APExBIO’s whole genome sequencing (WGS) detects the complete genome sequence at one time and provides the most comprehensive collection of an individual’s genetic variation based on the reference genome, and analyzes the differences of individuals or groups. By this way, we can obtain a lot of genome information, such as SNP, InDel, LOH, CNV and SV.
WGS can be applied to genetics and evolution studies to detect genome-wide genetic variations, pathogenic and susceptibility genes, and to enable genetic diversity and evolution analysis. It can also be applied to translational research to provide information on cancer and disease-associated mutations and is one of the most important approaches of precision medicine.
Whole Genome Sequencing