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Introduction


Whole Genome Sequencing (WGS) is applied to identify the somatic and germline mutations, structural variations, copy number variations (CNV) and SNP loci via the re-sequencing of the human genome, to 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.



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Avantages



Application Regions