Home  > Services  >  Human WGS  > Introduction

Whole Genome Sequencing (WGS) is applied to identify the somatic and germ line mutations, structural variation, copy number variation (CNV) and SNP loci via the re-sequencing of the human genome; further explore the pathogenesis, pharmacological mechanism and susceptible gene targets of disease and cancer genomes from the perspective of comprehensive application of comparative genomics, population genetics and pharmacogenomics.



Annoroad Gene Tech. (Beijing) Co., Ltd

info@genome.cn

+86 4008-986-980