayalekshmi Krishnamoorthy, E Poovannan
article en
1 citations

Abstract

By improving the precision of genetic abnormality diagnosis and prediction, machine learning is transforming healthcare and creating opportunities for personalized treatments and early intervention. This research explores the application of machine learning methodologies in the analysis of patient medical records and large genomic datasets for genetic disease prediction. The technology correctly diagnoses hereditary disorders such as Huntington’s disease, muscular dystrophy, and cystic fibrosis through complex approaches such as neural networks, decision trees, and support vector machines. By integrating crucial elements such as genetic mutations, family medical history, and environmental factors, the framework efficiently evaluates possible genetic hazards. This creative approach facilitates the implementation of individualized treatments and preventive healthcare measures, which reduces the load on medical resources while improving patient care. The project highlights how revolutionary data-driven.

Saveetha University (IN)
Openalex Percentile: Top 28%
Genetics, Bioinformatics, and Biomedical Research
0.81
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.