Nebula Genomics customers get access to the Nebula Library, a weekly updated collection of personalized reports based on the latest genetic discoveries. It empowers our users to stay up to date with the latest research in human genetics and learn how it applies to them. Today, the Nebula Library includes over 200 genome-wide association studies (GWAS) and new reports are added every week. To access your personalized Nebula Library, you need to purchase our Whole Genome Sequencing (or upload existing DNA data to get partial access). However, we also made the content of the Nebula Library publicly available here to help you discover reports that interest you.
STUDY TITLE: Large-scale genotyping identifies 41 new loci associated with breast cancer risk SUMMARY: 41 novel genetic variants were determined to be associated with breast cancer, most of which are found in genes that play a role in cell death …
STUDY TITLE: Common variants at 11p13 are associated with susceptibility to tuberculosis SUMMARY: Resistance to tuberculosis may be associated with a genetic variant in the WT1 gene. DESCRIPTION: Tuberculosis is a disease caused by bacteria that usually affect the lungs, …
STUDY TITLE: Genome-wide association study identifies five susceptibility loci for glioma SUMMARY: Identification of 5 risk variants associated with the development of gliomas. OVERVIEW: Glial cells are found in the brain, spine, and other parts of the nervous system. The …
STUDY TITLE: Identification of an emphysema-associated genetic variant near TGFB2 with regulatory effects in lung fibroblasts SUMMARY: Genetic variants near the TGFB2 gene may increase the risk of emphysema by elevating TGFB2 expression in lung fibroblasts. DESCRIPTION: Emphysema is one …
