Two Main Gene Discovery Methods Reveal Complementary Aspects of Biology
The two main approaches for discovering disease genes reveal distinct aspects of biology, a new study shows. Although both methods are widely used, the research found that they identify different genes, with major implications for drug development. Published online November 5 in Nature , the study revolves around the human genome, which contains thousands of genes that provide instructions for making proteins, as well as regulatory DNA that controls when genes turn on. The new investigation takes a genome-wide view of how small DNA differences—called variants—can influence traits such as height, hair color, and disease risk. Led by researchers at NYU Langone Health; Stanford University; University of California, San Francisco; and the University of Tokyo, the new work analyzed two main methods used to determine how genetic differences influence disease biology. These are genome-wide association studies (GWAS), which test common variants across the genome—in genes and regula...