The order of nucleotides throughout the genome can be determined using Next Generation Sequencing (NGS), a massively parallel sequencing technique that offers scalability, ultra-high throughput, and fast speed. One of the most crucial steps in the entire sequencing methodology is DNA pre-sequencing, which entails preparing the material for the subsequent sequencing reaction. Globally, clinical laboratory analysis, testing, and illness diagnosis in the healthcare industry are incorporating NGS more and more. Next-generation sequencing (NGS) is frequently utilised in pharmacogenomic to expedite the drug discovery process.
The field of molecular biology and genomics has been completely transformed by NGS, sometimes referred to as deep sequencing and parallel sequencing. It is a non-Sanger based, high throughput sequencing technique. Genome sequencing is now relatively quick and inexpensive because to Next Generation Sequencing. This approach effectively sequences billions of DNA strands. The convenience of whole genome sequencing and the examination of diverse DNA-protein interactions have been made available by next generation sequencing. The researcher can concentrate on, examine, and interpret deep sequence target regions using this method.
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