Recent advances in DNA sequencing technology have made it possible to uncover new methods of understanding our genetic code. In a new study, published in Nature Genetics, researchers from the University of California San Diego (UCSD) have developed a new method of DNA sequencing that can be used to uncover genetic variations between individuals. This method, known as “High-Fidelity Readout” (HFR), is a powerful tool that can detect even the smallest genetic mutations that are often overlooked. The new method is already being used to study the genetic basis of diseases such as cancer and Alzheimer’s. HFR has the potential to uncover genetic variations that could lead to new treatments and therapies. This is an exciting development in the field of genetics and could have far-reaching implications for our understanding of human health and disease.

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source: Phys.org