Whole Genome Sequencing (WGS) is a cutting-edge technology that offers a complete and detailed view of an organism’s genetic makeup. By analyzing an organism’s full DNA sequence, WGS provides unmatched insights into genetic variations, disease predispositions, and microbial identification. Whether advancing medical research, improving healthcare, or ensuring the quality and safety of microbial strains, WGS is transforming our understanding of biology at a fundamental level. The data produced by WGS is driving innovation across research, clinical applications, and beyond.
With rapid technological advancements continually reducing sequencing costs, WGS has become an essential tool in genomics research. It provides a high-resolution, base-by-base view of the genome, detecting both large-scale and subtle genetic variations that might be missed by more targeted approaches. WGS also supports the discovery of gene regulation mechanisms and enables the rapid generation of data for assembling and analyzing novel genomes.