Year: 2024
Type: conference-paper
Abstract: Cancer risk forecast early on is still one of the biggest problems in modern medicine. Genomics-based engineering systems could change the way cancer risks are predicted by giving individuals personalised information based on their genes. This study looks into how advanced engineering methods can be combined with genetic sequencing to create models that can predict cancer risk. We want to find specific genetic markers linked to different types of cancer by looking at big genome datasets. This will allow the creation of predictive tools that can figure out a person's risk profile. To find trends in large amounts of complex genetic data, these systems use state-of-the-art machine learning techniques, such as deep learning and feature selection methods. We also look at how bioinformatics tools can be used to process and understand genome data so that correct risk predictions can be made. The suggested engineering systems use genetic data, medical background, and external factors to make a full risk prediction model that can be used in personalised medicine. The findings of this study could help create earlier diagnosis methods, more focused ways to avoid getting the disease, and better treatment plans that are based on each person's unique genetic make-up. The goal of this study is to improve patient results and lower the worldwide impact of cancer by helping us learn more about the genetic causes of cancer. The results show that genetic engineering systems will become more important in the future for predicting, diagnosing, and stopping cancer.
Authors: T M Swathy, Aparna P Patange, Chandrayani Rokde, Dharmesh Dhabliya, Gauri Tamhankar, Uday Pratap Singh
Language: English
Subfield: Cancer Research
Domain: Life Sciences
Open Access status: hybrid
OpenAlex ID: W4413915539