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In the last couple of years, the discovery and characteri-zation of copy-number variations (CNVs) in the human genome have provided a new research tool for identifying genetic risk factors of common complex diseases, referred to as CNVs based genome-wide association studies (GWAS).
In the last couple of years, the discovery and characteri-zation of copy-number variations (CNVs) in the human genome have provided a new research tool for identifying genetic risk factors of common complex diseases, referred to as CNVs based genome-wide association studies (GWAS).