Long-read sequencing

Long-read sequencing is a technology that allows scientists to read large segments of DNA information all at once, often thousands to millions of base pairs long. Unlike traditional methods that read smaller pieces and then assemble them, long-read sequencing captures continuous, longer stretches directly. This improves accuracy in identifying complex genetic structures, such as repetitive regions or structural variations, making it especially useful for studying genomes with high complexity. It helps researchers better understand genetic information, which can aid in disease research, personalized medicine, and evolutionary studies.