Next-Generation Sequencing (NGS) is a high-throughput DNA sequencing technology that allows rapid and cost-effective analysis of large genomes. Unlike traditional Sanger sequencing, NGS processes millions of DNA fragments simultaneously, enabling whole-genome, exome, transcriptome, or targeted sequencing.

Key Features of NGS:

• Massively Parallel Sequencing – Enables sequencing of billions of DNA fragments at once.

• High Speed & Scalability – Delivers results faster and cheaper than older methods.

• Wide Applications – Used in genomics, cancer research, infectious disease studies, pharmacogenomics, and precision medicine.

• Versatility – Supports whole-genome sequencing (WGS), exome sequencing, RNA-Seq, ChIP-Seq, and metagenomics.

NGS has revolutionized biomedical research, diagnostics, and personalized medicine by providing deep insights into genetic variations, gene expression, and disease mechanisms.