Home » News » New ia decipher hidden genetic combinations that cause complex diseases such as cancer and diabetes

New ia decipher hidden genetic combinations that cause complex diseases such as cancer and diabetes

Breaking News: AI Revolutionizing Disease Treatment with New Genetic Tool

June 11, 2023 — MADRID — In a groundbreaking development that promises to revolutionize the treatment of complex diseases like diabetes, cancer, and asthma, researchers from Northwestern University have unveiled an AI computational tool designed to identify combinations of genes responsible for these conditions.

Understanding the New AI Tool in Disease Research

Unlike single-gene disorders, complex diseases are influenced by multiple genes working in concert. The sheer number of possible genetic combinations makes pinpointing the genes involved a daunting task for researchers. However, Northwestern University’s AI generative model amplifies limited gene expression data, helping scientists uncover patterns that correlate with disease development.

The potential implications are vast. This new information could lead to personalized treatments targeting multiple genes, marking a significant advancement in medical practice.

Expert Insight on the Breakthrough

“Many diseases are determined by a combination of genes, not just by one,” says Adilson Motter, lead author of the study. “Our model simplifies the process by identifying key factors and their collective influence.”

After decades of research, scientists now understand that non-pathological traits like height and intelligence also rely on gene sets rather than single genes. methods, like full-genome association studies, often lack the statistical power to detect the collective effects of gene groups.

The Promise of Personalized Medicine

The model, called TWAVE, uses AI to identify genetic patterns from limited data. It emulates disease states to correlate genetic expression changes with observable traits in patients. Instead of focusing on individual genes, TWAVE pinpoints groups of interacting genes.

The study, published in ‘PNAS’ (Proceedings of the National Academy of Sciences), showcases the efficacy of the TWAVE model. It successfully identified genes causing diseases that other methods missed, revealing that different gene sets can cause the same disease in different people.

Future Outlook and Practical Uses

Environmental factors influence gene expression without altering DNA sequences. This advantage allows researchers to consider these factors indirectly, enhancing the relevance of the TWAVE model.

This breakthrough opens the door for personalized medicine, where treatments can be tailored to individual patients based on their specific genetic factors. In the future, personalized treatments tailored to each patient’s genetic makeup could be the norm rather than the exception.

“A disease can manifest in a similar way in different people,” says Motter, “But different sets of genes could be involved due to genetic, environmental, and lifestyle differences.”

You may also like

Leave a Comment

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Adblock Detected

Please support us by disabling your AdBlocker extension from your browsers for our website.