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.
Nebula Genomics DNA Report for Macular Degeneration Is macular degeneration genetic? We created a DNA report based on a study that attempted to answer this question. Below you can see a SAMPLE DNA report. To get your personalized DNA report, …
Age-related Macular Degeneration (Han, 2020) – Is Macular Degeneration Genetic? Read More »
Nebula Genomics DNA Report for Hydroxyvitamin D Level Is hydroxyvitamin D level genetic? We created a DNA report based on a study that attempted to answer this question. Below you can see a SAMPLE DNA report. To get your personalized …
Hydroxyvitamin D level (Revez, 2020) – Are Hydroxyvitamin D Levels Genetic? Read More »
STUDY TITLE: The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis SUMMARY: Identification of 4 genomic regions associated with membranous nephropathy, an autoimmune disease of the kidneys. OVERVIEW: Kidneys are organs that remove waste and excess water from …
STUDY TITLE: Common variants associated with general and MMR vaccine–related febrile seizures SUMMARY: Identification of 6 genetic variants associated with febrile seizures. OVERVIEW: In small children, high fevers can induce convulsions, causing uncontrollable shaking and loss of consciousness. This condition is …
STUDY TITLE: Genetic architecture of subcortical brain structures in 38,851 individuals SUMMARY: Identification of 48 genetic loci, including 40 novel loci, associated with the brain’s subcortical volume. OVERVIEW: The brain is a complex organ made up of many regions that …
STUDY TITLE: Multivariate genome-wide analyses of the well-being spectrum SUMMARY: Novel method for multivariate traits identifies 304 genetic variants associated with well-being. OVERVIEW: Our well-being is a multivariate trait typically characterized by high life-satisfaction, positive affect, and absence of neuroticism …
STUDY TITLE: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis SUMMARY: Discovery of 41 genetic risk variants associated with allergic rhinitis. OVERVIEW: Achoo! When allergens cause inflammation in our sinuses, we begin to …
STUDY TITLE: Genome-wide associations for birth weight and correlations with adult disease SUMMARY: Identification of 60 novel genetic variants associated with birth weight and correlated with later-life disease susceptibility. OVERVIEW: Birth weight is influenced by the genetics of the mother …
Birth Weight and Disease Susceptibility (Horikoshi, 2017) Read More »
STUDY TITLE: Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness SUMMARY: Detection of 19 genetic variants associated with feelings of loneliness. DESCRIPTION: Humans are social creatures and feelings lonely arises when we don’t feel as socially connected …
STUDY TITLE: Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria SUMMARY: Genome-wide identification of 68 variants associated with albuminuria, a key indicator of chronic kidney disease. DESCRIPTION: The kidneys have an important role of filtering blood to remove wastes …
