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: GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty (Hearing Loss) in UK Biobank SUMMARY: Identification of 44 genetic variants associated with age-related hearing impairment. DESCRIPTION: Hearing loss is one of the most common age-associated …
Nebula Genomics DNA Report for Healthy Lung Function Is healthy lung function 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 …
Healthy Lung Function – Is Lung Function Genetic? Read More »
STUDY TITLE: A meta-analysis of genome-wide association studies of epigenetic age acceleration SUMMARY: Discovery of 10 genetic variants associated with accelerated aging. OVERVIEW: Biological age” is a measure of how well a human body is functioning relative to its actual …
STUDY TITLE: Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism SUMMARY: Identification of 116 genetic variants associated with neuroticism. DESCRIPTION: Neuroticism is a personality trait characterized by negative emotionality (e.g. anger, guilt, anxiety) and associated with …
STUDY TITLE: Genetic predisposition to mosaic Y chromosome loss in blood SUMMARY: Discovery of 156 genetic variants associated with a mosaic loss of chromosome Y. OVERVIEW: Our DNA is packed into 23 pairs of chromosomes including two ‘sex chromosomes’. Females …
STUDY TITLE: Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope (fainting) and collapse SUMMARY: Genome-wide analysis reveals a novel genetic loci correlated with syncope, or fainting. DESCRIPTION: Syncope, also known as fainting, is a temporary loss of …
Nebula Genomics DNA Report for Varicose Veins Are varicose veins 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, …
Varicose Veins (Fukaya, 2018) – More Varicose Veins Genetics Read More »
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 (Fritsche, 2015) – More macular generation genetics Read More »
STUDY TITLE: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death SUMMARY: Identification of 3 genetic variants associated with Brugada syndrome, a rare heart disorder. OVERVIEW: A healthy …
Nebula Genomics DNA Report for Glaucoma Is glaucoma 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, purchase our …
Glaucoma (MacGregor, 2018) – More Glaucoma Genetics Read More »
