The landscape of genetic disease diagnosis has seen unprecedented advances in recent years. Accuracy and speed in detecting hereditary pathologies is now a matter of days and even hours, thanks to the sophistication of genetic tests.
One of the great achievements in this field is next-generation sequencing (NGS), a technique that allows for the simultaneous analysis of thousands of genes associated with genetic diseases. This has made it possible to identify mutations in rare diseases that were once difficult to diagnose. Also notable are gene panels, in which specific groups of genes related to a pathology or group of pathologies are analyzed. This analysis enables the diagnosis of complex genetic diseases such as Lynch Syndrome or muscular dystrophy.
The era of customization: Predictive genomic medicine
Parallel to the detection of hereditary diseases, predictive genetic diagnostics are positioned as another of the great advances. These tests identify genetic variants that can predispose an individual to developing diseases and can help predict the response to certain medications. We are talking about personalized medicine, a medicine designed to fit our genomic information.
Advances in artificial intelligence and machine learning are revolutionizing genetics, especially in the interpretation of genomic data. The volume of information handled in genomic sequencing is enormous, and artificial intelligence helps to achieve a faster and more accurate analysis. Additionally, it enhances the detection of patterns and the prediction of diseases.
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On our platform, you’ll find an interactive space where you can stay up-to-date with the latest technological and scientific advances in the sector. You’ll have access to a directory of specialized laboratories, you can design your profile, make contacts, and explore opportunities in more than ten languages. Imagine having your own 3D lab, where you can post to buy, sell, or rent lab or medical equipment.
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