About us
We provide an integrated knowledge base dedicated to advancing public health genomics and human genome epidemiology. Through our carefully curated resources, tools, and databases, we aim to facilitate the exploration of genetic associations, epidemiological trends, and genomic discoveries that inform precision public health initiatives.
Our platform supports researchers, clinicians, and policymakers by providing access to comprehensive data on genetic associations, disease pathways, and genotype prevalence. Tools like the HuGE Navigator, Phenopedia, and GWAS Integrator enable detailed analyses of genomic information, while specialized databases, including the Health Impact Scan and CDC-Authored Genomics Publications, deliver insights grounded in robust scientific evidence.
With a commitment to advancing genomic research and its applications, we invite you to explore this resource, engage with the data, and contribute to the field of human genome epidemiology.
